Extinction procedure induces pruning of dendritic spines in CA1 hippocampal field depending on strength of training in rats

Introduction

It has been reported that treatments that typically produce amnesia become innocuous when administered to animals that have been submitted to an enhanced learning experience. Thus, generalized interference with cholinergic or serotonergic central activity produces amnesia of inhibitory avoidance (IA) trained with relatively low levels of foot-shock, but memory remains intact when higher levels of stimulation are used during training (e.g., Duran-Arevalo et al., 1990; Galindo et al., 2008). Similarly, long-term memory deficits of IA are produced by hindrance of synaptic activity of the striatum, amygdala, and substantia nigra; in contrast, under this circumstance memory is spared after enhanced IA training (Giordano and Prado-Alcalá, 1986; Pérez-Ruíz and Prado-Alcalá, 1989; Parent et al., 1992, 1995; Parent and McGaugh, 1994; Prado-Alcalá, 1995; Cobos-Zapiaín et al., 1996; Salado-Castillo et al., 2011). Recently, it was found that enhanced IA training prevented the typical amnesic effects of cycloheximide, a protein synthesis inhibitor (Díaz-Trujillo et al., 2009). In spite of this evidence, the neurobiological mechanisms of the protective effect of enhanced learning against amnesic treatments remain completely unknown.

The hippocampus is also involved in memory consolidation of IA training, as shown by the deleterious effects of interference with hippocampal activity on retention of this task (Izquierdo et al., 1992; Ambrogi-Lorenzini et al., 1996; Stubley-Weatherly et al., 1996; Martínez et al., 2002), although enhanced learning of this task also protects against amnesia produced by reversible blockade of hippocampal activity (Quiroz et al., 2003).

One structural neuronal change that has been proposed as a substrate of long-term memory is related to changes in dendritic spine density (Horner, 1993; O'Malley et al., 2000; Leuner et al., 2003). There is also a growing body of evidence that strongly suggests that acquisition of novel information induces the development of dendritic spines in the hippocampus in a variety of learning tasks (Mahajan and Desiraju, 1988; Horner, 1993; Moser et al., 1994; Rusakov et al., 1997; O'Malley et al., 2000; Leuner et al., 2003; Restivo et al., 2009), including the one-trial step-through IA task used in the present study (O'Malley et al., 1998). In this case, hippocampal dentate spine density was increased 6 h after training and returned to basal levels at 72 h after training.

Not only is the hippocampus involved in acquisition of conditioned responses, but also in the process of extinction, i.e., in the learned diminution of the conditioned responses following withholding of the unconditioned or reinforcing stimuli (Szapiro et al., 2003; Vianna et al., 2003; Dillon et al., 2008). However, there is a conspicuous lack of information regarding spine formation in this type of learning, and still less regarding extinction of enhanced learning.

The aim of this work was to determine if extinction of an IA response that had been acquired with low, medium, and high (enhanced training) levels of foot-shock promotes spinogenesis in CA1 pyramidal neurons of the hippocampus. If such were the case, then it might represent a possible mechanism for the protective effect of enhanced learning on memory. We now report that IA induces changes in spine density in CA1 pyramidal neurons of the hippocampus which are dependent on the strength of training.

Materials and Methods

Animals

All experimental procedures were approved by the Animal Ethics Committee of Instituto de Neurobiología, Universidad Nacional Autónoma de México and were in compliance with the NIH Guidelines for the Care and Use of Laboratory Animals. The subjects were naive male Wistar rats (250–350 g), maintained in a room with a 12 h/12 h light-dark cycle (lights on at 7:00 h), housed individually in acrylic cages with food and tap water ad libitum.

Since the main goal of this work was to determine if extinction after enhanced training of IA induces changes in spine density in the hippocampus as compared to regular training, it was necessary to operationally define “enhanced training.” One way to establish such a definition was to test the effects of increasing foot-shock intensities upon resistance to extinction, which is a progressive decline in the magnitude of a conditioned response that is no longer reinforced. It is used as a measure of strength of learning, since resistance to extinction is stronger when the learning experience is also stronger. Therefore, in this experiment, independent groups of rats were given one of three different foot-shock intensities during training in order to find out whether in our experimental conditions a relatively high foot-shock intensity produces stronger resistance to extinction as compared with lower foot-shock intensities. There were 10 rats in each group. The brains of four animals of each group were used to analyze to the density of dendritic spines in the CA1 field of the hippocampus.

