Reticular Formation and Pain: The Past and the Future
Isabel Martins1,2,3,4 
Isaura Tavares1,2,3,4*- 1Departamento de Biomedicina, Faculdade de Medicina do Porto, Porto, Portugal
- 2Unidade de Biologia Experimental, Faculdade de Medicina do Porto, Universidade do Porto, Porto, Portugal
- 3Instituto de Biologia Celular e Molecular (IBMC), Universidade do Porto, Porto, Portugal
- 4Instituto de Investigação e Inovação em Saúde, Universidade do Porto (I3S), Porto, Portugal
The involvement of the reticular formation (RF) in the transmission and modulation of nociceptive information has been extensively studied. The brainstem RF contains several areas which are targeted by spinal cord afferents conveying nociceptive input. The arrival of nociceptive input to the RF may trigger alert reactions which generate a protective/defense reaction to pain. RF neurons located at the medulla oblongata and targeted by ascending nociceptive information are also involved in the control of vital functions that can be affected by pain, namely cardiovascular control. The RF contains centers that belong to the pain modulatory system, namely areas involved in bidirectional balance (decrease or enhancement) of pain responses. It is currently accepted that the imbalance of pain modulation towards pain facilitation accounts for chronic pain. The medullary RF has the peculiarity of harboring areas involved in bidirectional pain control namely by the existence of specific neuronal populations involved in antinociceptive or pronociceptive behavioral responses, namely at the rostroventromedial medulla (RVM) and the caudal ventrolateral medulla (VLM). Furthermore the dorsal reticular nucleus (also known as subnucleus reticularis dorsalis; DRt) may enhance nociceptive responses, through a reverberative circuit established with spinal lamina I neurons and inhibit wide-dynamic range (WDR) neurons of the deep dorsal horn. The components of the triad RVM-VLM-DRt are reciprocally connected and represent a key gateway for top-down pain modulation. The RVM-VLM-DRt triad also represents the neurobiological substrate for the emotional and cognitive modulation of pain, through pathways that involve the periaqueductal gray (PAG)-RVM connection. Collectively, we propose that the RVM-VLM-DRt triad represents a key component of the “dynamic pain connectome” with special features to provide integrated and rapid responses in situations which are life-threatening and involve pain. The new available techniques in neurobiological studies both in animal and human studies are producing new and fascinating data which allow to understand the complex role of the RF in pain modulation and its integration with several body functions and also how the RF accounts for chronic pain.
Introduction
The involvement of the brainstem reticular formation (RF) in the transmission and modulation of pain is well established. A long path has been covered since the initial anatomical studies demonstrating that the RF projects to the thalamus, passing by the functional approaches showing that manipulation of the RF changes behavioral nociceptive responses and going through imaging studies in humans indicating activation of the RF in response to pain. The study of the role of the RF in pain is challenging due to anatomical and functional reasons. Anatomically, the RF is defined as an aggregation of neurons with several morphological configurations and without distinct connection pattern. Functionally, and besides the sensory component of pain, the RF is involved in a plethora of functions which include arousal, motor reactions, cardiovascular control and visceral functions. This anatomofunctional complexity of the RF deviated neuroscientists from a global study of the involvement of the RF in pain processing and most studies have been directed to specific areas of the RF. Taking into account the concept that pain control cannot be studied apart from other brain functions and also the intrinsic feature of the RF as the brain network, by excellence, it is possible that the RF represents an outstanding example of the “dynamic pain connectome” (Kucyi and Davis, 2015, 2016).
Based on our own experience in the study of the involvement of specific areas of the brainstem RF in pain transmission and modulation in animal models of pain, in this article we critically review the participation of the medullary RF in pain modulation. The medulla oblongata contains three areas of the RF from which a wide variety of data have recently been collected, namely the rostroventromedial medulla (RVM), the caudal ventrolateral medulla (VLM) and the dorsal reticular nucleus (also known as the subnucleus reticularis dorsalis; DRt). After reviewing the anatomofunctional features of the involvement of each area in pain transmission and modulation, we then discuss how the triad RVM-VLM-DRt plays a key role as a gateway to allow pain modulation from the brain to target the spinal cord, i.e., top-down modulation (Figure 1). The role of the RVM-VLM-DRt triad in pain processing is proposed as a homeostatic neuronal circuit that allows adequate body reactions in life-threatening events, such as escaping a predator or an intense acute pain (McNaughton and Corr, 2004; Mobbs et al., 2007). Additionally the triad RVM-VLM-DRt is also proposed to be involved in situations in which adequate emotional responses to pain are necessary (Craig, 2003).
Figure 1. Diagram depicting the crucial role of the medullary reticular formation (RF) triad rostroventromedial medulla (RVM)-ventrolateral medulla (VLM)-dorsal reticular nucleus (DRt) as a gateway between the brain and the spinal cord. The three components of the triumvirate are reciprocally connected in a way which allows integration of responses which are related to pain, namely cardiovascular control and motor reactions. This probably represents a phylogenetically conserved mechanism that subserves the classical “fight or flight” response, activated by acute pain. The emotional and cognitive control exerted by higher brain centers upon the RVM-VLM-DRt triad may account to explain how the emotions and attention affect pain responses. By allowing to balance inhibition and facilitation (−/+) of nociceptive transmission at the spinal cord, the RVM-VLM-DRt medullary triad provides the mechanism to decrease or increase pain. A more detailed description of the neuronal circuits involving one component of the triad—the DRt—is shown in Figure 2, namely in what concerns its brain connections and their neurochemical characterization.
Ascending and Descending Pathways
The involvement of the spinoreticulothalamic pathway as a major ascending pathway for nociceptive transmission to the brain is well established. Overall this multisynaptic pathway originated from neurons mainly located in the spinal cord laminae IV–V and VII–VIII targets areas of the medullary and pontine RF which have collaterals of the spinothalamic tract (Lu and Willis, 1999). A role for the RF as a relay to the medial thalamus has emerged and herein conferred the RF an interesting perspective as to its involvement in the motivational-affective components of pain (Willis and Westlund, 1997; Almeida et al., 2004). As to the areas of the RF directly receiving nociceptive information from the spinal cord, our research group performed extensive neuroanatomical tract-tracing studies showing that spinal neurons projecting to the VLM or to the DRt are strongly activated in response to several types of nociceptive stimuli (Tavares et al., 1993; Almeida and Lima, 1997; Castro et al., 2006).
The brainstem RF is not only targeted by nociceptive input from the spinal cord but is also actively involved in modulation of nociceptive transmission from the spinal cord. The association of the RF to descending pain modulation is almost as ancient as the discovery that the periaqueductal gray (PAG) is involved in stimulation-produced analgesia (Heinricher et al., 2009). The PAG plays a critical role in conveying the modulatory influences from higher brain centers involved in aspects of pain responses such as cognition and emotion, including the insular and prefrontal cortices and the amygdala (Tracey and Mantyh, 2007). The PAG collects the modulatory influences from these areas and uses the RVM as a relay to indirectly target the spinal cord. Another contrasting and yet important aspect of the participation of the brainstem RF in descending pain modulation derives from the direct arrival of nociceptive input from the spinal cord, namely to the VLM and DRt, described in the next section. In contrast to the RVM, which is does not receive afferents from the spinal cord, the participation of the VLM and DRt in reciprocal loops established with the spinal cord and better analyzed in the next section, allows the RF to perform a fine tuning of nociceptive signals traveling from the spinal cord to the brain.
An Important RF Triad in the Medulla Oblongata
In this section we will summarize the anatomical and functional data that support an involvement of the RVM, VLM and DRt in the transmission and modulation of nociceptive information. The specific features of each area will be outlined in each subsection according to the following organization: (i) anatomical location; (ii) connections with the spinal cord; (iii) nociceptive control; and (iv) local neurochemical systems.
The Rostroventromedial Medulla
Anatomical Location
The RVM includes the midline located nucleus raphe-magnus (NRM) and the adjacent RF in the vicinity of the nucleus reticularis gigantocellularis. In what concerns its involvement in pain modulation, these anatomical components of the RVM are frequently considered together inasmuch that local modulation techniques, such as electrical or chemical stimulation, do not allow a precise discrimination of the NRM from the adjacent RF. Rostrocaudally, the RVM extends from the pontomedullary junction to the level of appearance of the pyramidal decussation.
Connections with the Spinal Cord
The ascending projections from the spinal cord to the RVM are very scarce. The descending input from the RVM to the spinal cord is prominent and targets almost all spinal segments, reaching mainly the dorsal horn (laminae I–V) but also lamina X (Millan, 2002). As to the way in which RVM fibers are organized in spinal neuronal circuits, it was proposed that the descending input from the RVM directly targets spinal neurons involved in ascending transmission of nociceptive input (Urban and Gebhart, 1999). These data are based in the use of tract-tracing techniques and pharmacological manipulation of the spinal cord circuits. According to recent opto/chemogenetic manipulations of the RVM, another arrangement may exist namely by GABA-mediated inhibition of inhibitory spinal interneurons that presynaptically inhibit primary afferent fibers (Francois et al., 2017). This demonstrates that the new techniques used to manipulate neuronal circuits, namely optogenetic manipulation, will allow to uncover the complexity of top-down modulation.
Nociceptive Control
The involvement of the RVM as a crucial relay station from the pain modulatory actions arising from the PAG is well established (Fields et al., 1991). For comprehensive reviews see, for example Heinricher et al. (2009) and Ossipov (2012); for a recent update see Heinricher (2016). In animal studies it was shown that the RVM has a peculiar bidirectional role in pain control at the spinal cord namely by balancing inhibitory (antinociceptive) and facilitatory (pronociceptive) effects at the spinal cord. One of the best established neurobiological mechanism of bidirectional control from the RVM is the existence in the RVM of two classes of neurons. OFF-neurons are involved in pain inhibition and their electrophysiological responses pause when the animal exhibits a nocifensive behavior. On the contrary, ON-neurons are involved in pain facilitation as their electrophysiological activity increases just prior to the appearance of a nociceptive withdrawal reflex. Besides the two types of neurons, the RVM also harbors NEUTRAL neurons which exhibit an electrophysiological activity that is not related to identified animal behavior. The coexistence of antinociceptive and pronociceptive systems at the human RVM was only recently studied. This delay in evaluating the putative translational perspectives of the existence of OFF- and ON- neurons is mainly due to the limitations of imaging techniques in the study of small regions, such as the RVM. Initial imaging studies which managed to evaluate RVM activation in healthy volunteers confirmed activation of this RF region in response to nociceptive stimulation of healthy volunteers (Fairhurst et al., 2007; Eippert et al., 2009). More recently, and by using a brainstem optimized whole brain imaging protocol, it was possible to demonstrate distinct clusters of activity in the RVM of healthy volunteers, which match the antinociceptive and pronociceptive activities of OFF-and ON-neurons, respectively (Brooks et al., 2017). The translational perspectives of this recent imaging study need to be evaluated in the future, namely to analyze if activation of pronocicetive components of the RVM increases in chronic pain patients, in a manner similar to the well-established results in animal models (Carlson et al., 2007; Gonçalves et al., 2007; Silva et al., 2013).
