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2.
Front Syst Neurosci ; 17: 1043664, 2023.
Article in English | MEDLINE | ID: mdl-36911226

ABSTRACT

Introduction: The ability to separate similar experiences into differentiated representations is proposed to be based on a computational process called pattern separation, and it is one of the key characteristics of episodic memory. Although pattern separation has been mainly studied in the dentate gyrus of the hippocampus, this cognitive function if thought to take place also in other regions of the brain. The perirhinal cortex is important for the acquisition and storage of object memories, and in particular for object memory differentiation. The present study was devoted to investigating the importance of the cellular mechanism of endocytosis for object memory differentiation in the perirhinal cortex and its association with brain-derived neurotrophic factor, which was previously shown to be critical for the pattern separation mechanism in this structure. Methods: We used a modified version of the object recognition memory task and intracerebral delivery of a peptide (Tat-P4) into the perirhinal cortex to block endocytosis. Results: We found that endocytosis is necessary for pattern separation in the perirhinal cortex. We also provide evidence from a molecular disconnection experiment that BDNF and endocytosis-related mechanisms interact for memory discrimination in both male and female rats. Discussion: Our experiments suggest that BDNF and endocytosis are essential for consolidation of separate object memories and a part of a time-restricted, protein synthesis-dependent mechanism of memory stabilization in Prh during storage of object representations.

3.
Neuropharmacology ; 181: 108338, 2020 12 15.
Article in English | MEDLINE | ID: mdl-33002500

ABSTRACT

Upon retrieval, an aversive memory can undergo destabilization and reconsolidation. A traumatic-like memory, however, may be resistant to this process. The present study sought to contribute with a strategy to overcome this potential issue by investigating whether generalized fear retrieval is susceptible to destabilization-reconsolidation that can be pharmacologically modified. We hypothesized that exposure to a context that elicits moderate generalization levels would allow a malleable memory state. We developed a fear conditioning protocol in context A (cxt-A) paired with yohimbine administration to promote significant fear to a non-conditioned context B (cxt-B) in rats, mimicking the enhanced noradrenergic activity reported after traumatic events in humans. Next, we attempted to impair the reconsolidation phase by administering clonidine (CLO) immediately after exposure to cxt-A, cxt-B, or a third context C (cxt-C) neither conditioned nor generalized. CLO administered post-cxt-B exposure for two consecutive days subsequently resulted in decreased freezing levels in cxt-A. CLO after cxt-B only once, after cxt-A or cxt-C in two consecutive days, or independently of cxt-B exposures did not affect fear in a later test. A 6-h-delay in CLO treatment post-cxt-B exposures produced no effects, and nimodipine administered pre-cxt-B exposures precluded the CLO action. We then quantified the Egr1/Zif268 protein expression following cxt-B exposures and CLO treatments. We found that these factors interact to modulate this memory destabilization-reconsolidation mechanism in the basolateral amygdala but not the dorsal CA1 hippocampus. Altogether, memory destabilization can accompany generalized fear expression; thus, we may exploit it to potentiate reconsolidation blockers' action.


Subject(s)
Fear/psychology , Generalization, Psychological , Memory Consolidation/physiology , Memory/physiology , Adrenergic alpha-Agonists/pharmacology , Animals , CA1 Region, Hippocampal/drug effects , Clonidine/pharmacology , Early Growth Response Protein 1/biosynthesis , Early Growth Response Protein 1/genetics , Extinction, Psychological , Male , Memory Disorders/chemically induced , Memory Disorders/psychology , Mental Recall , Rats , Rats, Wistar , Sympatholytics , Yohimbine
4.
Brain Struct Funct ; 224(9): 3117-3132, 2019 Dec.
Article in English | MEDLINE | ID: mdl-31511975