Apparatus

The apparatus is an alley with two distinct compartments of the same size (30 × 30 × 30 cm), separated by a guillotine door. The safe compartment had walls and lid of red-colored acrylic with a floor of stainless steel bars (6 mm in diameter, separated by 9 mm); it was illuminated by a 10W light bulb located in the center of its lid. The other non-illuminated compartment had front and back walls and floor made of stainless steel plates with its end walls and lid constructed of red-colored acrylic. The walls and floor were shaped as a trough, 20 cm wide at the top and 8 cm wide at the bottom. In the middle of the floor, a 1.5 cm slot separated the two stainless steel plates that make up the walls and floor. When in this compartment, the rats were in contact with both plates through which foot-shock was delivered. The apparatus was cleansed with 10% alcohol and rinsed with tap water before and after each rat occupied it. A square-pulse stimulator (Grass model No. S-48), in series with a constant current unit (Grass model No. CCU-1A) generated the foot-shock. Shock delivery and measurement of latencies to cross from one compartment to the other one were accomplished by use of automated equipment. The apparatus was located inside a dark, sound-proof room provided with background masking noise.

Handling

Before the behavioral experiments began each animal was handled by the experimenter. This consisted of gently touching and holding the rat with both hands using gloves for approximately 5 min for 3 consecutive days. All behavioral observations were carried out between 9:00 h and 13:00 h.

Training and extinction testing

On the day of training each animal was put inside the safe compartment; 10 s later the door dividing the two compartments was opened and the latency to cross to the other compartment was measured (training latency). When the animals crossed to this compartment the door was closed and a foot-shock (a train of 50 ms square pulses at 10 Hz) of 1.0, 2.0, or 3.0 mA was delivered. Five seconds later the door was reopened allowing the animal to escape to the safe compartment and the stimulator was turned off; this latency was also measured (escape latency). After 30 s in the safe compartment the animals were put back in their home cages. Starting 24 h after training, extinction of the task was measured on six consecutive days. To this end, the same procedure of training was followed except that the foot-shock was omitted; if the animal did not cross to the second compartment within 600 s a retention latency score of 600 was assigned and the session ended. After the last extinction session, four animals from each group were randomly selected to perform the histological analyses described below. Two control groups were added: one of them was subjected to the same training procedure, except that the foot-shock was not administered (0 mA group; n = 3). In the case of this group, once they had crossed to the darker compartment, the door was re-opened after 5 s, and if they did not return to the safe compartment within an additional 5 s, they were gently pushed back into it. Twenty-four hours later, and for six consecutive days, latency to enter the dark compartment was also measured. The animals of the second control group (n = 3) were kept under identical living conditions as those of the animals used for the behavioral study, but they never left the bioterium, except for sacrificing (Bio group).

Rapid Golgi Impregnation

Right after the sixth test of extinction the selected animals that had been trained, together with those of the 0 mA and Bio groups, were anesthetized with xylazine/ketamine and perfused transcardially with a buffered solution of 10% formalin (pH 7.4). After 24 h the brains were removed from the skull, and one 4 mm block containing the dorsal hippocampus (Bregma −2.8 to −4.2; Paxinos and Watson, 2005) was obtained from each animal. Each block of hippocampus was impregnated using the rapid Golgi technique, as modified by Diaz-Cintra et al. (1981). After 12 days, each block was transferred to a solution of 0.75% silver nitrate in double-distilled water for 12 h, washed in 50% alcohol, embedded in low-viscosity nitrocellulose, and cut along the frontal plane at a thickness of 120 μm. Each section was collected in 70% alcohol, dehydrated, and mounted in Entellan medium. Each slide had 16 sections of dorsal hippocampus and was assigned a random number to ensure that observers were blind to the experimental conditions.

Morphometric Analysis

Dendritic spine counts were performed on five complete, well-impregnated neurons of the CA1 dorsal hippocampus of each rat. This analysis was carried out with an Optiphot-2 Nikon microscope using a 100× objective (Plan-Apochromat, NA 0.8) and an optically calibrated reticule on the ocular 10× eyepiece. Photomicrographs were assembled from images obtained at different focal planes and reconstructed using Helicon Focus 5.1 software (LTD 2010).

