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Dendritic Spines in Depression: What We Learned from Animal Models

Hui Qiao, Ming-Xing Li, Chang Xu and 3 more

Neural Plasticity · 2016 · Review

doi:10.1155/2016/8056370

Abstract

Depression, a severe psychiatric disorder, has been studied for decades, but the underlying mechanisms still remain largely unknown. Depression is closely associated with alterations in dendritic spine morphology and spine density. Therefore, understanding dendritic spines is vital for uncovering the mechanisms underlying depression. Several chronic stress models, including chronic restraint stress (CRS), chronic unpredictable mild stress (CUMS), and chronic social defeat stress (CSDS), have been used to recapitulate depression-like behaviors in rodents and study the underlying mechanisms. In comparison with CRS, CUMS overcomes the stress habituation and has been widely used to model depression-like behaviors. CSDS is one of the most frequently used models for depression, but it is limited to the study of male mice. Generally, chronic stress causes dendritic atrophy and spine loss in the neurons of the hippocampus and prefrontal cortex. Meanwhile, neurons of the amygdala and nucleus accumbens exhibit an increase in spine density. These alterations induced by chronic stress are often accompanied by depression-like behaviors. However, the underlying mechanisms are poorly understood. This review summarizes our current understanding of the chronic stress-induced remodeling of dendritic spines in the hippocampus, prefrontal cortex, orbitofrontal cortex, amygdala, and nucleus accumbens and also discusses the putative underlying mechanisms.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 17, 2026. Paragraph numbers are ours, so an answer can point at one.

1. Introduction

Depression, a severe psychiatric disorder, affects up to 20% of the population in the US within their lifetime and is more prevalent in women than men. Although depression has been studied for decades, its cellular and molecular mechanisms still remain largely unknown. As many as 30–40% of patients with major depressive disorder have treatment-resistant depression which does not respond to currently available antidepressant therapies. It is therefore important to identify the mechanisms underlying depression in order to develop effective therapeutic strategies.

Chronic stress, especially psychosocial stressors in humans, is one well-known risk factor for the development of depression. Enhancement of neuronal plasticity is essential for adaptive intracellular changes during the normal stress response, which promotes dendritic growth, new synapse formation, and facilitates neuronal protein synthesis in the face of an acute challenge. In addition, a successful stress response requires continuity of the response to ensure normal brain function and promote survival. On the one hand, brief or moderate stressors actually enhance neural function in most cases, while severe or chronic stressors are detrimental and can disrupt the ability of the brain to maintain its normal stress response, eventually leading to depression. Furthermore, it has been shown that significant but brief stressful events (acute stress) result in the differentiation of stem cells into new nerve cells that improve the mental performance of rats. On the other hand, chronic stress increases the levels of the stress hormone glucocorticoid and suppresses the production of new neurons in the hippocampus. This response results in decreased dendritic spine density and synapse number and impaired memory. The relationship between stress and psychiatric diseases has been well established for 20 years in the clinic. Chronic stress paradigms in rodents, the classical animal model of depression, recapitulate many of the core behavioral features of depression and respond to antidepressant treatments. However, the precise nature of relationships among the effects of chronic stress, the dysregulation of spine/synapse plasticity, and the molecular mechanisms of depression remain poorly understood. This minireview summarizes our current understanding, obtained from animal models of chronic stress, of remodeling of dendritic spines in five regions of the brain during depression.