ABSTRACT

Exposure to stressful conditions induces long-lasting neurobiological changes in selected brain areas, which could be associated with the emergence of negative emotional responses. Moreover, the interaction of a stressful experience and the retrieval of an established fear memory trace enhance both fear expression and fear retention. Related to this, the stimulation of the dorsolateral part of the mesencephalic periaqueductal gray matter (dlPAG) prior to retrieval potentiates a fear memory trace previously acquired. Therefore, the question that arises is whether the dlPAG mediates the increased fear expression and fear retention after retrieval. Rats were subjected to a contextual fear conditioning paradigm using a single footshock, and 1 day later, rats were subjected to a stressful situation. As previously reported, there was an increase of freezing response only in those rodents that were re-exposed to the associated context at 1 and 5 days after stress exposure. Muscimol intra-dlPAG prior to the restraint event prevented such increase. Conversely, Muscimol intra-dlPAG infusion immediately after the stress experience had no effect on the resulting fear memory. When the neuroendocrine response to stress was explored, intra-dlPAG infusion of muscimol prior to stress decreased Fos expression in the paraventricular nucleus and serum corticosterone levels. Moreover, this treatment prevented the enhancement of the density of hippocampal "mature" spines associated with fear memory. In conclusion, the present results suggest that the dlPAG is a key neural site for the negative valence instruction necessary to modulate the promoting influence of stress on fear memory.


Subject(s)
Fear/physiology , Mental Recall/physiology , Periaqueductal Gray/physiology , Stress, Psychological/physiopathology , Animals , Conditioning, Classical , Dendritic Spines/physiology , Hippocampus/physiology , Male , Paraventricular Hypothalamic Nucleus/physiology , Rats, Wistar
5.
Neuroscience ; 406: 542-553, 2019 05 15.
Article in English | MEDLINE | ID: mdl-30935981

ABSTRACT

Upon retrieval, aversive associative memories may engage alternative processes depending on the conditioned stimulus exposure length. Generally, a short session maintains it through reconsolidation, and a long session inhibits it because of extinction learning. However, various experimental interventions have produced no memory changes when given after intermediate conditioned stimulus exposure events. The lack of effectiveness in the latter case has been explained by a stage of transition from reconsolidation to extinction, during which both phases are engaged but neither prevails. Alternatively, it would represent a novel, intermediate phase between reconsolidation and extinction. By combining a varying time of exposure to the paired context with the amnesic agent midazolam, and the introduction of a reinstatement procedure in the protocol to investigate the occurrence of extinction and/or reconsolidation, we aimed at addressing this question in female rats. Midazolam disrupted the reconsolidation of the original aversive memory and the consolidation of extinction memory when given after short (2 or 5 min, but not 1 min) and long (30 min) exposure to the paired context, respectively. There was reinstatement in the latter case only. Midazolam produced no memory changes when given after a session of 7 or 10 min, with reinstatement data suggesting the absence of reconsolidation in both cases. Noteworthy, drug effects on reconsolidation or extinction and the lack of action on the intermediate process were similar across the estrous cycle. Altogether, it was possible to check and dissociate three retrieval-dependent contextual fear memory processes using a more nuanced approach in females.


Subject(s)
Avoidance Learning/physiology , Estrous Cycle/physiology , Fear/physiology , Fear/psychology , Mental Recall/physiology , Animals , Female , Rats , Rats, Wistar
6.
Transl Psychiatry ; 9(1): 53, 2019 01 31.
Article in English | MEDLINE | ID: mdl-30705259