Local Neurochemical Systems
The role of serotonin in local control of RVM neurons has been demonstrated. In fact, and besides targeting the spinal cord, serotoninergic RVM neurons have been shown to modulate the activity of RVM neurons (Potrebic et al., 1994; VanderHorst and Ulfhake, 2006). The RVM also contains opioid-sensitive neurons since the activity of OFF-neurons is activated by mu-opioid agonists whereas the opposite occurs with ON-neurons (Heinricher et al., 1992; Heinricher and Fields, 2013). The local neurochemical control appears to be more complex and involve GABA-mediated inhibition which is triggered by opioids. Local cholecystokinin receptors (CCK2) are also relevant and provide additional possibilities of a fine tuning of neurochemical control at the RVM. An additional neurochemical system was recently unraveled at the RVM. The endovanilloid system is remotely activated from the PAG since agonists of the vanilloid receptor type 1 (TRPV1) injected into the PAG induce glutamate-mediated activation of the activity of OFF neurons (Starowicz et al., 2007; Palazzo et al., 2010). The endovanilloid system at the RVM appears to be inactivated in non-noxious conditions or during acute pain (Silva et al., 2016b). The system is only activated at the RVM in situations of chronic pain, namely during neuropathic conditions (see below in “Chronic Pain as a Trigger of Neuroplasticity at the RVM-VLM-DRt Triad” Section).
The Caudal Ventrolateral Medulla
Anatomical Location
The caudal VLM is located in the ventrolateral quadrant of the caudalmost aspect of the medulla oblongata in several species including man, rat, mouse, cat and monkeys. The VLM extends from the spinomedullary junction up to the level of the rostral border of the area postrema. The caudalmost part of the VLM contains an area designated as VLMlat, which is located between the spinal trigeminal nucleus (Sp5C) and the lateral reticular nucleus (LRt) and appears to play a specific role in pain modulation (Tavares and Lima, 2002, 2007). The VLM also includes the LRt, which is a nucleus with a specific pattern of connections and has been known for its involvement in motor responses (Alstermark and Ekerot, 2013).
Connections with the Spinal Cord
The ascending projections from the spinal cord to the VLM are anatomically segregated, with the VLMlat receiving mainly afferents from the superficial dorsal horn, namely from noxious-responding neurons located in lamina I (Tavares et al., 1993). An important contingent of VLMlat-projecting neurons is located at lamina II, which appears to be a special feature of this spinofugal pathway (Lima and Coimbra, 1991; Lima et al., 1991). On the contrary, the LRt is targeted from fibers originated from deeper layers in the spinal cord, namely from laminae IV–V, which specifically terminate in the lateral part of the LRt, and from lamina VII which terminate at the medial part of the nucleus (Lima and Coimbra, 1991; Lima et al., 1991).
Our research group performed several anatomofunctional studies to evaluate the areas of termination of descending pathways from the VLM to the spinal cord, taking into account the anatomical segregation reported above as to the spino-VLM pathway. The descending VLMlat-spinal pathway targets lamina I, IV–V and X and appears to course through the dorsolateral funiculus (Tavares and Lima, 1994; Tavares et al., 1996). A reciprocal loop between lamina I and the VLMlat was further characterized at the ultrastructural level (Tavares and Lima, 2002). Terminal boutons from lamina I establish mainly asymmetrical contacts with VLMlat neurons that project to the spinal cord, suggesting that the ascending input from the spinal cord directly activates VLMlat neurons. In the spinal cord, descending projections from the VLMlat establish both asymmetrical and symmetrical synapses (Tavares and Lima, 2002). Collectively the data suggest that the arrival of noxious input from the spinal cord triggers activation of VLMlat neurons. Detailed electrophysiological mapping of the VLM has shown that it harbors inhibitory neurons (OFF-like neurons) along with excitatory cells (ON-like cells; Pinto-Ribeiro et al., 2011) which, along with our ultrastructural data (Tavares and Lima, 2002), indicates that the descending modulation from the VLM may include facilitatory modulation, along with the well-established inhibitory effects.
Nociceptive Control
The anatomical data reviewed above are easy to conciliate with functional findings showing that the magnitude and duration of behavioral nociceptive responses is more intense when the VLMlat is stimulated (Gebhart and Ossipov, 1986) in comparison with stimulations directed to more medial VLM areas. The VLMlat contains neurons that respond to noxious activation of the joints (Pinto et al., 2007). Incidentally, it must be noted that the magnitude of activation of VLMlat neurons, as measured by the expression of the c-fos protooncogene, is directly correlated with the magnitude of activation of lamina I neurons (Pinto et al., 2006), which reinforces the functional relevance of the above mentioned lamina I-VLMlat-lamina I loop. Recent studies showed that VLMlat neurons respond to diffuse noxious stimulation of the muscles (Panneton et al., 2015) and a new role for the VLMlat as a component of the classical spinoreticulothalamic pathway has emerged in which this RF region is proposed to have a key relay role. The poor activation of more medial components of the VLM, namely the LRt, in response to noxious stimulation along with the role of the LRt in motor control suggests that the VLM may be specially positioned to provide an integrated response to an acute stimulus, namely to the classical “fight or flight” response. In fact, a recent study proposed that the spino-LRt-cerebellar pathway provides an adequate motor response in response to noxious peripheral stimulation (Huma et al., 2015). An additional component of this response involves cardiovascular parameters. The VLMlat is activated in response to increases in blood pressure (Tavares et al., 1997a; Lima et al., 2002). Increases in blood pressure are also a feature of the “fight or flight” response. Collectively, the data suggest that the VLM is an integrative center which is involved in producing the adequate pain, motor and cardiovascular responses necessary to face threatening events.
Local Neurochemical Systems
The local neurochemical circuits relevant to control the functions of the VLM in pain modulation appear to involve noradrenaline and angiotensin II. As to the former, administration of noradrenaline or the α2-adrenoreceptor agonist clonidine into the VLM inhibit local neurons and produce hyperalgesia (Cahusac and Hill, 1983; Ossipov and Gebhart, 1986). Angiotensin II injected into the VLM also induces hyperalgesia which is mediated by local angiotensin type 1 receptors (AT1 receptors; Marques-Lopes et al., 2010). By a selective manipulation of the noradrenergic projections from the pontine A5 noradrenergic cell group to the VLMlat, it was proposed that VLMlat neurons expressing AT1 receptors activate A5 noradrenergic neurons which will inhibit nociceptive transmission at the spinal cord. That triggering action of the VLM is inhibited by collaterals of the descending A5-spinal pathway (Tavares et al., 1997b). Another important neurochemical control system at the VLMlat is mediated by opioids. At the VLM, μ-opioid receptors are expressed mainly by VLMlat neurons that do not project to the spinal cord (Pinto et al., 2008b) and overexpression of opioids at the VLM induces antinociceptive effects (decreased behavioral nociceptive responses) and lower nociceptive spinal neuronal activation (Martins et al., 2011).
The Dorsal Reticular Nucleus
Anatomical Location
The DRt is located in the caudal-most aspect of the medulla oblongata in several species including man, rat, cat and monkey. The DRt extends from the spinomedullary junction up to the level of the rostral border of the area postrema. It confines with the cuneate nucleus and the nucleus of the solitary tract (NTS), dorsomedially, the Sp5C, laterally and the VLM, ventrally (Andrezik and Beitz, 1985; Newman, 1985).
Connections with the Spinal Cord
In what concerns the connections with the spinal cord, our research group has shown that DRt neurons are reciprocally connected spinal lamina I neurons forming a reverberative nociceptive circuit (Figure 2). The DRt receives bilateral projections from spinal cord laminae I, IV–VII and X with an ipsilateral predominance of those originated in the dorsal horn (Lima, 1990; Villanueva et al., 1991). Spino-DRt pathways travel though the dorsal columns, with the projections originated in the superficial dorsal horn traveling through the dorsal funiculus and those originated in the deep dorsal horn traveling in the dorsolateral fasciculus (Lima, 1990; Almeida et al., 1995; Lima and Almeida, 2002). The lateral aspect of the ventrolateral quadrant also constitute an ascending tract used by spino-DRt pathways, most likely originated from the deep dorsal horn, since lesions including the most lateral parts of the ventral funiculus prevented the activation of DRt neurons, contrary to lesions including the dorsal funiculus where fibers originated from superficial dorsal horn neurons run (Bing et al., 1990). DRt neurons project to the superficial and deep dorsal horn (Bernard et al., 1990; Tavares and Lima, 1994; Villanueva et al., 1995). DRt-spinal pathways reach the spinal cord through the dorsolateral funiculi (Villanueva et al., 1995).
Figure 2. Diagram depicting the DRt connections with the spinal cord and several brain areas. The DRt is involved in a feedback reciprocal loop with the spinal cord (thick orange lines) which is involved in pain facilitation. Through its projections to the lateral ventromedial thalamus the DRt participates in a reticulo-thalamo-cortical ascending nociceptive pathway (thick black lines). The DRt receives afferent inputs from: (i) higher centers namely the anterior cingulate cortex (ACC), the motor (Mot), somatosensory (Som) and insular (Ins) cortices, the hypothalamus (Hyp) and the amygdala (Amy); and (ii) several brainstem areas namely the periaqueductal gray (PAG), the locus coeruleus (LC), the A5 noradrenergic cell group along with the two components of the medullary triad (RVM and VLM). The DRt is a major relay for descending pain facilitatory inputs from the ACC, the Hyp and the noradrenergic LC and A5 areas. The neurochemical characterization of DRt afferents showed that afferents originated in the Mot, Som and Ins cortices as well as the Hyp and the Amy are GABAergic (GABA; thick purple lines). Hyp afferents and brainstem afferents located at the RVM and the A5 area are enkephalinergic (ENK; thick blue lines). The LC and the A5 noradrenergic cell group constitute the main source of noradrenaline (NA; thick red lines) released at the DRt. A peculiar reciprocal network is established between the DRt and the medial medullary RF (mMRF) through collaterals (green lines) of spinally descending axons. Such an arrangement was described in the cat and is thought to be involved in noxious sensing and nocifensive behavior. Blue thin lines represent neurochemically uncharacterized DRt afferents and dashed lines represent DRt or mMRF efferents.