2. The Plasticity of Dendritic Spines

Dendritic spines are tiny membranous protrusions from the dendritic shaft of various types of neurons. They typically receive excitatory input from axons, although sometimes both inhibitory and excitatory connections are present on the same spine. Over 90% of all excitatory synapses that occur in the CNS are localized to dendritic spines, which are cellular substrates of brain connectivity and the major sites of information processing in the brain. Billions of neurons contact and communicate with each other via synapses. It is widely accepted that the regulation of dendritic spine number, size, and shape is of importance to the plasticity of synapses, as well as learning and memory. The morphology of spines is highly variable and commonly categorized into three types: thin, mushroom, and stubby (Figure 1). Large mushroom spines are memory spines carrying more biochemical signals and a number of human disease states are associated with alterations with spine morphology and/or spine density. Spines are thin if the length is greater than the neck diameter and the diameters of the head and neck are similar (Figure 1). Spines are classified as mushrooms if the diameter of the head is greater than the diameter of the neck. Spines are considered stubby if the length and width are equal. Spines are defined when they are no longer than three μm. The length of dendritic filopodia is normally >3 μm and <10 μm. The normal dendritic spine density ranges from 0.2 to 3.5 spines per 1 μm of dendrite depending on the neuron type, age, and position along the dendrite as well as the method of counting. Thin and stubby spines, as well as dendritic filopodia, are prevalent during development. Thin and stubby spines are considered to be immature, plastic spines. Dendritic filopodia are precursors of dendritic spines. The spine neck is an important structure for a mushroom spine to perform its normal function because the spine neck prevents Ca2+ exchange between the spine head and dendrite shaft. This is important for the regulation of synaptic transmission and may be neuroprotective, preventing excitotoxicity to the dendrite and neuron by restricting excessive influxes of Ca2+ within the synaptic region. Different spine types may serve different functions and changes in the ratio of these spines may have a greater effect on neuronal excitability and function. It is generally accepted that thin spines are learning spines, whereas large, mature, and less motile mushroom spines harboring larger and stronger synapses are memory spines that are responsible for the maintenance of neuronal networks and long-term memory. Large mushroom spines with large heads are stable and are likely to contain smooth endoplasmic reticulum, a spine apparatus, polyribosomes, and endosomal compartments in which posttranslational modification of proteins, local protein synthesis, local recycling of receptors, and membrane management occur, respectively. Large mushroom spines that contain abundant AMPA receptors are not restricted to pairing with presynaptic axonal terminals containing more synaptic vesicles. They can also associate with presynaptic astroglial terminals, which enhance synapse formation, stabilization, and synapse elimination. Mushroom spines with small heads are motile and unstable and contribute to weak or silent synaptic connections.

Dendritic spine pathology is associated with many psychiatric diseases. The formation, growth, and elimination of the dendritic spines are precisely controlled, which requires the reorganization of the neural network in response to acute stress or learning processes. These processes are commonly dysregulated or disrupted in chronically stressed animals. Therefore, understanding dendritic spines is fundamental in uncovering the mechanisms underlying depression. It is well established that depression is closely associated with selective structural changes, altered cellular resilience, and neuronal atrophy. Moreover, depression is associated with reduction in astrocytes and reduced/or increased volume of some brain regions that affect mood and cognition, which involve structural and molecular remodeling of dendritic spines in the hippocampus, prefrontal cortex, amygdala, and nucleus accumbens. Antidepressants have reversed some of these structural changes observed in animal models of depression. These studies have generated the hypothesis that alterations of the dendritic spines and the plasticity at excitatory synapses contribute to symptoms of depression.

3. Chronic Stress and Animal Models of Depression

Animal models are essential tools for studying and understanding specific symptoms of human psychiatric disorders, though none of the current models fully recapitulate stress-related psychiatric disorders described in humans. Most of the current knowledge about the mechanism underlying depression has come from animal models. Several animal models of depression have been used to understand the mechanisms underlying depression. We only discuss the model of chronic stress in this review. Several chronic stress models have been used to model depression-like behaviors in rodents such as chronic restraint stress (CRS), chronic unpredictable stress (CUS), and chronic social defeat stress (CSDS). Behavioral tests of anhedonia (sucrose preference) or despair (forced swim test and tail suspension test) have been widely used to determine depression-like behaviors induced by these three models. Depression-like behaviors induced by these models can often be reversed by chronic antidepressant treatments. It is, however, worth noting that there are some rats or mice that do not respond to traditional antidepressants, which is similar to treatment-resistant depression in human subjects. Here, we briefly summarize our current understanding about these three animal models.

3.1. Chronic Restraint Stress (CRS)

CRS has been used widely to study the morphological, hormonal, and behavioral alteration in several brain regions in rodents, such as the hippocampus, prefrontal cortex, amygdala, and nucleus accumbens because it is inexpensive and relatively easy to implement (Tables 1–4). To study dendritic morphology and spine formation, this method typically involves restraining an animal for 1–6 h each day in a restraint device (bag or tube) for a period of 14–21 days or more. A disadvantage of the CRS model is the habituation of rats or mice to repeated exposure to homotypic restraint stressors; the response of plasma corticosterone, the major glucocorticoids in rodents, to the final stressor is diminished in animals that had been stressed for 14 days. The pattern of hypothalamic corticotrophin-releasing hormone (CRH) heteronuclear RNA and mRNA responses to CRS is similar to the response of corticosterone, decreasing with increasing frequency of exposure to the repeated restraint stressor. Animals habituate over time and finally show no increase in hypothalamic-pituitary-adrenal (HPA) axis activation and no increase in expression of hypothalamic CRH. The duration of CRS may differentially affect learning/memory and CA3 dendritic atrophy with shorter periods of CRS (7–13 days) serving an adaptive function to enhance learning and memory. On the other hand, longer CRS duration (21 days or more) causes maladaptive changes such as dendrite atrophy, spine loss, and impaired memory. CRS-induced habitation of HPA axis contrasts with the hyperactivity of the HPA axis accompanied by increased CRH levels and the hypersecretion of cortisol in depressed patients, showing that activation of HPA axis is a hallmark of major depression. Depending on duration and intensity of chronic stress, some studies report that exposure of animals to CRS induces depression-like behaviors such as anhedonia (decreased sucrose preference), which is a core symptom of human depression. A conflicting report shows CRS could not induce anhedonic-like behavior. The duration and intensity of CRS as well as animal strains may determine whether CRS can be used as a valid animal model of depression to produce anhedonic-like behavior.