ABSTRACT

Fear memory overgeneralization contributes to the genesis and persistence of anxiety disorders and is a central hallmark in the pathophysiology of post-traumatic stress disorder (PTSD). Recent findings suggest that fear generalization is closely related to hippocampal dependency during retrieval. The selective serotonin reuptake inhibitor (SSRI) fluoxetine has been used as a first-line treatment for PTSD; however, how it exerts its therapeutic effect remains a matter of debate. Here, using contextual fear conditioning in rats, we show that chronic fluoxetine treatment prevents fear generalization and enhances subsequent extinction. Moreover, fluoxetine treatment after extinction prevents spontaneous recovery. The mechanism through which fluoxetine affects generalization and extinction seems to be through the postponement of systems consolidation, thereby maintaining hippocampal involvement during retrieval. Such an effect relies on a remodeling of dendritic spines in the hippocampus, as well as the number of mature, mushroom-type spines promoted by fluoxetine treatment. In order to further investigate whether fear generalization is a potential predictor of extinction effectiveness, we categorized a large naive population according to their generalization rate. We found that discriminator rats showed a better extinction profile compared to generalizers, suggesting that the generalization rate predicts extinction effectiveness. Hence, we propose that the therapeutic strategy of choice should take into account the extension of memory generalization, in which therapies based on extinction could induce a better outcome in patients who present less fear overgeneralization. These results open new avenues for the development of interventions that prevent fear generalization by maintaining memory dependency of the hippocampus.


Subject(s)
Dendritic Spines/drug effects , Fear/drug effects , Fluoxetine/administration & dosage , Hippocampus/drug effects , Learning/drug effects , Neuronal Plasticity/drug effects , Selective Serotonin Reuptake Inhibitors/administration & dosage , Animals , Conditioning, Classical , Dendritic Spines/physiology , Extinction, Psychological/drug effects , Extinction, Psychological/physiology , Fear/physiology , Generalization, Psychological/drug effects , Generalization, Psychological/physiology , Hippocampus/physiology , Learning/physiology , Male , Memory Consolidation/drug effects , Memory Consolidation/physiology , Rats, Wistar
7.
Neurobiol Learn Mem ; 155: 412-421, 2018 11.
Article in English | MEDLINE | ID: mdl-30195049

ABSTRACT

Fear extinction is defined as a decline in fear-conditioned responses following non-reinforced exposure to a fear conditioned stimulus, therefore the conditioned stimulus gains new predictive properties. Patients with anxiety related disorders (e.g.: PTSD) subjected to extinction-like exposure treatments often experience a relapse of symptoms. Stress is a risk factor for those psychiatric disorders and a critical modulator of fear learning that turns the memory resistant to the extinction process. Dendritic spines are the anatomical sites where neuronal activity reshapes brain networks during learning and memory processes. Thus, we planned to characterize the dynamics of synaptic remodeling before and after contextual fear extinction in the dorsal hippocampus (DH), and how this process is affected by a previous stress experience. Animals with or without previous stress were contextually fear conditioned and one day later trained in an extinction paradigm. Rats were sacrificed one day after conditioning (pre-extinction) or one day after extinction for spine density analysis in the DH. We confirmed that stress exposure induced a deficit in extinction learning. Further, a higher density of dendritic spines, particularly mature ones, was observed in the DH of non-stressed conditioned animals at pre-extinction. Interestingly, after extinction, the spine levels returned to the control values. Conversely, stressed animals did not show such spines boost (pre-extinction) or any other change (post-extinction). In contrast, such standard dynamics of dendritic changes as well as the behavioral extinction was recovered when stressed animals received an intra-basolateral amygdala infusion of midazolam prior to stress. Altogether, these findings suggest that stress hinders the normal dynamic of dendritic remodeling after fear extinction and this could be part of the neurobiological substrate that makes those memories resistant to be extinguished.


Subject(s)
Dendritic Spines/physiology , Extinction, Psychological/physiology , Fear/physiology , Hippocampus/physiology , Memory/physiology , Neuronal Plasticity , Stress, Psychological/psychology , Animals , Basolateral Nuclear Complex/physiology , Conditioning, Classical , Male , Mental Recall/physiology , Rats, Wistar
8.
Neuropharmacology ; 135: 253-267, 2018 06.
Article in English | MEDLINE | ID: mdl-29499274