The termination of DRt neurons in the same laminae containing spinal neurons projecting to the DRt predicts the existence of reciprocal circuits between the spinal cord and the DRt. A reciprocal excitatory loop between the DRt and superficial dorsal horn neurons was demonstrated. At the superficial dorsal horn, excitatory contacts, demonstrated at the ultrastructural level, occur between DRt descending fibers impinging upon lamina I neurons, which project back to the DRt. At the DRt, excitatory contacts were also demonstrated between fibers ascending from spinal lamina I neurons and local neurons (Almeida et al., 1993, 2000). Lamina I neurons projecting to the DRt convey nociceptive inputs to the DRt as they express c-Fos, a marker of spinal neuronal nociceptive activation (Hunt et al., 1987), upon noxious stimulation (Almeida and Lima, 1997). This reciprocal excitatory loop likely forms a reverberating circuitry feeding both the spinal cord and the DRt with nociceptive information and ultimately amplifying it. The deep dorsal horn and the DRt are also likely linked by reciprocal links as suggested by anatomical and electrophysiological data. The latter showed that activation of the DRt by glutamate injection exerts excitatory influences on deep dorsal horn neurons as observed by the long lasting increase of the responses of wide-dynamic range (WDR) neurons to noxious electrical stimulation of the sciatic nerve (Dugast et al., 2003). On the contrary, blocking the ipsilateral DRt by lidocaine produces an immediate decrease of C-fiber-evoked responses to sciatic nerve stimulation postdischarge activity of WDR neurons (Lima and Almeida, 2002).
Nociceptive Control
The DRt has been assigned a peculiar role in pain processing, with most data gathered in the rat and cat. In humans, the recent developments of functional magnetic resonance imaging (fMRI), allowing to investigate more accurately the spinal cord as well as the brainstem, also confirm the involvement of the DRt in pain processing (Rempe et al., 2014, 2015; Youssef et al., 2016). Electrophysiological in vivo recordings performed in the rat identified two neuronal subpopulations at the DRt, total nociceptive convergent neurons which are exclusively activated by noxious stimuli conveyed by Aδ- and C-fibers from the entire body, and partial nociceptive convergent neurons, which are activated by both noxious and innocuous stimuli and are targeted by C-fibers innervating only restricted areas of the body and by Aδ-fibers originated in extensive peripheral areas (Villanueva et al., 1988, 1989). In addition to responding to and encoding cutaneous and visceral noxious inputs, DRt neurons responded in a manner proportional to the intensity of stimuli (Villanueva et al., 1989; Roy et al., 1992). These electrophysiological properties were also found in DRt neurons of the monkey (Villanueva et al., 1990) and cat (Soto et al., 2008). Recent electrophysiological in vivo and in vitro studies performed in the cat and the rat, respectively, showed that a large fraction of DRt neurons presented spontaneous activity (Soto and Canedo, 2011; Sousa et al., 2014). Additionally, DRt neurons show windup (Villanueva et al., 1988), a phenomena that consists of a gradual build-up in neuronal excitability, generated in response to low frequency C-fiber afferent input or generated supraspinally (Soto et al., 2008; Soto and Canedo, 2011). This physiological property of DRt neurons is important inasmuch as wind-up has been interpreted as a system for the amplification of pain which could lead to the development of central sensitization (Herrero et al., 2000).
The DRt facilitates acute and short-lasting inflammatory pain (Almeida et al., 1996, 1999; Ambriz-Tututi et al., 2013; Martins et al., 2013, 2015a). Stimulation of the DRt by local administration of glutamate increased nociceptive acute behavioral responses while DRt lesion by local administration of quinolinic acid had the opposite effect (Almeida et al., 1996). Chemical or electrical lesioning of the DRt decrease inflammatory pain behaviors (Almeida et al., 1999). Spino-DRt-spinal excitatory loops are likely involved in the mediation of the pain facilitatory actions observed after formalin injection since both DRt lesioning or blockade of glutamate receptors at the DRt decreases formalin-induced pain behaviors and c-Fos expression in superficial and deep dorsal horn laminae of the spinal cord (Almeida et al., 1999; Ambriz-Tututi et al., 2013).
The DRt is also involved in diffuse noxious inhibitory control (DNIC), a mechanism of top-down inhibitory control of spinal dorsal horn neurons (Bouhassira et al., 1992b). DNIC is a paradigm in which one noxious stimulus is used as a conditioning stimulus to induce reduction in pain perception by another stimulus. DNIC is triggered exclusively by a conditioning noxious stimulus, conveyed by peripheral Aδ- and C-fibers, and inhibit trigeminal and spinal convergent WDR neurons (Le Bars et al., 1979; Dickenson et al., 1980). DNIC is sustained by a complex loop, involving supraspinal structures, whose ascending and descending pathways travel through the ventrolateral and dorsolateral funiculi, respectively (Villanueva and Le Bars, 1995). Early electrophysiological and lesioning studies established that pathways originated from the DRt are involved in DNIC (Bouhassira et al., 1990, 1992a,b, 1993). It was suggested that descending inhibitory inputs from the DRt constituted a separate type of inhibitory control, and it was hypothesized that DNIC triggered from the DRt could be part of a mechanism involved in the extraction of nociceptive information by depressing background body sensory activity (Le Bars, 2002).
The DNIC inhibitory control also occurs in humans (Yarnitsky, 2010; van Wijk and Veldhuijzen, 2010). More insights into DNIC have been gathered namely that it recruits cortical networks, which may explain why pain expectation, which relies on cortical structures, prevents DNIC (Goffaux et al., 2007). In line with this, a recent fMRI study performed in humans suggest that a lack of DNIC results from increased control of the DRt from the cortex (Youssef et al., 2016). Another interesting finding likely helping to comprehend DNIC modulation, is that DNIC involves the activation of opioid receptors at the DRt (de Resende et al., 2011). Interestingly, our work shows that opioids inhibit DRt descending facilitation, it is therefore likely that the expression of DNIC might also rely on a balance between descending inhibition and facilitation, with notably descending facilitation overpowering descending inhibition. Another evidence that pain facilitation likely opposes the effects of DNIC comes from a study showing that chronic treatment with morphine, which induces paradoxical opioid-induced hyperalgesia (Lee et al., 2011), was shown to eliminate DNIC by activating pain facilitatory neurons in the RVM (Okada-Ogawa et al., 2009). Additionally, several other recent studies show that descending spinal inhibitory noradrenergic pathways are necessary for the expression of DNIC (Bannister et al., 2015; Peters et al., 2015). Finally, DNIC is decreased in patients and animal models with chronic pain and studies using the rat show that pharmacologically increasing noradrenaline, which is deficient at the spinal cord during neuropathic pain (Hughes et al., 2013), as well as blocking serotoninergic descending facilitation mediated by 5-HT3 receptors, restores DNIC in neuropathic animals (Bannister et al., 2015). Taking these recent findings into account and given the fact that chronic pain results from an imbalance between descending inhibition and facilitation with the imbalance towards increasing descending facilitation (Ossipov et al., 2014), assessing DNIC in patients could potentially constitute a relevant tool to monitor alterations in the endogenous pain modulatory pathways (van Wijk and Veldhuijzen, 2010), which could potentially help identify patients at risk for development of chronic pain and ultimately help find better pain treatments.
Local Neurochemical Systems
Pain facilitation from the DRt is modulated by several neurotransmitters such as glutamate, opioid peptides, noradrenaline and GABA. The excitatory amino acid glutamate plays a key role in the pronociceptive actions of the DRt during the formalin test since the blockade of AMPA/KA, NMDA and mGlu1 glutamate receptors by the local administration of the respective antagonists significantly reduced formalin-induced pain behavior which was accompanied by a reduction of c-Fos expression at both the superficial and deep dorsal laminae (Ambriz-Tututi et al., 2013). The tonic activity of glutamate at the DRt likely results from the sustained peripheral afferent input, induced by formalin injection, leading to increased activation of spino-DRt-spinal reverberative circuits (Almeida et al., 1993, 2000). Noradrenaline is also involved in the mediation of pronociception from the DRt. Indeed, noradrenaline release at the DRt, measured by in vivo microdialysis, increases during the formalin test (Martins et al., 2013). The reduction of noradrenaline release at the DRt by genetic manipulation of DRt-noradrenergic afferents significantly attenuated pain behavior in the formalin test while increasing local extracellular levels of noradrenaline, by inhibiting its recapture, produced the opposite effect (Martins et al., 2013). The genetic manipulation of DRt-noradrenergic afferents was performed by a viral vector derived from the Herpes Simplex virus type 1 (HSV-1) which is retrogradely transported from the DRt to its noradrenergic afferents, namely the locus coeruleus (LC) and A5 noradrenergic cell group (Figure 2), where it selectively reduces noradrenaline synthesis (Martins et al., 2010). The pain facilitatory actions of noradrenaline at the DRt are mediated through activation of α1-adrenoreceptors (Martins et al., 2013).
Opioid peptides were shown to inhibit DRt pain facilitation as shown by HSV-1-mediated overexpression of enkephalin at the DRt, which produced anti-hyperalgesia in a model of acute pain (Martins et al., 2008). Opioids likely act through direct inhibition of DRt spinally projecting neurons since these neurons express μ-opioid receptors (Pinto et al., 2008a,b). Opioids also act the DRt through additional inhibitory mechanisms, likely by disinhibiting enkephalinergic interneurons which receive input from GABAergic interneurons expressing μ-opioid receptors and being presynaptically inhibited by δ-opioid expressing-fibers (Pinto et al., 2008a). Opioid peptides responsible for the anti-hyperalgesic action found in our studies are mostly released from local interneurons but also from DRt afferent sources namely the RVM, the A5 noradrenergic cell group and the hypothalamus (Figure 2; Martins et al., 2008).