3.2. Chronic Unpredictable Mild Stress (CUMS)

CUMS is a well-established animal model for depression. The original, three-week chronic unpredictable severe stress (CUS) model with diverse severe and unpredictable stressors (electric shocks, immobilization, cold swimming, isolation housing, and other strong stimuli) was developed by Katz and coworkers. In order to accurately recapitulate the human condition, Willner and colleagues replaced severe stressors in Katz's model with mild stressors. Additionally, Willner and colleagues augmented the CUMS model with a variety of mild and unpredictable stressors (e.g., overnight illumination; presence of novel objects; periods of food and/or water deprivation; cage tilt; change of cage mate). In Willner's model, exposure of animals to 7–13 mild stressors up to 3 months produced a longer lasting depression-like behavior, anhedonia. The CUS model used in Duman's group was modified from Willner's model. In Duman's model, animals were exposed to 10 or 12 unpredictable stressors, 2 times per day, for up to 35 days, which produced depression-like behaviors. The duration of CUS is 21 days for the experiments using CUS alone or 35 days for the experiment using CUS together with antidepressant treatments. It is worth noting that CUS model used by Duman's group is different from the CUMS protocol, not only in the duration and number of stressors/day, but also at the level of stressor intensity (rotation on a shaker 1 hour, cold 4°C 1 hour, lights off for 3 hours, lights on overnight, strobe light overnight, aversive odor overnight, 45° tilted cages overnight, food and water deprivation overnight, crowded housing overnight, and isolation housing overnight). The modified CUMS model used in our laboratory consists of daily exposure of animals to 8 chronic unpredictable mild stressors, one stressor per day, for 21 days. The same stressor is not applied in two consecutive days. The different abbreviations of chronic unpredictable mild stress (CUS, CMS, or CUMS) were used in several modified versions by different laboratories. We use CUMS as a common denotation in this review. In comparison with the CRS model, CUMS overcomes stress habituation of the HPA axis occurring during stress, in which the response of plasma corticosterone to the final stressor is still sustained in animals which had been stressed for 15 to 35 days. Depression-like behaviors and deficits in synaptic plasticity are gradually developed during CUMS. The CUMS model recapitulates many of the core behavioral characteristics of human depression that are reversible by chronic treatments with traditional antidepressant agents and is more relevant to human disease. Therefore, the CUMS model has been widely used as an animal (specifically rat) model of depression. Our results show that, during CUMS, rats require three weeks to develop depression-like behaviors accompanied by both functional changes in CA3-CA1 synapses and decreased spine density in the dendrites of CA1 and CA3 pyramidal neurons. This is in line with Willner's CUMS paradigm, in which animals were exposed to initial unpredictable stress for three weeks to develop depression-like behaviors prior to the onset of antidepressant treatments. Because of its advantage of the gradual development of depression-like behaviors during CUMS, this model is useful in studying depression-like behaviors such as anhedonia. In addition, this CUMS model is useful for inducing depression-like behaviors in female mice because chronic social defeat stress protocol cannot successfully induce depression-like behaviors in C57BL/6J female mice. A recent report shows that C57BL/6 mice, one of the most widely used mouse strains, are resistant to the commonly used CUMS protocol due to the variety of genetically modified lines. A recently revised, eight-week CUMS protocol has been developed and used to induce depression-like behaviors in C57BL/6 mice. Interestingly, male and female rodents are differentially affected by CUMS, depending on the behavioral and neurobiological markers that are being measured.