ABSTRACT

The main κ opioid receptors (κORs) subtypes already described (κ1ORs and κ2ORs) are expressed in brain regions involved in aversive memory consolidation, including the dorsal hippocampus (DH). However, the role of DH κORs in consolidation of aversive memories with varied intensity and specificity is still uncertain. The present study aimed to investigate this question using pharmacological agents in rats subjected to a weak, moderate or strong contextual aversive conditioning (CAC) protocol. Antagonizing DH κORs with nor-binaltorphimine (nor-BNI), immediately after, but not 6 h later, a moderate CAC leads to intensified freezing behavior in the re-exposure to the paired context. Thus, indicating that DH κORs have an inhibitory role in the consolidation of an aversive memory. Increased DH κORs expression 1 h and 3 h after the moderate CAC was also observed. This up-regulation was absent in animals only exposed to the shock or to the context, indicating that this phenomenon requires a shock-context pairing to occur. Intra-DH nor-BNI infusion induced no changes following a weak CAC, but it was able to potentiate the expression of freezing behavior in novel and unpaired context after a strong CAC, indicating that DH κORs also modulate the consolidation of a more intense and generalized memory. Moreover, infusing the κ2ORs agonist GR 89696, but not the κ1ORs agonist U-69593, into the DH reduced the conditioned freezing expression. Nor-BNI pretreatment in a sub-effective dose prevented the κ2ORs agonist effects. Altogether, the present findings provide convergent evidence that κORs activation negatively modulates contextual aversive memory consolidation in rat dorsal hippocampus.


Subject(s)
Avoidance Learning/physiology , Hippocampus/metabolism , Memory Consolidation/physiology , Receptors, Opioid, kappa/metabolism , Analgesics, Opioid/pharmacology , Animals , Association , Avoidance Learning/drug effects , Benzeneacetamides/pharmacology , Conditioning, Psychological/drug effects , Conditioning, Psychological/physiology , Electroshock , Freezing Reaction, Cataleptic/drug effects , Freezing Reaction, Cataleptic/physiology , Hippocampus/drug effects , Male , Memory Consolidation/drug effects , Naltrexone/analogs & derivatives , Naltrexone/pharmacology , Narcotic Antagonists/pharmacology , Piperazines/pharmacology , Psychotropic Drugs/pharmacology , Pyrrolidines/pharmacology , Random Allocation , Rats, Wistar , Receptors, Opioid, kappa/agonists , Receptors, Opioid, kappa/antagonists & inhibitors
9.
Learn Mem ; 23(9): 465-78, 2016 09.
Article in English | MEDLINE | ID: mdl-27531837

ABSTRACT

It is known that a consolidated memory can return to a labile state and become transiently malleable following reactivation. This instability is followed by a restabilization phase termed reconsolidation. In this work, we explored whether an unrelated appetitive experience (voluntary consumption of diluted sucrose) can affect a contextual fear memory in rats during the reactivation-induced destabilization phase. Our findings show that exposure to an appetitive experience following reactivation can diminish fear retention. This effect persisted after 1 wk. Importantly, it was achieved only under conditions that induced fear memory destabilization. This result could not be explained as a potentiated extinction, because sucrose was unable to promote extinction. Since GluN2B-containing NMDA receptors in the basolateral amygdala complex (BLA) have been implicated in triggering fear memory destabilization, we decided to block pharmacologically these receptors to explore the neurobiological bases of the observed effect. Intra-BLA infusion with ifenprodil, a GluN2B-NMDA antagonist, prevented the fear reduction caused by the appetitive experience. In sum, these results suggest that the expression of a fear memory can be dampened by an unrelated appetitive experience, as long as memory destabilization is achieved during reactivation. Possible mechanisms behind this effect and its clinical implications are discussed.