The inhibitory neurotransmitter GABA is involved in the mediation of pronociception from the DRt. Our recent studies show that GABA release at the DRt, measured by in vivo microdialysis, increases during the formalin test and that it increases DRt pain facilitation through activation of GABAB receptors (Martins et al., 2015a). Indeed, GABAB receptors knock-down at the DRt, mediated by lentiviral vectors, or the pharmacological blockade, via the local administration of a GABAB antagonist, significantly attenuated formalin-induced pain behavior while the local administration of a GABAB agonist induced the opposite (Martins et al., 2015a). The effect of GABA is likely due to disinhibition of the DRt spinally projecting neurons since a large proportion of GABAB receptors are expressed by local opioidergic neurons inhibiting DRt spinally projecting neurons (Pinto et al., 2007, 2008a; Martins et al., 2008). GABA might be released from local interneurons but also from insular, somatosensory and motor cortices (Figure 2) which represent the most important afferent pathways to the DRt and they are GABAergic (Martins et al., 2015a).
The RVM-VLM-DRt Triad as a Key Gateway for Top-Down Pain Modulation
The three components of the triad of RF medullary addressed in this review (RVM, VLM and DRt) are interconnected (Figure 1). The VLM↔DRt reciprocal connection is likely to have functional implications since the magnitude of nociceptive neuronal activation in two regions in response to nociceptive stimulation is positively correlated (Pinto et al., 2006). Similar correlation studies should be enlarged to the RVM.
The RVM-VLM-DRt triad is in a privileged position to collect input from higher brain centers and convey this modulation to the spinal cord (Figure 1). The RVM conveys input from the PAG which, on its turn, is an area that integrates modulatory influences arising from the areas involved in cognitive and emotional aspects of the pain response, such as the frontal cortex and the amygdala (Tracey and Mantyh, 2007). Furthermore, the RVM-VLM-DRt triad has the unique feature of being involved in bidirectional pain modulation, namely by balancing pain inhibition and pain facilitation (Figure 1). The triad is acted by the main relevant neurotransmitters involved in pain modulation, namely opioids, noradrenaline and serotonin, which has a putative translational value since most pain killers act at the opioidergic and monoaminergic systems. We therefore propose that the triad RVM-VLM-DRt is a key gateway in top-down directional pain modulation (Figure 1).
Due to our expertise in the study of the DRt and its peculiar role in pain facilitation, this part of the triad should be analyzed in detail. The DRt is a major integrative relay for ascending nociceptive information participating in a reticulo-thalamo-cortical pathway (Figure 2) through which the DRt may allow any signal of pain to again access to widespread areas of the neocortex and thus help prime the cortex for attentional reactions and/or the coordination of motor responses (Bernard et al., 1990; Villanueva et al., 1998; Monconduit et al., 1999, 2002; Desbois and Villanueva, 2001). The DRt receives projections from several brain areas predominantly from several cortical areas, the hypothalamus, the amygdala and brainstem areas involved in descending pain modulation (Figure 2). Besides the RVM and VLM, the DRt receives projections from the PAG, and a strong noradrenergic input from the pontine noradrenergic cell groups LC, A5 and A7 (Almeida et al., 2002).
The DRt is also a major integrative relay for descending nociceptive modulation from several brain areas including the cortex (Zhang et al., 2005), the hypothalamus (Amorim et al., 2015) and the brainstem (Martins et al., 2013; Velo et al., 2013; Leiras et al., 2016). The DRt was shown to relay descending pain facilitation from the anterior cingulate cortex (ACC; Zhang et al., 2005). Additionally, the DRt receives dense innervation from cortical areas, namely from the motor (M1 and M2), somatosensory (S1 and S2) and insular cortex (Desbois et al., 1999; Almeida et al., 2002). Our recent work demonstrated that a high percentage of the cortical projections to the DRt were GABAergic (Figure 2) and the release of GABA at the DRt enhanced DRt pain facilitation (Martins et al., 2015a). Therefore, it is likely that the DRt might relay descending facilitatory actions triggered from these cortical areas. Moreover, given the involvement of some of this cortical areas in the emotional and cognitive control, the GABAergic projections from these areas may represent a neuronal circuit that accounts for pain enhancement during imbalance of emotional and cognitive conditions. The DRt also relays descending nociceptive facilitation induced by galanin in the dorsomedial nucleus of the hypothalamus (Amorim et al., 2015). Our recent functional studies show that the DRt acts as an important relay station in the mediation of descending facilitation from noradrenergic areas, namely the LC and A5 noradrenergic groups (Martins et al., 2013). The LC exerts a bidirectional role on pain modulation (Hickey et al., 2014) and its pain facilitatory role is relayed by the DRt (Martins et al., 2010, 2013, 2015b).
The DRt is also involved in a network of reciprocal connections established between collaterals of DRt and medial medullary reticular spinally-projecting neurons (Figure 2; Leiras et al., 2016). Medial medullary reticular neurons are involved in nociceptive and escape motor responses (Casey and Morrow, 1989), it is therefore likely that the DRt might integrate noxious sensing and nocifensive behavior through the collaterals of descending axons with medullary reticulospinal neurons.
The extensive ascending and descending connections of the RVM-VLM-DRt triad allow it to modulate the spinal nociceptive signals and integrate those signals with environmental and emotional conditions providing adequate and adaptable pain responses while preserving the homeostasis of the organism. Based on the phylogenetically conserved nature of the RF, we propose that the RVM-VLM-DRt triad is a conserved part of the brain and represents a vital gateway which evaluates and controls pain responses and triggers adequate and integrated responses. In a very recent review, a role for the brainstem RF in emotional control has been discussed in detail (Venkatraman et al., 2017). The brainstem has been proposed the key region to provide the effective link between sensory and effectors networks in processing emotions. By harboring components of the emotional motor system, the RVM-VLM-DRt triad can provide both the rapid “fight or flight” responses necessary to provide a rapid and specific body reaction but also the responses adequate to process “slow burning” somatic and visceral pain signals (Parvizi and Damasio, 2001; Craig, 2003). Based on the intrinsic interconnections of the RVM-VLM-DRt triad, it may also represent, by excellence, an example of the structural connectome of the central homeostatic network (Edlow et al., 2016), namely in its involvement in pain responses. Pain is a main challenger of the body homeostasis, both in acute pain when cardiovascular and motor reactions should be rapidly adjusted, and in chronic pain, when anxiety, depression and even neurodegeneration can occur.
Chronic Pain as a Trigger of Neuroplasticity at the RVM-VLM-DRt Triad
The data gathered in several animal models point to a participation of the RVM-VLM-DRt triad in chronic pain. It remains to be ascertained if that RF triad plays a similar role in the human brain but the still low resolution of imaging techniques does not allow detailed studies of those medullary regions. The interesting perspectives derived from recent imaging studies (Brooks et al., 2017) is likely to provide important data in a near future.
During chronic inflammatory pain several studies indicate that the activity of the triad is altered. Increased activity at the VLM and DRt were detected in a functional study based in the consumption of 2-D-glucose in chronic monoarthitic rats (Neto et al., 1999). In the specific case of the DRt, this could be related both to increased spinal excitatory inputs to the DRt in addition to a loss of inhibitory opioidergic tone into the DRt. The former was suggested to occur due to an imbalance between excitatory and inhibitory actions exerted upon spino-DRt neurons. Spinal dorsal horn neurons projecting to the DRt are under direct inhibitory GABAergic modulation, as they express mainly GABAB receptors (Castro et al., 2006) but in the spinal dorsal horn of monoarthritic animals there are lower percentages of GABAB expressing neurons and higher percentages of NK1 neurons (Castro et al., 2005) which are being subjected to excitatory actions exerted by substance P. A loss of inhibitory opioidergic tone likely occurs at the DRt since monoarthritic rats show decreased expression levels of of μ- and δ-opioid receptors at the DRt (Neto et al., 2008; Pinto et al., 2008a). These hypotheses are consistent with the results of a recent study showing the involvement of the DRt in formalin-induced secondary allodynia and hyperalgesia through a tonic glutamatergic excitatory tone (Ambriz-Tututi et al., 2013). Indeed, the administration of glutamate antagonists into the DRt reduced both secondary allodynia and hyperalgesia and their development was prevented by pretreatment with glutamate antagonists injected into the DRt before formalin injection (Ambriz-Tututi et al., 2013). The results of this study further support a key role for glutamate receptors into the DRt in the development of formalin-induced secondary allodynia and hyperalgesia.
Neuropathic pain is associated with spinal neuronal sensitization (Laird and Bennett, 1993), an activity-dependent expression of hypersensitivity of spinal neurons. Electrophysiological studies suggest a contribution of the DRt to the maintenance of spinal sensitization during neuropathic pain (Sotgiu et al., 2008). The recent studies performed by our group implicate the noradrenergic modulation of the DRt in the enhancement of DRt pain facilitation during neuropathic pain. We showed that nociceptive stimulation increased noradrenaline release at the DRt which enhanced pain facilitation from the DRt through activation of α1-adrenoreceptors (Martins et al., 2015b). Reducing noradrenaline release at the DRt by using a viral vector derived from the HSV-1 which selectively reduced noradrenaline synthesis in noradrenergic DRt afferents, significantly attenuated the behavioral manifestations of neuropathic pain for nearly 2 months (Martins et al., 2010). Our studies also show an impairment of the feedback inhibitory function of α2-adrenoreceptors at the DRt during neuropathic pain, which likely further contributes to enhance the noradrenergic input to the DRt during neuropathic pain (Martins et al., 2015b). The increased noradrenergic neurotransmission at the DRt, enhancing pain facilitation from this area, raises an important issue related to the treatment of neuropathic pain with antidepressants inhibiting noradrenaline reuptake. Noradrenaline reuptake inhibitors are known to produce analgesia through a spinal action but our results also show that they may enhance pain facilitation from the brain counteracting thus their analgesic effects at the spinal cord.