3.3. Chronic Social Defeat Stress (CSDS)

CSDS is one of the most frequently used rodent models for depression and has been used to induce depression-like behaviors in mice such as social avoidance and anhedonia. During each defeat period, an intruder, a male C57BL/6J mouse, is allowed to interact for 10 minutes with an aggressive and large CD1 mouse during which the intruder is rapidly investigated, attacked, and defeated by the resident CD-1 mouse. The experimental C57BL/6J mice are exposed to a different resident aggressor for 10 minutes each day for 10 consecutive days. On the one hand, after completing the social defeats, 30% of animals do not show depression-like behaviors known as “resilient,” a positive adaptation in the face of stress, threat, or severe adversity. On the other hand, a majority of animals (70%) develop depression-like behaviors known as “susceptible.” A disadvantage of this model is that it is limited in studying only male mice because female C57BL/6J mice are not easily defeated by CD-1 mice. This model has been widely used to induce depression-like behaviors and study the molecular mechanisms underlying depression. This model is also used to induce depression-like behaviors in rats.

4.1. Hippocampus (Table 1)

The hippocampus plays an important role in learning and memory and is particularly sensitive to stress and glucocorticoids. Rodent hippocampus contains high levels of glucocorticoid receptors (GRs) and mineralocorticoid-like receptors (MRs). The affinity of MR for corticosterone is 6- to 10-fold higher than that of GR, but it is GR that is activated after stress and is involved in its feedback action on stress-induced neural plasticity. Chronic stress decreases GR expression or its numbers and finally alters the balance of GR/MR in the male hippocampus, which is thought to be a protective mechanism against the damaging effects of chronic stress. Chronic exposure of male rats to glucocorticoids induces depression-like behaviors and causes the synaptic deficits in the hippocampus. A recent report shows that GRs, acting via MR, decrease resilience to stress via downregulation of mGlu2 receptors in mice during CUMS. Chronic stress and glucocorticoids impair hippocampal function, which in turn contributes to the HPA axis dysregulation. The blunting of the feedback mechanism is believed to underlie sustained high levels of glucocorticoids in some depressed patients. People with depression have a significantly smaller hippocampus than healthy individuals, which may result from a decrease in dendritic arbors and spine density in hippocampal neurons. Hippocampal atrophy in depressed patients is associated with depression severity.

CA1 and CA3 Dendrites. Many structural and functional studies show that dendritic retraction or atrophy, characterized by both reduction in total dendritic length and a simplification of dendritic arbors, is found in the dendrites of CA3 pyramidal neurons but not the dendrites of CA1 pyramidal neurons in response to CUMS or CRS (Table 1). Therefore, CA3 dendrites are more sensitive to chronic stress than CA1 dendrites. The different sensitivity of CA1 and CA3 to chronic stress may result from the differences between these two regions in afferents/efferents, the levels of GRs, NMDA receptors, 5-HT receptors, and GABA inhibitory tones. GR levels are higher in the CA1 region than the CA3 region, where the receptors are activated by stress hormone corticosteroids. In addition, it has been repeatedly shown that apical dendrites of CA3 pyramidal neurons are more susceptible to the effects of sustained CRS than CA3 basal dendrites. Dendritic retraction in apical but not basal dendrites of CA3 pyramidal neurons is found after CUMS, chronic psychosocial stress, and CRS. CRS-induced depression-like behaviors and CA3 dendritic atrophy are not permanent but recovered to control levels after certain stress-free period following the end of CRS procedure. Importantly, CA3 dendritic retraction induced by CRS requires corticosterone secretion and intact NMDAR function. Treatments of chronically stressed rats with either the steroid synthesis blocker cyanoketone or competitive NMDA receptor antagonist (CGP 43487) blocked CRS-induced dendritic retraction. Similar to CUMS, rats usually require three weeks to develop depression-like behaviors and CA3 apical dendritic atrophy because only 21 days, but not 7 to 13 days of CRS, induces reversible impairments of spatial memory performance and CA3 apical dendritic atrophy. In addition, atrophy of apical dendrites, but not basal dendrites of CA3 pyramidal neurons, is found after chronic exposure to elevated glucocorticoid levels, which mimics chronic stress. Chronic stress-induced hippocampal CA3 dendritic retraction and elevated glucocorticoid release contribute to impaired spatial memory.