Subject(s)
Appetitive Behavior , Basolateral Nuclear Complex/physiology , Fear , Memory Consolidation/physiology , Receptors, N-Methyl-D-Aspartate/physiology , Retention, Psychology/physiology , Animals , Excitatory Amino Acid Antagonists/administration & dosage , Male , Piperidines/administration & dosage , Rats, Wistar , Receptors, N-Methyl-D-Aspartate/antagonists & inhibitors
10.
Brain Struct Funct ; 221(4): 1861-75, 2016 05.
Article in English | MEDLINE | ID: mdl-25682264

ABSTRACT

The retrosplenial cortex (RSC) is one of the largest cortical areas in rodents, and is subdivided in two main regions, A29 and A30, according to their cytoarchitectural organization and connectivities. However, very little is known about the functional activity of each RSC subdivision during the execution of complex cognitive tasks. Here, we used a well-established fear learning protocol that induced long-lasting contextual fear memory and showed that during evocation of the fear memory, the expression of early growth response gene 1 was up-regulated in A30, and in other brain areas implicated in fear and spatial memory, however, was down-regulated in A29, including layers IV and V. To search for the participation of A29 on fear memory, we triggered selective degeneration of neurons within cortical layers IV and V of A29 by using a non-invasive protocol that takes advantage of the vulnerability that these neurons have MK801-toxicity and the modulation of this neurodegeneration by testosterone. Application of 5 mg/kg MK801 in intact males induced negligible neuronal degeneration of A29 neurons and had no impact on fear memory retrieval. However, in orchiectomized rats, 5 mg/kg MK801 induced overt degeneration of layers IV-V neurons of A29, significantly impairing fear memory recall. Degeneration of A29 neurons did not affect exploratory or anxiety-related behavior nor altered unconditioned freezing. Importantly, protecting A29 neurons from MK801-toxicity by testosterone preserved fear memory recall in orchiectomized rats. Thus, neurons within cortical layers IV-V of A29 are critically required for efficient retrieval of contextual fear memory.


Subject(s)
Fear/physiology , Gyrus Cinguli/physiology , Mental Recall/physiology , Neurons/physiology , Animals , Conditioning, Classical/drug effects , Conditioning, Classical/physiology , Dizocilpine Maleate/administration & dosage , Early Growth Response Protein 1/metabolism , Excitatory Amino Acid Antagonists/administration & dosage , Fear/drug effects , Gyrus Cinguli/drug effects , Male , Mental Recall/drug effects , Neurons/drug effects , Neurons/pathology , Rats , Rats, Wistar , Testosterone/administration & dosage
11.
Int J Neuropsychopharmacol ; 18(4)2015 Jan 23.
Article in English | MEDLINE | ID: mdl-25617327

ABSTRACT

BACKGROUND: Withdrawal from chronic ethanol facilitates the formation of contextual fear memory and delays the onset to extinction, with its retrieval promoting an increase in ethanol consumption. Consequently, manipulations aimed to reduce these aversive memories, may be beneficial in the treatment of alcohol discontinuation symptoms. Related to this, pharmacological memory reconsolidation blockade has received greater attention due to its therapeutic potential. METHODS: Here, we examined the effect of post-reactivation amnestic treatments such as Midazolam (MDZ, 3 mg/kg i.p) and Propranolol (PROP, 5 mg/kg i.p) on contextual fear memory reconsolidation in ethanol- withdrawn (ETOH) rats. Next, we examined whether the activation of N-methyl-D-aspartate (NMDA) receptors induced by d-cycloserine (DCS, 5 mg/kg i.p., a NMDA partial agonist) before memory reactivation can facilitate the disruptive effect of PROP and MDZ on fear memory in ETOH rats. RESULTS: We observed a resistance to the disruptive effect of both MDZ and PROP following memory reactivation. Although intra-basolateral amygdala (BLA; 1.25 ug/side) and systemic PROP administration attenuated fear memory in DCS pre-treated ETOH rats, DCS/MDZ treatment did not affect memory in these animals. Finally, a decrease of both total and surface protein expression of the α1 GABAA receptor (GABAA-R) subunit in BLA was found in the ETOH rats. CONCLUSIONS: Ethanol withdrawal facilitated the formation of fear memory resistant to labilization post-reactivation. DCS administration promoted the disruptive effect of PROP on memory reconsolidation in ETOH rats. The resistance to MDZ's disruptive effect on fear memory reconsolidation may be, at least in part, associated with changes in the GABAA-R composition induced by chronic ethanol administration/withdrawal.