The apical dendrites were divided into proximal, medial, and distal segments, where commissural, Schaffer collaterals, and perforant path fibers arrive, respectively (Amaral and Witter, 1989; Yeckel and Berger, 1990; Dudman et al., 2007). We counted the number of spines along a length of 25 μm of three secondary branches of each segment. Thus, three counts per segment were obtained from each neuron. We chose to analyze secondary branches, and not the main dendritic shaft, because the proximal segment of the main apical dendrite is devoid of spines within the first 100 μm from the soma (Megias et al., 2001; present inspection), and, obviously, no meaningful comparisons could have been made if the proximal segment of the main dendrite would have been taken into account. Dendritic spine density was calculated as the number of dendritic spines divided by the 25 μm of the dendritic branch that was analyzed.

Statistical Analyses

Because the measurement of retention was truncated at 600 s, nonparametric statistics were used in analyzing the behavioral results. Independent Kruskal–Wallis analyses of variance were computed for acquisition and escape latencies, and for retention latencies of each of the extinction sessions. When appropriate, the Mann–Whitney U-test was used to make comparisons between any two groups.

Independent One-Way ANOVAs were used to analyse spine density in each of the three segments of the apical dendrite. This was done because their different innervations (proximal, medial, and distal segments receive commissural, Schaffer collaterals and perforant path fibers, respectively) indicates that these segments are not homogenous neuronal elements but, rather, independent functional compartments. When the F-ratios were significant, Duncan's Multiple Range Test was used to determine potential statistical differences of pair-wise comparisons.

Results

Behavior

Training and escape latencies. The Kruskal–Wallis test revealed that there were no significant differences among the groups regarding training latencies (H(3) = 6.354, p = 0.096). Median training latencies of the 0.0, 1.0, 2.0, and 3.0 mA groups were: 13.0, 24.56, 18.13, and 23.1 s, respectively. Because the “escape” latency of the 0 mA group was not shock-motivated, in every rat this latency was higher than the median escape latency of the foot-shocked groups, as expected; for this reason only the 1.0, 2.0, and 3.0 mA groups were included in the Kruskal–Wallis analysis of escape latencies, which yielded non-significant differenced among them (H(2) = 0.467, p = 0.792). Escape latencies of the latter groups were: 1.8, 2.2, and 2.1 s, respectively.

Figure 1 depicts the retention of the IA behavior of each group during the 6 days of extinction. A very clear differential pattern of resistance to extinction was produced by the various foot-shock intensities used during training. The Kruskal–Wallis test revealed that there were highly significant differences among the groups on each of the six extinction sessions (p's < 0.001 for each session). As anticipated, the median latency scores of the 0 mA group were very low, always below 15 s, and they differed from those of the other groups in each session (p's ranging from 0.05 to 0.0001). At the other end, the 3.0 mA group displayed near perfect retention latencies on the first five extinction sessions, and a very high score on the sixth session, well above the other groups. Except for the first session, where its retention score did not differ from that of the 2.0 mA group, the 3.0 mA group had a significantly higher retention score than the other groups (p's ranging from 0.01 to 0.0001) across the six sessions. The score of the 2.0 mA group was significantly higher than that of the 1.0 mA group through the first five sessions (p's between 0.05 and 0.01), and in the sixth session, their performances were quite similar (p = 0.684).

FIGURE 1

Figure 1. Median retention latencies across the daily extinction sessions (EXT1–EXT6) displayed by the groups that had been trained in inhibitory avoidance with 1.0, 2.0, or 3.0 mA. Also shown is the step-through latency of the 0 mA (control) group. On every extinction session retention scores of each group differed significantly from the latency scores of the other groups, except for the two points within the open circles.