CA3 Dendritic Spines. Chronic stress-induced alterations of spine density in CA3 pyramidal neurons depend on stressor types, animal species, sex, and the duration of stress. CRS causes either a decrease, an increase, or no change in the spine density in the dendrites of male rat CA3 pyramidal neurons. CRS-induced loss of synapses in male rat CA3 apical dendrites can be recovered following water maze training. One report shows that CRS causes a decrease in dendritic spine density, especially in thin and mushroom spines in mouse CA1 pyramidal neurons, but does not affect total spine density in mouse CA3 pyramidal neurons, due to increased stubby spine density and decreased thin and mushroom spine density. The degree of stress-induced spine loss in CA3 pyramidal neurons correlates significantly with the memory defects and loss of LTP in mice. In comparison with CRS, both 21-day CUMS and 30-day CUMS decrease spine density in male rat CA3 pyramidal neurons, whereas 14-day CUMS increases spine density in male mouse CA3 pyramidal neurons, which is consistent with our report that two-week CUMS enhances LTP induction in CA3-CA1 synapses in male rat hippocampus. Psychosocial stress (1 h/day for 28 days) does not affect spine density in CA3 pyramidal neurons of male tree shrews.

CA1 Dendritic Spines. CA1 is a hippocampal region crucial for long-term memory. In comparison with CA3 pyramidal neurons, chronic stress-induced changes in spine density in CA1 pyramidal neurons are less characterized. Stress affects spine density in CA1 pyramidal neurons in a sex-dependent manner. Acute stress (30, 1 sec, 1 mA, 60 Hz shocks to the tail) increases spine density in the apical dendrites of male hippocampal CA1 pyramidal neurons but decreases it in the same area of female hippocampus. These increases and decreases in spine density are dependent on NMDA receptor activation. Similar to acute stress, the same CRS regimen causes a decrease in spine density in the apical dendrites of hippocampal CA1 pyramidal neurons in male rat and male mouse but causes an increase in spine density in the same region in female rats. One recent study shows that CRS decreases spine density in basal dendrites, while it increases apical dendritic arbors in the CA1 pyramidal neurons of the ventral hippocampus in female but not in male rats. In contrast to female rats, female mice show a decrease in spine density in CA1 pyramidal after exposure to same 21-day CRS. Additionally, an ultrastructural study of CA1 synapses shows that 21-day CRS causes an increase in the size of the postsynaptic density in male rat CA1. Similar to CRS, CUMS also causes a decrease in spine density in the dendrites of CA1 pyramidal neurons in male rat. Stress-induced increase in spine density in the apical dendrites of CA1 pyramidal neurons in female rat and same stress-induced decrease in spine density in the same area in male rat are completely prevented by NMDA receptor antagonist CPP, but exposure of NMDA receptor antagonist CPP to the stress procedure does not affect corticosterone levels or the corticosterone response to stress, suggesting a key role of NMDA receptor activation in stress-induced increases or decreases in spine density. Similar to sex-dependent alterations of dendritic spines induced by both acute stress and CRS in hippocampal CA1 pyramidal neurons, there is a sex difference in CRS-induced changes in hippocampal-dependent spatial learning and memory. CRS impairs spatial learning and memory in males but not in females. Furthermore, recent studies suggest that CUMS-induced glutamatergic dysfunction in excitatory temporoammonic- (TA-) CA1 synapses of the hippocampus serves as an underlying cause of depression. This suggests that restoring spine loss or excitatory synaptic dysfunction in the hippocampus could be a novel therapeutic target for depression. Similar to CUMS, chronic exposure of male rats to corticosterone for 3-4 weeks induces depression-like behaviors and causes a decrease in AMPAR-mediated excitation at temporoammonic-CA1 synapses accompanied by decreased expression of GluR1 protein. Blocking CUMS-induced increase of corticosterone during CUMS with the corticosterone synthesis inhibitor metyrapone prevents stress-induced depression-like behaviors. Similar to male rats, exposure of male mice to 35-day corticosterone treatments shows anxiety/depression-like behaviors, accompanied by a reduction in spine density, mainly in thin and stubby spines but not in mushroom spines in CA1 pyramidal neurons. Mushroom spines are more stable and resistant to corticosterone or CRS. Chronic corticosterone-induced decreases in spine density in the hippocampal CA1 pyramidal neurons and depression-like behaviors recover to normal levels concomitantly after 25-day treatment with fluoxetine. These studies suggest that corticosterone secreted during stress plays a key role in chronic stress-induced depression-like behaviors, dysfunction of excitatory synapses, and alteration of dendritic spines in the hippocampus; rescuing chronic stress-induced loss of dendritic spines and/or synaptic dysfunction may rescue depression-like behaviors.