The occurrence of irreversible changes during the installation of chronic pain should also be considered since it was demonstrated that the RVM suffers neurodegeneration during the installation of neuropathy. In initial phases of neuropathy, the RVM exhibits plastic changes in what concerns its involvement in descending modulation namely by increases in the activity of pain facilitatory ON-neurons and opposite for OFF-neurons, along with an enhancement of pain facilitatory actions at the spinal cord mediated by local 5-HT3 receptors (Silva et al., 2013, 2016a; Guo et al., 2014). Collectively these changes lead to increase in descending pain facilitation which may account for chronic pain installation. During the progression of pain, and due to the continuous barrage of nociceptive input from the spinal cord, a disruption of local RVM circuits occurs with the appearance of massive oxidative stress damage and hyperactivation of glial cells (Silva et al., 2016a). The subsequent neuroinflammation may lead to neurodegeneration, associated with neuronal loss, which represents a non-plastic effect of chronic pain installation at the RVM. Neuroplastic changes in key descending pain modulatory areas were shown to be crucial for the generation and maintenance of chronic pain (Woolf and Salter, 2000), the studies compiled here strongly suggest that the alterations occurring at the RVM-VLM-DRt triad during chronic pain are also fundamental to its maintenance. Additionally, our results highlight the necessity of taking into account the alterations occurring at the levels of the RF for the design of efficient therapies for the challenging treatment of chronic pain.
Future Directions in the Study of the Reticular Formation
Functional neuroanatomical studies rely on the coupling of neural tracing with other neuroscientific techniques such as electrophysiology and behavior. In the last few years these studies have been massively propelled by the use of novel technologies such as optogenetics and chemogenetics which allow simultaneously manipulating circuitries and linking those circuits to behavioral outputs. Optogenetics use channels that are activated by light (Copits et al., 2016), while chemogenetics uses engineered G protein-coupled receptors, that are activated by otherwise inert drug-like small molecules, to activate or silence neuronal firing (Roth, 2016). Hitherto, optogenetics have been successfully used to study brain circuits such as those involved in regulation of the sensory and affective aspects of pain, namely cortico-limbic networks (Copits et al., 2016). Chemogenetics have also been successfully used to examine spinal circuits involved in pain modulation (Bourane et al., 2015; Peirs et al., 2015; Saloman et al., 2016) and the study of descending pain modulation is also starting to be approached by both technologies (Cai et al., 2014; Hickey et al., 2014; Jurik et al., 2015; Li et al., 2016). The RF contains areas relaying and integrating nociceptive information, from the brain and the spinal cord with other physiological functions. In the future the use of optogenetics and chemogenetics will allow a more comprehensive and precise study of the integrative role and the specificity of the intricate circuits of the RF.
At the clinical setting, the technical improvements at the brain imaging field will also allow to study the RF in more detail. By proposing that the medullary RF has a triad of pain control centers (the RVM-VLM-DRt), the technical problems of studying small components may be surpassed as the triad should be considered as a gateway from the brain to the spinal cord. The RVM-VLM-DRt triad probably represents an example of the “brain pain connectome” and should not be analyzed as to its individual components, per se. Future studies will analyze the RVM-VLM-DRt triad as a phylogenetically conserved structure of the RF which is vital in acute pain, namely to provide the substrate for “fight or flight responses”. Since the medullary triad is a gateway from descending modulation from the brain to the spinal cord, we should study in the future how the deregulation of the RVM-VLM-DRt triad in balancing inhibition and facilitation of pain may account for chronic pain generation and/or maintenance.
Author Contributions
IT was responsible for the overall organization of the manuscript and wrote the parts related to the rostroventromedial medulla and the ventrolateral medulla. IM was responsible for the items related to the role of the dorsal reticular nucleus. The overall manuscript was reviewed by both authors.
Funding
Supported by FPF7 EU Project REDDSTAR (FP7-Health-2012.2.4.3-1).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The reviewer ES and handling Editor declared their shared affiliation, and the handling Editor states that the process nevertheless met the standards of a fair and objective review.
Abbreviations
AT1, angiotensin type 1 receptors; DNIC, diffuse noxious inhibitory control; DRt, dorsal reticular nucleus; fMRI, functional magnetic resonance imaging; HSV-1, Herpes Simplex virus type 1; LC, locus coeruleus; LRt, lateral reticular nucleus; NRM, nucleus raphe-magnus; NTS, nucleus of the solitary tract; PAG, periaqueductal gray; RF, reticular formation; RVM, rostroventromedial medulla; Sp5C, spinal trigeminal nucleus; TRPV1, vanilloid receptor type 1; VLM, caudal ventrolateral medulla; VLMlat, caudalmost part of the VLM; WDR, wide-dynamic range.
References
Almeida, A., Cobos, A., Tavares, I., and Lima, D. (2002). Brain afferents to the medullary dorsal reticular nucleus: a retrograde and anterograde tracing study in the rat. Eur. J. Neurosci. 16, 81–95. doi: 10.1046/j.1460-9568.2002.02058.x
Almeida, A., and Lima, D. (1997). Activation by cutaneous or visceral noxious stimulation of spinal neurons projecting to the medullary dorsal reticular nucleus in the rat: a c-fos study. Eur. J. Neurosci. 9, 686–695. doi: 10.1111/j.1460-9568.1997.tb01417.x
Almeida, T. F., Roizenblatt, S., and Tufik, S. (2004). Afferent pain pathways: a neuroanatomical review. Brain Res. 1000, 40–56. doi: 10.1016/j.brainres.2003.10.073
Almeida, A., Størkson, R., Lima, D., Hole, K., and Tjølsen, A. (1999). The medullary dorsal reticular nucleus facilitates pain behaviour induced by formalin in the rat. Eur. J. Neurosci. 11, 110–122. doi: 10.1046/j.1460-9568.1999.00411.x
Almeida, A., Tavares, I., and Lima, D. (1995). Projection sites of superficial or deep dorsal horn in the dorsal reticular nucleus. Neuroreport 6, 1245–1248. doi: 10.1097/00001756-199506090-00004
Almeida, A., Tavares, I., and Lima, D. (2000). Reciprocal connections between the medullary dorsal reticular nucleus and the spinal dorsal horn in the rat. Eur. J. Pain 4, 373–387. doi: 10.1053/eujp.2000.0193
Almeida, A., Tavares, I., Lima, D., and Coimbra, A. (1993). Descending projections from the medullary dorsal reticular nucleus make synaptic contacts with spinal cord lamina I cells projecting to that nucleus: an electron microscopic tracer study in the rat. Neuroscience 55, 1093–1106. doi: 10.1016/0306-4522(93)90323-8
Almeida, A., Tjølsen, A., Lima, D., Coimbra, A., and Hole, K. (1996). The medullary dorsal reticular nucleus facilitates acute nociception in the rat. Brain Res. Bull. 39, 7–15. doi: 10.1016/0361-9230(95)02027-6
Alstermark, B., and Ekerot, C. F. (2013). The lateral reticular nucleus: a precerebellar centre providing the cerebellum with overview and integration of motor functions at systems level. A new hypothesis. J. Physiol. 591, 5453–5458. doi: 10.1113/jphysiol.2013.256669
Ambriz-Tututi, M., Palomero-Rivero, M., Ramirez-López, F., Millán-Aldaco, D., and Drucker-Colín, A. R. (2013). Role of glutamate receptors in the dorsal reticular nucleus in formalin-induced secondary allodynia. Eur. J. Neurosci. 38, 3008–3017. doi: 10.1111/ejn.12302
Amorim, D., Viisanen, H., Wei, H., Almeida, A., Pertovaara, A., and Pinto-Ribeiro, F. (2015). Galanin-mediated behavioural hyperalgesia from the dorsomedial nucleus of the hypothalamus involves two independent descending pronociceptive pathways. PLoS One 10:e0142919. doi: 10.1371/journal.pone.0142919
Andrezik, J. A., and Beitz, A. J. (1985). “Reticular formation, central gray and related tegmental nuclei,” in The Rat Nervous System, ed. G. Paxinos (New York, NY: Academic Press), 1–28.
Bannister, K., Patel, R., Goncalves, L., Townson, L., and Dickenson, A. H. (2015). Diffuse noxious inhibitory controls and nerve injury: restoring an imbalance between descending monoamine inhibitions and facilitations. Pain 156, 1803–1811. doi: 10.1097/j.pain.0000000000000240
Bernard, J. F., Villanueva, L., Carroue, J., and Le Bars, D. (1990). Efferent projections from the subnucleus reticularis dorsalis (SRD): a Phaseolus vulgaris leucoagglutinin study in the rat. Neurosci. Lett. 116, 257–262. doi: 10.1016/0304-3940(90)90083-l
Bing, Z., Villanueva, L., and Le Bars, D. (1990). Ascending pathways in the spinal cord involved in the activation of subnucleus reticularis dorsalis neurons in the medulla of the rat. J. Neurophysiol. 63, 424–438.
Bouhassira, D., Bing, Z., and Le Bars, D. (1990). Studies of the brain structures involved in diffuse noxious inhibitory controls: the mesencephalon. J. Neurophysiol. 64, 1712–1723.