Subject(s)
Anti-Anxiety Agents/pharmacology , Fear/drug effects , Memory/drug effects , Midazolam/pharmacology , Propranolol/pharmacology , Substance Withdrawal Syndrome/drug therapy , Amygdala/drug effects , Amygdala/physiopathology , Animals , Central Nervous System Depressants/pharmacology , Conditioning, Psychological/drug effects , Conditioning, Psychological/physiology , Cycloserine/pharmacology , Disease Models, Animal , Ethanol/pharmacology , Excitatory Amino Acid Agents/pharmacology , Fear/physiology , Male , Memory/physiology , Random Allocation , Rats, Wistar , Receptors, GABA-A/metabolism , Receptors, N-Methyl-D-Aspartate/agonists , Receptors, N-Methyl-D-Aspartate/metabolism , Substance Withdrawal Syndrome/physiopathology
12.
Hippocampus ; 25(5): 545-55, 2015 May.
Article in English | MEDLINE | ID: mdl-25600672

ABSTRACT

GABAergic signaling in the basolateral amygdala complex (BLA) plays a crucial role on the modulation of the stress influence on fear memory. Moreover, accumulating evidence suggests that the dorsal hippocampus (DH) is a downstream target of BLA neurons in contextual fear. Given that hippocampal structural plasticity is proposed to provide a substrate for the storage of long-term memories, the main aim of this study is to evaluate the modulation of GABA neurotransmission in the BLA on spine density in the DH following stress on contextual fear learning. The present findings show that prior stressful experience promoted contextual fear memory and enhanced spine density in the DH. Intra-BLA infusion of midazolam, a positive modulator of GABAa sites, prevented the facilitating influence of stress on both fear retention and hippocampal dendritic spine remodeling. Similarly to the stress-induced effects, the blockade of GABAa sites within the BLA ameliorated fear memory emergence and induced structural remodeling in the DH. These findings suggest that GABAergic transmission in BLA modulates the structural changes in DH associated to the influence of stress on fear memory.


Subject(s)
Basolateral Nuclear Complex/physiology , Dendritic Spines/physiology , Fear/physiology , Hippocampus/physiology , Memory/physiology , gamma-Aminobutyric Acid/metabolism , Animals , Basolateral Nuclear Complex/drug effects , Conditioning, Psychological/physiology , GABA Modulators/pharmacology , Male , Midazolam/pharmacology , Neuronal Plasticity/physiology , Random Allocation , Rats, Wistar , Restraint, Physical , Stress, Psychological/physiopathology , Synaptic Transmission/physiology
13.
Learn Mem ; 20(11): 611-6, 2013 Oct 15.
Article in English | MEDLINE | ID: mdl-24129097

ABSTRACT

The present research investigated the resulting contextual fear memory and structural plasticity changes in the dorsal hippocampus (DH) following stress and fear conditioning. This combination enhanced fear retention and increased the number of total and mature dendritic spines in DH. Intra-basolateral amygdala (BLA) infusion of midazolam prior to stress prevented both the enhancement of fear retention and an increase in the density of total and mature dendritic spines in DH. These findings emphasize the role of the stress-induced attenuation of GABAergic neurotransmission in BLA in the promoting influence of stress on fear memory and on synaptic remodeling in DH. In conclusion, the structural remodeling in DH accompanied the facilitated fear memory following a combination of fear conditioning and stressful stimulation.


Subject(s)
Amygdala/physiology , Dendritic Spines/physiology , Fear/physiology , Hippocampus/physiology , Memory/physiology , Neuronal Plasticity/physiology , Stress, Physiological , Amygdala/drug effects , Animals , Anti-Anxiety Agents/pharmacology , Conditioning, Classical , Midazolam/pharmacology , Rats , Rats, Wistar
14.
Learn Mem ; 20(5): 245-55, 2013 Apr 15.
Article in English | MEDLINE | ID: mdl-23589091