4.2. Prefrontal Cortex (PFC) (Table 2)

The medial PFC (mPFC), an information processing center, is often divided into the anterior cingulate, prelimbic (PL), and infralimbic (IL) subregions. These subregions are different in structure and function. The mPFC plays a critical role in the integration of cognitive and emotionally relevant information, modulation of subcortical systems, and attention. The mPFC expressing high levels of glucocorticoid receptors is a target site for glucocorticoids and plays an important role in the regulation of the response of HPA axis to stress and antidepressant response. It is widely reported that the mPFC volume is decreased in a subset of depressed patients. However, a recent report shows that the decreased volume of the mPFC is found in male but not in female depressed patients. The decreased volume of the mPFC in depressed patients is in line with decreased expression of synaptic-function-related genes and loss of synapses in the mPFC of subjects with major depression disorder. In addition, glial cell loss, reductions in the density and size of neurons in the postmortem mPFC of subjects with major depression, may contribute to pathology of depression. Animal studies show that the retraction of apical dendrites of pyramidal neurons in the mPFC induced by chronic stress is accompanied by alterations in fear conditioning and extinction. CRS-induced dendritic retraction and spine loss in the hippocampal and mPFC neurons are accompanied by cognitive impairments, which are mediated by each respective structural alteration.

It is well documented that CRS results in a retraction of the distal part of apical dendritic arbors of layers II/III pyramidal cells and a decrease in spine density on those neurons in the mPFC of male rats, which is similar to that found in hippocampal CA3 region. The pattern of CRS-induced dendritic reorganization is similar to that seen after daily corticosterone injections. CRS also alters spine morphology with an overall decrease in mean dendritic spine volume and surface area, a reduction in large mushroom spine density, and an increase in small thin spine density in the mPFC of male rats. These findings suggest failure of the spines to mature and stabilize following CRS. One conflicting study, however, reports that CRS-induced decrease in spine density in the male rat mPFC is characterized by a decrease in thin and stubby spine density without affecting mushroom spine density.

CRS causes a reduction of length and branch number in the apical dendrites of the neurons in the mPFC of young (3 months) and aged (20 months) male rats. Surprisingly, CRS-induced retraction of apical dendrites, however, is reversed with recovery in young (3 months) but not aged (20 months) animals. In young rats, CRS results in dendritic spine loss and alters the patterns of spine morphology. In contrast, CRS does not affect spine density and spine shape in aged animals, showing that dendritic spines become progressively less plastic in the aging brain. Interestingly, chronic immobilization stress does not affect spine density in a subpopulation of IL neurons in the mPFC that project to the basolateral amygdala (BLA) in male rats, suggesting this pathway may be particularly resilient against the effects of stress. Randomly selected neurons in the IL of the mPFC, however, show dendritic retraction after CRS. Since most layer II/III neurons project intracortically, the majority of randomly selected pyramidal neurons may be local cortical neurons with no projections to the BLA. An independent study reports that IL neurons, but not PL neurons, in the mPFC are highly sensitive to a brief exposure to stress and the same form of stress impairs fear extinction in mice. However, these IL neurons are putative local cortical neurons without projections to the BLA. A conflicting report shows that CRS causes dendritic retraction in PL neurons of rat mPFC, while this dendritic retraction is prevented by the D1R antagonist SCH23390, and the same D1R antagonist causes dendritic retraction in the PL neurons of the mPFC in unstressed rats. However, the effects of CRS on dendrites in the IL neurons of mPFC are not studied in this report. These results show that dopaminergic transmission in the PL neurons of the mPFC during stress may contribute directly to the CRS-induced retraction of apical dendrites, while dopamine transmission in the absence of stress is important in maintaining normal dendritic morphology. Recent reports show that acute foot-shock stress not only produces an increase in the number of excitatory synapses and docked vesicles in the mPFC, but also induces rapid and sustained increases in spine density accompanied by atrophy of apical dendrites in the PL neurons of the mPFC. Importantly, these synaptic changes induced by acute stress are prevented by chronic antidepressant desipramine treatments. Optogenetic activation of the mPFC exerts potent antidepressant-like effects, showing that the activity of the mPFC may play a key role in the development of depression-like behaviors and antidepressant responses. Similar to hippocampus, alteration of stress-mediated dendritic arbors in the mPFC is sex dependent. CRS causes retraction of apical dendrite arbors in the mPFC in male, while it increases apical dendrite arbors in the female mPFC in which CRS-induced dendritic plasticity is estrogen dependent. Rat mPFC is sexually dimorphic, which is characterized by a bigger and more complex apical dendritic tree in the PL neurons of the mPFC in healthy male rats than that in healthy female rats.