Bouhassira, D., Bing, Z., and Le Bars, D. (1992a). Effects of lesions of locus coeruleus/subcoeruleus on diffuse noxious inhibitory controls in the rat. Brain Res. 571, 140–144. doi: 10.1016/0006-8993(92)90520-j
Bouhassira, D., Villanueva, L., Bing, Z., and Le Bars, D. (1992b). Involvement of the subnucleus reticularis dorsalis in diffuse noxious inhibitory controls in the rat. Brain Res. 595, 353–357. doi: 10.1016/0006-8993(92)91071-l
Bouhassira, D., Chitour, D., Villanueva, L., and Le Bars, D. (1993). Morphine and diffuse noxious inhibitory controls in the rat: effects of lesions of the rostral ventromedial medulla. Eur. J. Pharmacol. 232, 207–215. doi: 10.1016/0014-2999(93)90775-d
Bourane, S., Duan, B., Koch, S. C., Dalet, A., Britz, O., Garcia-Campmany, L., et al. (2015). Gate control of mechanical itch by a subpopulation of spinal cord interneurons. Science 350, 550–554. doi: 10.1126/science.aac8653
Brooks, J. C., Davies, W. E., and Pickering, A. E. (2017). Resolving the brainstem contributions to attentional analgesia. J. Neurosci. 37, 2279–2291. doi: 10.1523/JNEUROSCI.2193-16.2016
Cahusac, P. M., and Hill, R. G. (1983). Alpha-2 adrenergic receptors on neurones in the region of the lateral reticular nucleus of the rat. Neurosci. Lett. 42, 279–284. doi: 10.1016/0304-3940(83)90275-6
Cai, Y. Q., Wang, W., Hou, Y. Y., and Pan, Z. Z. (2014). Optogenetic activation of brainstem serotonergic neurons induces persistent pain sensitization. Mol. Pain 10:70. doi: 10.1186/1744-8069-10-70
Carlson, J. D., Maire, J. J., Martenson, M. E., and Heinricher, M. M. (2007). Sensitization of pain-modulating neurons in the rostral ventromedial medulla after peripheral nerve injury. J. Neurosci. 27, 13222–13231. doi: 10.1523/JNEUROSCI.3715-07.2007
Casey, K. L., and Morrow, T. J. (1989). Effect of medial bulboreticular and raphe nuclear lesions on the excitation and modulation of supraspinal nocifensive behaviors in the cat. Brain Res. 501, 150–161. doi: 10.1016/0006-8993(89)91036-6
Castro, A. R., Morgado, C., Lima, D., and Tavares, I. (2006). Differential expression of NK1 and GABAB receptors in spinal neurones projecting to antinociceptive or pronociceptive medullary centres. Brain Res. Bull. 69, 266–275. doi: 10.1016/j.brainresbull.2005.12.004
Castro, A. R., Pinto, M., Lima, D., and Tavares, I. (2005). Imbalance between the expression of NK1 and GABAB receptors in nociceptive spinal neurons during secondary hyperalgesia: a c-Fos study in the monoarthritic rat. Neuroscience 132, 905–916. doi: 10.1016/j.neuroscience.2005.01.048
Copits, B. A., Pullen, M. Y., and Gereau, R. W. T. (2016). Spotlight on pain: optogenetic approaches for interrogating somatosensory circuits. Pain 157, 2424–2433. doi: 10.1097/j.pain.0000000000000620
Craig, A. D. (2003). A new view of pain as a homeostatic emotion. Trends Neurosci. 26, 303–307. doi: 10.1016/s0166-2236(03)00123-1
de Resende, M. A., Silva, L. F., Sato, K., Arendt-Nielsen, L., and Sluka, K. A. (2011). Blockade of opioid receptors in the medullary reticularis nucleus dorsalis, but not the rostral ventromedial medulla, prevents analgesia produced by diffuse noxious inhibitory control in rats with muscle inflammation. J. Pain 12, 687–697. doi: 10.1016/j.jpain.2010.12.009
Desbois, C., Le Bars, D., and Villanueva, L. (1999). Organization of cortical projections to the medullary subnucleus reticularis dorsalis: a retrograde and anterograde tracing study in the rat. J. Comp. Neurol. 410, 178–196. doi: 10.1002/(SICI)1096-9861(19990726)410:2<178::AID-CNE2>3.3.CO;2-6
Desbois, C., and Villanueva, L. (2001). The organization of lateral ventromedial thalamic connections in the rat: a link for the distribution of nociceptive signals to widespread cortical regions. Neuroscience 102, 885–898. doi: 10.1016/s0306-4522(00)00537-6
Dickenson, A. H., Le Bars, D., and Besson, J. M. (1980). Diffuse noxious inhibitory controls (DNIC). Effects on trigeminal nucleus caudalis neurones in the rat. Brain Res. 200, 293–305. doi: 10.1016/0006-8993(80)90921-x
Dugast, C., Almeida, A., and Lima, D. (2003). The medullary dorsal reticular nucleus enhances the responsiveness of spinal nociceptive neurons to peripheral stimulation in the rat. Eur. J. Neurosci. 18, 580–588. doi: 10.1046/j.1460-9568.2003.02782.x
Edlow, B. L., McNab, J. A., Witzel, T., and Kinney, H. C. (2016). The structural connectome of the human central homeostatic network. Brain Connect. 6, 187–200. doi: 10.1089/brain.2015.0378
Eippert, F., Bingel, U., Schoell, E. D., Yacubian, J., Klinger, R., Lorenz, J., et al. (2009). Activation of the opioidergic descending pain control system underlies placebo analgesia. Neuron 63, 533–543. doi: 10.1016/j.neuron.2009.07.014
Fairhurst, M., Wiech, K., Dunckley, P., and Tracey, I. (2007). Anticipatory brainstem activity predicts neural processing of pain in humans. Pain 128, 101–110. doi: 10.1016/j.pain.2006.09.001
Fields, H. L., Heinricher, M. M., and Mason, P. (1991). Neurotransmitters in nociceptive modulatory circuits. Annu. Rev. Neurosci. 14, 219–245. doi: 10.1146/annurev.neuro.14.1.219
Francois, A., Low, S. A., Sypek, E. I., Christensen, A. J., Sotoudeh, C., Beier, K. T., et al. (2017). A brainstem-spinal cord inhibitory circuit for mechanical pain modulation by GABA and enkephalins. Neuron 93, 822.e6–839.e6. doi: 10.1016/j.neuron.2017.01.008
Gebhart, G. F., and Ossipov, M. H. (1986). Characterization of inhibition of the spinal nociceptive tail-flick reflex in the rat from the medullary lateral reticular nucleus. J. Neurosci. 6, 701–713.
Goffaux, P., Redmond, W. J., Rainville, P., and Marchand, S. (2007). Descending analgesia—when the spine echoes what the brain expects. Pain 130, 137–143. doi: 10.1016/j.pain.2006.11.011
Gonçalves, L., Almeida, A., and Pertovaara, A. (2007). Pronociceptive changes in response properties of rostroventromedial medullary neurons in a rat model of peripheral neuropathy. Eur. J. Neurosci. 26, 2188–2195. doi: 10.1111/j.1460-9568.2007.05832.x
Guo, W., Miyoshi, K., Dubner, R., Gu, M., Li, M., Liu, J., et al. (2014). Spinal 5-HT3 receptors mediate descending facilitation and contribute to behavioral hypersensitivity via a reciprocal neuron-glial signaling cascade. Mol. Pain 10:35. doi: 10.1186/1744-8069-10-35
Heinricher, M. M. (2016). Pain modulation and the transition from acute to chronic pain. Adv. Exp. Med. Biol. 904, 105–115. doi: 10.1007/978-94-017-7537-3_8
Heinricher, M. M., and Fields, H. L. (2013). “Central nervous system mechanisms of pain modulation,” in Wall and Melzack’s Textbook of Pain, 6th Edn. eds S. B. McMahon, M. Koltzenburg, I. Tracey and D. Turk (Philadelphia, PA: Elsevier Saunders), 129–142.
Heinricher, M. M., Morgan, M. M., and Fields, H. L. (1992). Direct and indirect actions of morphine on medullary neurons that modulate nociception. Neuroscience 48, 533–543. doi: 10.1016/0306-4522(92)90400-v
Heinricher, M. M., Tavares, I., Leith, J. L., and Lumb, B. M. (2009). Descending control of nociception: specificity, recruitment and plasticity. Brain Res. Rev. 60, 214–225. doi: 10.1016/j.brainresrev.2008.12.009
Herrero, J. F., Laird, J. M., and López-García, J. A. (2000). Wind-up of spinal cord neurones and pain sensation: much ado about something? Prog. Neurobiol. 61, 169–203. doi: 10.1016/s0301-0082(99)00051-9
Hickey, L., Li, Y., Fyson, S. J., Watson, T. C., Perrins, R., Hewinson, J., et al. (2014). Optoactivation of locus ceruleus neurons evokes bidirectional changes in thermal nociception in rats. J. Neurosci. 34, 4148–4160. doi: 10.1523/JNEUROSCI.4835-13.2014
Hughes, S. W., Hickey, L., Hulse, R. P., Lumb, B. M., and Pickering, A. E. (2013). Endogenous analgesic action of the pontospinal noradrenergic system spatially restricts and temporally delays the progression of neuropathic pain following tibial nerve injury. Pain 154, 1680–1690. doi: 10.1016/j.pain.2013.05.010
Huma, Z., Ireland, K., and Maxwell, D. J. (2015). The spino-bulbar-cerebellar pathway: activation of neurons projecting to the lateral reticular nucleus in the rat in response to noxious mechanical stimuli. Neurosci. Lett. 591, 197–201. doi: 10.1016/j.neulet.2015.02.047
Hunt, S. P., Pini, A., and Evan, G. (1987). Induction of c-fos-like protein in spinal cord neurons following sensory stimulation. Nature 328, 632–634. doi: 10.1038/328632a0
Jurik, A., Auffenberg, E., Klein, S., Deussing, J. M., Schmid, R. M., Wotjak, C. T., et al. (2015). Roles of prefrontal cortex and paraventricular thalamus in affective and mechanical components of visceral nociception. Pain 156, 2479–2491. doi: 10.1097/j.pain.0000000000000318
Kucyi, A., and Davis, K. D. (2015). The dynamic pain connectome. Trends Neurosci. 38, 86–95. doi: 10.1016/j.tins.2014.11.006
Kucyi, A., and Davis, K. D. (2016). The neural code for pain: from single-cell electrophysiology to the dynamic pain connectome. Neuroscientist doi: 10.1177/1073858416667716 [Epub ahead of print].
Laird, J. M., and Bennett, G. J. (1993). An electrophysiological study of dorsal horn neurons in the spinal cord of rats with an experimental peripheral neuropathy. J. Neurophysiol. 69, 2072–2085.
Le Bars, D. (2002). The whole body receptive field of dorsal horn multireceptive neurones. Brain Res. Rev. 40, 29–44. doi: 10.1016/s0165-0173(02)00186-8
Le Bars, D., Dickenson, A. H., and Besson, J. M. (1979). Diffuse noxious inhibitory controls (DNIC). I. Effects on dorsal horn convergent neurones in the rat. Pain 6, 283–304. doi: 10.1016/0304-3959(79)90049-6
Lee, M., Silverman, S. M., Hansen, H., Patel, V. B., and Manchikanti, L. (2011). A comprehensive review of opioid-induced hyperalgesia. Pain Physician 14, 145–161.