Histology

Figure 2 shows an example of a Golgi-stained pyramidal neuron, and magnified distal, middle and proximal segments where the number of spines was tallied along a length of 25 μm. The statistical analyses revealed that there were highly significant differences in spine density among the groups in the proximal (F_{(4, 266)} = 9.635, p = 0.0001), medial (F_{(4, 266)} = 26.978, p = 0.0001), and distal (F_{(4, 266)} = 20.245, p = 0.0001) segments. The Duncan's Multiple Range Test showed that there were no significant differences in spine density between the Bio and the 0 mA groups in any of the segments (Figure 3). Regarding the proximal segment, spine density of the Bio and the 0 mA groups was significantly higher than that of the 1.0, 2.0, and 3.0 mA groups; spine density was not significantly different among the latter three groups. In the medial segment, the Bio and the 0 mA groups also had a higher spine density than the 1.0, 2.0, and 3.0 mA groups; in turn, the 3.0 mA group showed a higher spine density than the 1.0 and 2.0 mA groups. Finally, in the distal segment, no significant differences among the Bio, 0 mA, and 3.0 mA groups were found; each of these groups differed significantly from the 1.0 and 2.0 mA groups.

FIGURE 2

Figure 2. Representative example of CA1 pyramidal cells stained with the rapid-Golgi technique (middle figure), and a camera lucida drawing of it (left figure). Insets on the right hand side show enlarged images of distal (D), medial (M), and proximal (P) segments of the apical dendrite. Dendritic spines could be easily seen in each image with examination at different focal planes. Scale bars: middle figure (20×) = 100 μm; insets (100×) = 25 μm.

FIGURE 3

Figure 3. Mean spine density values (spines per micrometer) in each of the three segments of the CA1 apical dendrite, found after six extinction sessions of animals trained in inhibitory avoidance with 0, 1.0, 2.0, or 3.0 mA, and of a control group that never left the bioterium, except for sacrificing (Bio). Solid lines over bars represent significant differences (p < 0.001) as compared to Bio and 0 mA groups; broken lines over bars represent significant differences (p < 0.001) as compared to the 3.0 mA group.

Percent change in spine density, relative to the Bio control group is depicted in Figure 4. It can be clearly seen the spine pruning in the three segments of the apical CA1 dendrite of all the trained groups, except that the high foot-shock group maintained normal spine density in the distal segment.

FIGURE 4

Figure 4. Effects of intensity of inhibitory avoidance training on percentage changes in spine density found after six extinction sessions, normalized to the BIO control group, in each of the three segments of the apical dendrites of neurons of the CA1 dorsal hippocampus of the rat.

Discussion

This is the first study, to our knowledge, to examine spine plasticity in the hippocampus after a procedure of extinction.

Two main results were obtained. First, as expected, the higher foot-shock intensity induced better learning, i. e., the 3.0 mA group showed significantly higher resistance to extinction, as it performed better than the other groups on the extinction sessions.

The second main finding was that extinction produced pruning of spines in the three segments of the apical dendrite in the groups that had been trained with the lower foot-shock intensities (1.0 and 2.0 mA). Just as interesting was the observation that animals submitted to an enhanced learning experience (3.0 mA group), which produced higher resistance to extinction, showed different spine densities along the length of the apical dendrite: there was pruning in the proximal segment, as was the case for the lower foot-shock groups, a significant increase in spine density in the medial segment, and a spine density that was as high as that of the control groups in the distal segment.

The reduction in spine numbers after extinction was not simply due to exposure to the experimental context nor to habituation to it; this inference can be made because such a reduction in spines was not observed in the group that was “trained” with 0 mA and exposed to the same context for the same number of sessions as the trained, foot-shocked groups.

The presumption that synaptic changes underlie memory storage is not new. On the first half of the twentieth century Pavlov (1927) and Konorski (1948) postulated that conditioning was a form of learning different from that engaged in extinction but that, nonetheless, these two learning processes were associated with the making of new synaptic connections. There is a good deal of experimental support for the notion that learning is associated to genesis of dendritic spines (Rusakov et al., 1997; O'Malley et al., 1998, 2000; Leuner et al., 2003; Marrone, 2007), but it is difficult to find reports dealing with spine dynamics and extinction.

Our results point to one probable mechanism of extinction and of the protective effect of enhanced learning against interference with long-term memory formation. It was quite clear that those groups that actually showed extinction (1.0 and 2.0 mA groups; Figure 1) also presented a significant degree of spine pruning along the three segments of the CA1 apical dendrites (Figure 3). In this case, the plastic change induced by extinction was in the form of a reduction of synaptic contacts in the apical dendrite, as can be implied by the reduction of spines, and suggests that extinction is linked to a decrement in excitatory inputs at the postsynaptic site. This finding goes counter to the hypotheses proposed by Pavlov (1927) and Konorski (1948), and clearly shows that the mechanisms underlying the new learned response (extinction) are quite different from that those mediating the original learning of the IA response, where spine density has been found to increase significantly (O'Malley et al., 1998).