4.3. Orbitofrontal Cortex (OFC)

The OFC, a part of the PFC in the frontal lobes in the brain, is involved in cognitive functions, decision-making, and emotional processing. The studies from neuroimaging and neuropathology show that the OFC is involved in pathophysiology of major depression. Decreases in cortical thickness, neuronal size, neuronal density, and glia densities in the II–IV cortical layers of the OFC are found in subjects with major depression. The decrease in neuronal sizes in layer 3 of the OFC from depressed subjects is confirmed by another postmortem study. Neuroimaging and functional studies also show that patients with major depression have reduced OFC volume and reduced density of pyramidal neurons in layers V and III of the OFC. In contrast, animal studies show that 3-week CUMS increases both the volume of layers II/III in the lateral orbital subregion and the volume of layer II in the ventral orbital subregion of the OFC, which is accompanied by an increase in the length of apical dendrites in the ventral orbital subregion of the OFC. Interestingly, CRS causes a 43% increase in the dendritic arbors in the OFC neurons, an effect opposite to what is observed in the mPFC neurons where the same CRS causes 20% retraction of apical dendritic arbors in layer II/III pyramidal neurons of the mPFC. The mechanisms through which CRS increases dendritic arbors of the OFC are not known. Further studies are needed to explore the discrepancy between the data from imaging analysis or postmortem studies and the findings from animal models. Our recent study showed that 3-week CUMS caused a decrease in spine density in the OFC pyramidal neurons, which was accompanied by both depression-like behaviors and decreased expression of Kalirin-7 and PSD95 in the OFC (Chang Xu, Shu-Chen An, and Xin-Ming Ma, unpublished). Kalirin-7 plays an essential role in maintaining dendritic spine density, size, and synaptic functions. Expression of Kalirin-7 in the hippocampus is decreased by 3-week CUMS. Similar to CUMS, chronic exposure of male mice to corticosterone for 20 days that recapitulates blood corticosterone levels found after CRS exposure in mice also decreases spine density in the OFC neurons, which fails to recover after one week of washout period. This suggests that chronic stress-induced decrease in spine density is not reversible in the OFC neurons. Additional study is required to address this question.

4.4. Amygdala (Table 3)

The amygdala, a structure within the subcortical limbic system, is involved in the processing of emotion and motivation such as fear and anger. The amygdala is also responsible for determining what memories are stored and where they are stored. There are conflicting reports on amygdala volume in major depression. Imaging studies show an increase or decrease or no change in amygdala volume or increased activity of amygdala in patients with major depression. A conflicting MRI study reports a trend towards smaller left amygdala volumes in depressed patients compared with healthy controls. A postmortem study shows that depressed subjects have a larger lateral nucleus and a greater number of total BLA neurovascular cells than controls. There are no differences in the number or density of neurons or glia between depressed and control subjects. To our knowledge, it is not clear whether cell size in BLA is altered in depressed patients.

Animal studies show that chronic stress generally results in an increase in spine density and enhanced dendritic arborization in the amygdala (Table 3). This is in contrast to the hippocampus and PFC (Tables 1 and 2). Acute immobilization also causes an increase in spine density without any effects on dendritic arbors in BLA spiny neurons, showing that these neurons are very sensitive to stress. Amygdala-dependent fear learning is enhanced by CRS in rats. Chronic stress causes an increase in dendritic arborization and spine density in the BLA spiny neurons of male rats and male mice. These neurons are thought to be glutamatergic neurons. In contrast, CRS causes a decrease in spine density in spiny neurons in the medial amygdale, which are GABAergic neurons. CRS-induced increase in dendritic arbors and spine density in the BLA pyramidal neurons and CRS-induced depression-like behavior in wild-type mice are absent in fatty acid amide hydrolase (FAAH) deficient mice suggesting a key role of FAAH in maintaining normal amygdala function in the face of chronic stress. Chronic immobilization stress-induced dendritic hypertrophy in the BLA spiny neurons is not reversible. This is distinct from hippocampal CA3 and mPFC atrophy, which is reversible within the same period of stress-free recovery. A single dose of corticosterone induces dendritic hypertrophy in the BLA accompanied by enhanced anxiety. Chronic exposure of mice to corticosterone for 20 days mimicking chronic stress increases dendritic length and spine density in the BLA. Chronic exposure of rats to corticosterone for 2 weeks causes an increase in the levels of memory-related genes including Arc/Arg3.1 and Egr-1 and enhances the consolidation of fear memory processes in the lateral amygdala. In addition, tianeptine, an antidepressant, exerts the opposite roles in chronic stress-induced synaptic changes in the amygdala and hippocampus.