Leiras, R., Martin-Cora, F., Velo, P., Liste, T., and Canedo, A. (2016). Cat’s medullary reticulospinal and subnucleus reticularis dorsalis noxious neurons form a coupled neural circuit through collaterals of descending axons. J. Neurophysiol. 115, 324–344. doi: 10.1152/jn.00603.2015
Li, Y., Hickey, L., Perrins, R., Werlen, E., Patel, A. A., Hirschberg, S., et al. (2016). Retrograde optogenetic characterization of the pontospinal module of the locus coeruleus with a canine adenoviral vector. Brain Res. 1641, 274–290. doi: 10.1016/j.brainres.2016.02.023
Lima, D. (1990). A spinomedullary projection terminating in the dorsal reticular nucleus of the rat. Neuroscience 34, 577–589. doi: 10.1016/0306-4522(90)90166-2
Lima, D., Albino-Teixeira, A., and Tavares, I. (2002). The caudal medullary ventrolateral reticular formation in nociceptive-cardiovascular integration. An experimental study in the rat. Exp. Physiol. 87, 267–274. doi: 10.1113/eph8702354
Lima, D., and Almeida, A. (2002). The medullary dorsal reticular nucleus as a pronociceptive centre of the pain control system. Prog. Neurobiol. 66, 81–108. doi: 10.1016/s0301-0082(01)00025-9
Lima, D., and Coimbra, A. (1991). Neurons in the substantia gelatinosa rolandi (lamina II) project to the caudal ventrolateral reticular formation of the medulla oblongata in the rat. Neurosci. Lett. 132, 16–18. doi: 10.1016/0304-3940(91)90421-o
Lima, D., Mendes-Ribeiro, J. A., and Coimbra, A. (1991). The spino-latero-reticular system of the rat: projections from the superficial dorsal horn and structural characterization of marginal neurons involved. Neuroscience 45, 137–152. doi: 10.1016/0306-4522(91)90110-a
Lu, G. W., and Willis, W. D. (1999). Branching and/or collateral projections of spinal dorsal horn neurons. Brain Res. Rev. 29, 50–82. doi: 10.1016/s0165-0173(98)00048-4
Marques-Lopes, J., Pinho, D., Albino-Teixeira, A., and Tavares, I. (2010). The hyperalgesic effects induced by the injection of angiotensin II into the caudal ventrolateral medulla are mediated by the pontine A5 noradrenergic cell group. Brain Res. 1325, 41–52. doi: 10.1016/j.brainres.2010.02.043
Martins, I., Cabral, L., Pinto, A., Wilson, S. P., Lima, D., and Tavares, I. (2011). Reversal of inflammatory pain by HSV-1-mediated overexpression of enkephalin in the caudal ventrolateral medulla. Eur. J. Pain 15, 1008–1014. doi: 10.1016/j.ejpain.2011.04.007
Martins, I., Carvalho, P., de Vries, M. G., Teixeira-Pinto, A., Wilson, S. P., Westerink, B. H., et al. (2015a). GABA acting on GABAB receptors located in a medullary pain facilitatory area enhances nociceptive behaviors evoked by intraplantar formalin injection. Pain 156, 1555–1565. doi: 10.1097/j.pain.0000000000000203
Martins, I., Carvalho, P., de Vries, M. G., Teixeira-Pinto, A., Wilson, S. P., Westerink, B. H., et al. (2015b). Increased noradrenergic neurotransmission to a pain facilitatory area of the brain is implicated in facilitation of chronic pain. Anesthesiology 123, 642–653. doi: 10.1097/ALN.0000000000000749
Martins, I., Costa-Araujo, S., Fadel, J., Wilson, S. P., Lima, D., and Tavares, I. (2010). Reversal of neuropathic pain by HSV-1-mediated decrease of noradrenaline in a pain facilitatory area of the brain. Pain 151, 137–145. doi: 10.1016/j.pain.2010.06.027
Martins, I., de Vries, M. G., Teixeira-Pinto, A., Fadel, J., Wilson, S. P., Westerink, B. H., et al. (2013). Noradrenaline increases pain facilitation from the brain during inflammatory pain. Neuropharmacology 71, 299–307. doi: 10.1016/j.neuropharm.2013.04.007
Martins, I., Pinto, M., Wilson, S. P., Lima, D., and Tavares, I. (2008). Dynamic of migration of HSV-1 from a medullary pronociceptive centre: antinociception by overexpression of the preproenkephalin transgene. Eur. J. Neurosci. 28, 2075–2083. doi: 10.1111/j.1460-9568.2008.06492.x
McNaughton, N., and Corr, P. J. (2004). A two-dimensional neuropsychology of defense: fear/anxiety and defensive distance. Neurosci. Biobehav. Rev. 28, 285–305. doi: 10.1016/j.neubiorev.2004.03.005
Millan, M. J. (2002). Descending control of pain. Prog. Neurobiol. 66, 355–474. doi: 10.1016/S0301-0082(02)00009-6
Mobbs, D., Petrovic, P., Marchant, J. L., Hassabis, D., Weiskopf, N., Seymour, B., et al. (2007). When fear is near: threat imminence elicits prefrontal-periaqueductal gray shifts in humans. Science 317, 1079–1083. doi: 10.1126/science.1144298
Monconduit, L., Bourgeais, L., Bernard, J. F., Le Bars, D., and Villanueva, L. (1999). Ventromedial thalamic neurons convey nociceptive signals from the whole body surface to the dorsolateral neocortex. J. Neurosci. 19, 9063–9072.
Monconduit, L., Desbois, C., and Villanueva, L. (2002). The integrative role of the rat medullary subnucleus reticularis dorsalis in nociception. Eur. J. Neurosci. 16, 937–944. doi: 10.1046/j.1460-9568.2002.02148.x
Neto, F. L., Carvalhosa, A. R., Ferreira-Gomes, J., Reguenga, C., and Castro-Lopes, J. M. (2008). Delta opioid receptor mRNA expression is changed in the thalamus and brainstem of monoarthritic rats. J. Chem. Neuroanat. 36, 122–127. doi: 10.1016/j.jchemneu.2008.05.004
Neto, F. L., Schadrack, J., Ableitner, A., Castro-Lopes, J. M., Bartenstein, P., Zieglgänsberger, W., et al. (1999). Supraspinal metabolic activity changes in the rat during adjuvant monoarthritis. Neuroscience 94, 607–621. doi: 10.1016/s0306-4522(99)00185-2
Newman, D. B. (1985). Distinguishing rat brainstem reticulospinal nuclei by their neuronal morphology. I. Medullary nuclei. J. Hirnforsch. 26, 187–226.
Okada-Ogawa, A., Porreca, F., and Meng, I. D. (2009). Sustained morphine-induced sensitization and loss of diffuse noxious inhibitory controls in dura-sensitive medullary dorsal horn neurons. J. Neurosci. 29, 15828–15835. doi: 10.1523/JNEUROSCI.3623-09.2009
Ossipov, M. H. (2012). The perception and endogenous modulation of pain. Scientifica (Cairo) 2012:561761. doi: 10.6064/2012/561761
Ossipov, M. H., and Gebhart, G. F. (1986). Opioid, cholinergic and α-adrenergic influences on the modulation of nociception from the lateral reticular nucleus of the rat. Brain Res. 384, 282–293. doi: 10.1016/0006-8993(86)91164-9
Ossipov, M. H., Morimura, K., and Porreca, F. (2014). Descending pain modulation and chronification of pain. Curr. Opin. Support. Palliat. Care 8, 143–151. doi: 10.1097/SPC.0000000000000055
Palazzo, E., Luongo, L., Novellis, V., Rossi, F., and Maione, S. (2010). The role of cannabinoid receptors in the descending modulation of pain. Pharmaceuticals (Basel) 3, 2661–2673. doi: 10.3390/ph3082661
Panneton, W. M., Gan, Q., and Ariel, M. (2015). Injections of algesic solutions into muscle activate the lateral reticular formation: a nociceptive relay of the spinoreticulothalamic tract. PLoS One 10:e0130939. doi: 10.1371/journal.pone.0130939
Parvizi, J., and Damasio, A. (2001). Consciousness and the brainstem. Cognition 79, 135–160. doi: 10.1016/s0010-0277(00)00127-x
Peirs, C., Williams, S. P., Zhao, X., Walsh, C. E., Gedeon, J. Y., Cagle, N. E., et al. (2015). Dorsal horn circuits for persistent mechanical pain. Neuron 87, 797–812. doi: 10.1016/j.neuron.2015.07.029
Peters, C. M., Hayashida, K., Suto, T., Houle, T. T., Aschenbrenner, C. A., Martin, T. J., et al. (2015). Individual differences in acute pain-induced endogenous analgesia predict time to resolution of postoperative pain in the rat. Anesthesiology 122, 895–907. doi: 10.1097/ALN.0000000000000593
Pinto, M., Castro, A. R., Tshudy, F., Wilson, S. P., Lima, D., and Tavares, I. (2008a). Opioids modulate pain facilitation from the dorsal reticular nucleus. Mol. Cell. Neurosci. 39, 508–518. doi: 10.1016/j.mcn.2008.07.008
Pinto, M., Sousa, M., Lima, D., and Tavares, I. (2008b). Participation of μ-opioid, GABAB, and NK1 receptors of major pain control medullary areas in pathways targeting the rat spinal cord: implications for descending modulation of nociceptive transmission. J. Comp. Neurol. 510, 175–187. doi: 10.1002/cne.21793
Pinto, M., Lima, D., and Tavares, I. (2006). Correlation of noxious evoked c-fos expression in areas of the somatosensory system during chronic pain: involvement of spino-medullary and intra-medullary connections. Neurosci. Lett. 409, 100–105. doi: 10.1016/j.neulet.2006.08.031
Pinto, M., Lima, D., and Tavares, I. (2007). Neuronal activation at the spinal cord and medullary pain control centers after joint stimulation: a c-fos study in acute and chronic articular inflammation. Neuroscience 147, 1076–1089. doi: 10.1016/j.neuroscience.2007.05.019
Pinto-Ribeiro, F., Ansah, O. B., Almeida, A., and Pertovaara, A. (2011). Response properties of nociceptive neurons in the caudal ventrolateral medulla (CVLM) in monoarthritic and healthy control rats: modulation of responses by the paraventricular nucleus of the hypothalamus (PVN). Brain Res. Bull. 86, 82–90. doi: 10.1016/j.brainresbull.2011.06.014
Potrebic, S. B., Fields, H. L., and Mason, P. (1994). Serotonin immunoreactivity is contained in one physiological cell class in the rat rostral ventromedial medulla. J. Neurosci. 14, 1655–1665.