On the other hand, the group that was trained with the highest foot-shock intensity (3.0 mA), showed perfect retention of the conditioned response through the first four sessions of extinction, and it was on the fifth session that this response only begun to decline. Thus, it is obvious that the behavior of this group reflected the effects of enhanced training. This heightened resistance to extinction was accompanied by a differential pattern of spine modifications through the length of the CA1 apical dendrite (Figure 4). Just as in the case of training with the lower foot-shock intensities, this group showed pruning in the proximal and medial segments of the apical dendrite. However, in the distal segment spine count was not different from the control groups. This interesting result may indicate that the maintenance of the conditioned response of this group, in spite of having been submitted to the process of extinction, may be due, at least in part, to the maintenance of synaptic connections mediated by these dendritic spines. The main afferent fibers of the distal segment of the apical dendrite, the perforant path, arise from the multimodal entorhinal cortex. It is tempting to speculate that this pathway conveys excitatory signals produced by the enhanced learning conditions, thus halting the natural pruning induced by the extinction of the conditioned response.

In a recent and stimulating article, Vetere et al. (2011) studied dendritic spine dynamics after long-term retention of contextual fear conditioning. A significant increase in the density and size of spines was found in the apical dendrites of the anterior cingulated and infralimbic cortices. Interestingly, after extinction of the conditioned response spine density returned to baseline but the proportion of large spines did not in the anterior cingulated cortex; the opposite outcome was seen in the infralimbic cortex. These authors concluded that fluctuations in spine density and spine shape occur in cortical regions during both the formation and the extinction of contextual fear memories. On the other hand, we found that extinction was accompanied by pruning of dendritic spines along the length of the apical dendrites of hippocampal CA1 cells of rats that had been trained in IA with relatively low foot-shocks, and no change in spine density in the distal dendrite when a high foot-shock was administered. These dissimilar findings show that extinction learning represents a complex phenomenon where different processes take place in different brain regions, which may be dependent upon the type of behavior that is being extinguished.

It is worth mentioning that one distinctive feature of post-traumatic stress disorder (PTSD) is the formation of a strong memory that is highly resistant to extinction (Armario et al., 2008), akin to the memory formed after the enhanced learning of IA described in the present work. Thus, this behavioral model might be useful in the study of the neurobiology of PTSD, and one is tempted to hypothesize that resistance to extinction seen in this pathology could also be mediated by the durability of dendritic spines in the apical dendrites of the hippocampal pyramidal neurons.

To conclude, training of IA with a foot-shock of relatively high intensity (3.0 mA) produced enhanced learning, as shown by the strong resistance to extinction, as compared to the performance of the groups that had been trained with lower foot-shock intensities. After testing under a protocol to produce extinction, there was pruning of dendritic spines along the length of the apical dendrites in neurons of the CA1 field of the hippocampus in the animals that were trained with the lower foot-shock intensities (1.0 and 2.0 mA); these animals showed weak resistance to extinction. The group with the strong resistance to extinction also showed pruning of dendritic spines, but only in the proximal and medial segments of the apical dendrite; normal spine counts were found in the distal segment. Behavioral extinction, evidenced by the low retention scores, may be mediated, in part, by a plastic change in the form of a reduction of synaptic contacts in the apical dendrite, while maintenance of the conditioned response after the extinction protocol may be due, at least in part, to the maintenance of synaptic connections in the distal segment of the apical dendrite.

Further research is needed to put to the experimental test the various interpretations to the results offered in this work.

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.

Acknowledgments

We thank Ángel Méndez, Norma Serafín, Omar González, Martín García, and Ramón Martínez Olvera for their excellent technical assistance; and Dr. Dorothy Plerss for reviewing and helping us to improve the manuscript. Supported by the National Council of Science and Technology of México (Grant CONACYT 128259) and by PAPIIT-DGAPA-UNAM (Grant IN201712). This work was carried out in partial fulfillment of the requirements to obtain the Doctor's Degree (Doctorado en Ciencias Biomédicas, UNAM) by M. E. Garín-Aguilar, who was a recipient of a Graduate Scholarship from CONACYT (171434).

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