ABSTRACT

The present study investigates the fear memory resulting from the interaction of a stressful experience and the retrieval of an established fear memory trace. Such a combination enhanced both fear expression and fear retention in adult Wistar rats. Likewise, midazolam intra-basolateral amygdala (BLA) infusion prior to stress attenuated the enhancement of fear memory thus suggesting the involvement of a stress-induced reduction of the GABAergic transmission in BLA in the stress-induced enhancing effect. It has been suggested that, unlike the immediate-early gene Zif268 which is related to the reconsolidation process, the expression of hippocampal brain-derived neurotrophic factor (BDNF) is highly correlated with consolidation. We therefore evaluate the relative contribution of these two neurobiological processes to the fear memory resulting from the above-mentioned interaction. Intra-dorsal hippocampus (DH) infusions of either the antisense Zif268 or the inhibitor of the protein degradation (Clasto-Lactacystin ß-Lactone), suggested to be involved in the retrieval-dependent destabilization process, did not affect the resulting contextual memory. In contrast, the knockdown of hippocampal BDNF mitigated the stress-induced facilitating influence on fear retention. In addition, the retrieval experience elevated BDNF level in DH at 60 min after recall exclusively in stressed animals. These findings suggest the involvement of a hippocampal BDNF sensitive mechanism in the stress-promoting influence on the fear memory following retrieval.


Subject(s)
Amygdala/metabolism , Brain-Derived Neurotrophic Factor/metabolism , Fear/physiology , Hippocampus/metabolism , Memory/physiology , Stress, Psychological/metabolism , Amygdala/drug effects , Animals , Behavior, Animal/drug effects , Behavior, Animal/physiology , Early Growth Response Protein 1/antagonists & inhibitors , Fear/drug effects , GABA Modulators/pharmacology , Hippocampus/drug effects , Lactones/pharmacology , Male , Memory/drug effects , Midazolam/pharmacology , Oligodeoxyribonucleotides, Antisense/pharmacology , Rats , Rats, Wistar
15.
Neuropsychopharmacology ; 35(5): 1097-108, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20043007

ABSTRACT

It is well known that, under certain boundary conditions, the retrieval of a stable consolidated memory results into a labile one. During this unstable phase, memory can be vulnerable to interference by a number of pharmacological agents, including benzodiazepines. One of the goals of this study was to evaluate the vulnerability to midazolam (MDZ) after reactivation of recent and remote contextual fear memories in animals that experienced a stressful situation before learning. Animals were subjected to a restraint session and trained in a contextual fear paradigm the following day; consolidated memories were reactivated at different times after learning and different MDZ doses (1.5, 3.0 mg/kg) were administered to rats after reactivation. Our results show that MDZ did not affect memory reconsolidation in older-than-one-day memories of stressed animals, even after the administration of a higher MDZ dose and a longer reactivation session (5 min). In contrast, MDZ was effective in blocking reconsolidation at all memory ages in unstressed animals. In addition, the current research investigated whether activating NMDA sites before reactivation promotes the destabilization of resistant memories such as those of stressed animals. We tested the influence of pre-reactivation D-cycloserine (DCS), a partial NMDA agonist, on MDZ's effect on fear memory reconsolidation in stressed animals. Our findings indicate that DCS before reactivation promotes retrieval-induced lability in resistant memory traces, as MDZ-induced memory impairment in stressed rats became evident with pre-reactivation DCS but not after pre-reactivation sterile isotonic saline.


Subject(s)
Fear/drug effects , GABA Modulators/pharmacology , Memory/drug effects , Midazolam/pharmacology , Receptors, N-Methyl-D-Aspartate/metabolism , Stress, Psychological/physiopathology , Animals , Conditioning, Classical/drug effects , Conditioning, Classical/physiology , Cycloserine/pharmacology , Dose-Response Relationship, Drug , Fear/physiology , GABA Modulators/administration & dosage , Male , Memory/physiology , Midazolam/administration & dosage , Neurotransmitter Agents/pharmacology , Rats , Rats, Wistar , Receptors, N-Methyl-D-Aspartate/agonists , Time Factors
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