Rempe, T., Wolff, S., Riedel, C., Baron, R., Stroman, P. W., Jansen, O., et al. (2014). Spinal fMRI reveals decreased descending inhibition during secondary mechanical hyperalgesia. PLoS One 9:e112325. doi: 10.1371/journal.pone.0112325
Rempe, T., Wolff, S., Riedel, C., Baron, R., Stroman, P. W., Jansen, O., et al. (2015). Spinal and supraspinal processing of thermal stimuli: an fMRI study. J. Magn. Reson. Imaging 41, 1046–1055. doi: 10.1002/jmri.24627
Roth, B. L. (2016). DREADDs for neuroscientists. Neuron 89, 683–694. doi: 10.1016/j.neuron.2016.01.040
Roy, J. C., Bing, Z., Villanueva, L., and Le Bars, D. (1992). Convergence of visceral and somatic inputs onto subnucleus reticularis dorsalis neurones in the rat medulla. J. Physiol. 458, 235–246. doi: 10.1113/jphysiol.1992.sp019415
Saloman, J. L., Scheff, N. N., Snyder, L. M., Ross, S. E., Davis, B. M., and Gold, M. S. (2016). Gi-DREADD expression in peripheral nerves produces ligand-dependent analgesia, as well as ligand-independent functional changes in sensory neurons. J. Neurosci. 36, 10769–10781. doi: 10.1523/JNEUROSCI.3480-15.2016
Silva, M., Amorim, D., Almeida, A., Tavares, I., Pinto-Ribeiro, F., and Morgado, C. (2013). Pronociceptive changes in the activity of rostroventromedial medulla (RVM) pain modulatory cells in the streptozotocin-diabetic rat. Brain Res. Bull. 96, 39–44. doi: 10.1016/j.brainresbull.2013.04.008
Silva, M., Costa-Pereira, J. T., Martins, D., and Tavares, I. (2016a). Pain modulation from the brain during diabetic neuropathy: uncovering the role of the rostroventromedial medulla. Neurobiol. Dis. 96, 346–356. doi: 10.1016/j.nbd.2016.10.002
Silva, M., Martins, D., Charrua, A., Piscitelli, F., Tavares, I., Morgado, C., et al. (2016b). Endovanilloid control of pain modulation by the rostroventromedial medulla in an animal model of diabetic neuropathy. Neuropharmacology 107, 49–57. doi: 10.1016/j.neuropharm.2016.03.007
Sotgiu, M. L., Valente, M., Storchi, R., Caramenti, G., and Mario Biella, G. E. (2008). Contribution by DRt descending facilitatory pathways to maintenance of spinal neuron sensitization in rats. Brain Res. 1188, 69–75. doi: 10.1016/j.brainres.2007.10.030
Soto, C., and Canedo, A. (2011). Intracellular recordings of subnucleus reticularis dorsalis neurones revealed novel electrophysiological properties and windup mechanisms. J. Physiol. 589, 4383–4401. doi: 10.1113/jphysiol.2011.212464
Soto, C., Martín-Cora, F. J., Leiras, R., Velo, P., and Canedo, A. (2008). Processing noxious information at the subnucleus reticularis dorsalis (SRD) of anesthetized cats: wind-up mechanisms. Pain 140, 190–208. doi: 10.1016/j.pain.2008.08.007
Sousa, M., Szucs, P., Lima, D., and Aguiar, P. (2014). The pronociceptive dorsal reticular nucleus contains mostly tonic neurons and shows a high prevalence of spontaneous activity in block preparation. J. Neurophysiol. 111, 1507–1518. doi: 10.1152/jn.00440.2013
Starowicz, K., Maione, S., Cristino, L., Palazzo, E., Marabese, I., Rossi, F., et al. (2007). Tonic endovanilloid facilitation of glutamate release in brainstem descending antinociceptive pathways. J. Neurosci. 27, 13739–13749. doi: 10.1523/JNEUROSCI.3258-07.2007
Tavares, I., Almeida, A., Albino-Teixeira, A., and Lima, D. (1997a). Lesions of the caudal ventrolateral medulla block the hypertension-induced inhibition of noxious-evoked c-fos expression in the rat spinal cord. Eur. J. Pain 1, 149–160. doi: 10.1016/s1090-3801(97)90073-2
Tavares, I., Lima, D., and Coimbra, A. (1997b). The pontine A5 noradrenergic cells which project to the spinal cord dorsal horn are reciprocally connected with the caudal ventrolateral medulla in the rat. Eur. J. Neurosci. 9, 2452–2461. doi: 10.1111/j.1460-9568.1997.tb01662.x
Tavares, I., and Lima, D. (1994). Descending projections from the caudal medulla oblongata to the superficial or deep dorsal horn of the rat spinal cord. Exp. Brain Res. 99, 455–463. doi: 10.1007/BF00228982
Tavares, I., and Lima, D. (2002). The caudal ventrolateral medulla as an important inhibitory modulator of pain transmission in the spinal cord. J. Pain 3, 337–346. doi: 10.1054/jpai.2002.127775
Tavares, I., and Lima, D. (2007). From neuroanatomy to gene therapy: searching for new ways to manipulate the supraspinal endogenous pain modulatory system. J. Anat. 211, 261–268. doi: 10.1111/j.1469-7580.2007.00759.x
Tavares, I., Lima, D., and Coimbra, A. (1993). Neurons in the superficial dorsal horn of the rat spinal cord projecting to the medullary ventrolateral reticular formation express c-fos after noxious stimulation of the skin. Brain Res. 623, 278–286. doi: 10.1016/0006-8993(93)91438-x
Tavares, I., Lima, D., and Coimbra, A. (1996). The ventrolateral medulla of the rat is connected with the spinal cord dorsal horn by an indirect descending pathway relayed in the A5 noradrenergic cell group. J. Comp. Neurol. 374, 84–95. doi: 10.1002/(sici)1096-9861(19961007)374:1<84::aid-cne6>3.0.co;2-j
Tracey, I., and Mantyh, P. W. (2007). The cerebral signature for pain perception and its modulation. Neuron 55, 377–391. doi: 10.1016/j.neuron.2007.07.012
Urban, M. O., and Gebhart, G. F. (1999). Central mechanisms in pain. Med. Clin. North Am. 83, 585–596. doi: 10.1016/S0025-7125(05)70125-5
van Wijk, G., and Veldhuijzen, D. S. (2010). Perspective on diffuse noxious inhibitory controls as a model of endogenous pain modulation in clinical pain syndromes. J. Pain 11, 408–419. doi: 10.1016/j.jpain.2009.10.009
VanderHorst, V. G., and Ulfhake, B. (2006). The organization of the brainstem and spinal cord of the mouse: relationships between monoaminergic, cholinergic and spinal projection systems. J. Chem. Neuroanat. 31, 2–36. doi: 10.1016/j.jchemneu.2005.08.003
Velo, P., Leiras, R., and Canedo, A. (2013). Electrophysiological study of supraspinal input and spinal output of cat’s subnucleus reticularis dorsalis (SRD) neurons. PLoS One 8:e60686. doi: 10.1371/journal.pone.0060686
Venkatraman, A., Edlow, B. L., and Immordino-Yang, M. H. (2017). The brainstem in emotion: a review. Front. Neuroanat. 11:15. doi: 10.3389/fnana.2017.00015
Villanueva, L., Bernard, J. F., and Le Bars, D. (1995). Distribution of spinal cord projections from the medullary subnucleus reticularis dorsalis and the adjacent cuneate nucleus: a Phaseolus vulgaris-leucoagglutinin study in the rat. J. Comp. Neurol. 352, 11–32. doi: 10.1002/cne.903520103
Villanueva, L., Bing, Z., Bouhassira, D., and Le Bars, D. (1989). Encoding of electrical, thermal and mechanical noxious stimuli by subnucleus reticularis dorsalis neurons in the rat medulla. J. Neurophysiol. 61, 391–402.
Villanueva, L., Bouhassira, D., Bing, Z., and Le Bars, D. (1988). Convergence of heterotopic nociceptive information onto subnucleus reticularis dorsalis neurons in the rat medulla. J. Neurophysiol. 60, 980–1009.
Villanueva, L., Cliffer, K. D., Sorkin, L. S., Le Bars, D., and Willis, W. D. Jr. (1990). Convergence of heterotopic nociceptive information onto neurons of caudal medullary reticular formation in monkey (Macaca fascicularis). J. Neurophysiol. 63, 1118–1127.
Villanueva, L., de Pommery, J., Menetrey, D., and Le Bars, D. (1991). Spinal afferent projections to subnucleus reticularis dorsalis in the rat. Neurosci. Lett. 134, 98–102. doi: 10.1016/0304-3940(91)90517-w
Villanueva, L., Desbois, C., Le Bars, D., and Bernard, J. F. (1998). Organization of diencephalic projections from the medullary subnucleus reticularis dorsalis and the adjacent cuneate nucleus: a retrograde and anterograde tracer study in the rat. J. Comp. Neurol. 390, 133–160. doi: 10.1002/(sici)1096-9861(19980105)390:1<133::aid-cne11>3.3.co;2-o
Villanueva, L., and Le Bars, D. (1995). The activation of bulbo-spinal controls by peripheral nociceptive inputs: diffuse noxious inhibitory controls. Biol. Res. 28, 113–125.
Willis, W. D., and Westlund, K. N. (1997). Neuroanatomy of the pain system and of the pathways that modulate pain. J. Clin. Neurophysiol. 14, 2–31. doi: 10.1097/00004691-199701000-00002
Woolf, C. J., and Salter, M. W. (2000). Neuronal plasticity: increasing the gain in pain. Science 288, 1765–1768. doi: 10.1126/science.288.5472.1765
Yarnitsky, D. (2010). Conditioned pain modulation (the diffuse noxious inhibitory control-like effect): its relevance for acute and chronic pain states. Curr. Opin. Anaesthesiol. 23, 611–615. doi: 10.1097/ACO.0b013e32833c348b
Youssef, A. M., Macefield, V. G., and Henderson, L. A. (2016). Cortical influences on brainstem circuitry responsible for conditioned pain modulation in humans. Hum. Brain Mapp. 37, 2630–2644. doi: 10.1002/hbm.23199
Keywords: serotonin, noradrenaline, analgesics, opioids, emotions, cognition, connectome
Citation: Martins I and Tavares I (2017) Reticular Formation and Pain: The Past and the Future. Front. Neuroanat. 11:51. doi: 10.3389/fnana.2017.00051
Received: 12 April 2017; Accepted: 19 June 2017;
Published: 05 July 2017.
Edited by:
Ugo Faraguna, University of Pisa, ItalyReviewed by:
Enrica Laura Santarcangelo, University of Pisa, ItalySusan Warren, University of Mississippi Medical Center School of Dentistry, United States
Copyright © 2017 Martins and Tavares. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Isaura Tavares, isatav@med.up.pt