4.5. Nucleus Accumbens (NAc) (Table 4)

Animal studies indicate that the neuronal circuitry of the PFC-NAc-ventral tegmental area (VTA) underlies drug reward responses and contributes to relapse to cocaine seeking. Excitatory axonal terminals from glutamatergic neurons of the PFC form the synapse onto NAc medium spiny neurons (MSNs), which also receive dopaminergic (DA) inputs from the VTA. The VTA receives GABAergic inputs from the NAc and glutamatergic inputs from the PFC. In addition, The NAc also receives glutamatergic inputs from ventral hippocampus and basolateral amygdala. The NAc serves as a hub of the brain's reward pathways and plays a central role in mood and emotion regulation. Depressive symptoms, such as anhedonia, and depression severity are correlated with reduced NAc volume and reduced NAc responses to rewards in depressed patients. An optogenetic study shows that inhibition of the VTA-NAc projection induces resilience, whereas inhibition of the VTA-mPFC projection enhances susceptibility, highlighting a key role of PFC-NAc-VTA circuitry in the development of depression. Therefore, dysregulation of PFC-NAc-VTA reward circuitry may contribute to the pathophysiology of depression. Similar to the effect of cocaine abuse, chronic stress may alter dendritic spines and synaptic plasticity in the PFC-NAc-VTA circuitry. A recent study, however, reports that chronic social defeat stress- (CSDS-) mediated increase in glutamatergic transmission at the intralaminar thalamus- (ILT-) NAc but not PFC-NAc circuitry mediates stress-induced postsynaptic plasticity on the MSNs and depression-like behaviors in susceptible mice.

The MSNs of dorsal striatum receive not only glutamatergic inputs from the cerebral cortex and the thalamus, but also DA innervation from the midbrain. These MSNs account for >95% of the neurons in the striatum. The dorsal striatum and the NAc are not distinguishable in their populations and expression of DA receptors (DRs, D1R and D2R). Approximately half of the striatal MSNs express the D1R; other half MSNs express the D2R. The degree of D1R/D2R colocalization remains controversial, ranging from 10% to 30%. D1R signaling enhances dendritic excitability and glutamatergic signaling in striatonigral MSNs, while D2R signaling exerts the opposite effect in striatopallidal MSNs (indirect pathway). CRS causes a decrease in AMPAR/NMDAR ratio in the D1R-MSN of the NAc compared to nonstressed control, while it does not affect AMPAR/NMDAR ratios in D2R-MSNs of the NAc. This CRS-induced decrease in the ratio of AMPAR/NMDAR in the D1R-MSN is accompanied by depression-like behaviors, showing a role of NAc D1R-MSNs, at least in part, in the development of depression. This is further supported by two recent reports. One report shows that enhanced activity in D1R-MSNs causes resilient behaviors, while inhibition of these D1R-MSNs induces depression-like behaviors after CSDS. Another report shows that CSDS specifically results in an increase in synaptic strength represented by the increased amplitude of uEPSCs (unitary excitatory postsynaptic currents) in large mushroom spines on D1R-MSNs but decreases synaptic strength on D2R-MSNS mushroom spines in the NAc of resilient mice. CSDS does not affect the uEPSC amplitude in small thin spines on both D1R- and D2R-NAc MSNs in resilient mice. CSDS, however, does not alter synaptic strength in mushroom and thin spines on D1R- or D2R-MSNs in the NAc in susceptible mice. These data show that the NAc D1R-MSN of susceptible mice may be resistant to adaptation and play a critical role in the development of chronic stress-induced depression-like behaviors. In addition, the inhibitor of kappaB kinase (IκK) in the NAc is also a critical regulator of depression-like behavior, and the IκK-nuclear factor kappaB (NFκB) plays a key role in the regulation of synaptic signaling and neuronal morphology in vitro and in vivo. Overexpression of IκK increases thin spine density in the NAc MSNs. CSDS-induced increase in IκK activity in the NAc enhances social avoidance behavior and promotes the formation of thin spines. Inhibition of IκK signaling results in a reversal of CSDS-induced social avoidance behaviors, suggesting that CSDS-induced depression-like behaviors are associated with IκK-mediated increase in thin spine density in the NAc. Interestingly, CSDS-induced increases in stubby spine density and the frequency of mEPSCs in the NAc in susceptible mice are accompanied by an increase in the levels of IκK in the NAc. These results show that CSDS-induced increases in stubby spine density and IκK expression in the NAc are correlated with depression-like behaviors. CSDS-mediated downregulation of Rac1 through an epigenetic mechanism contributes to depression-like behaviors and enhanced formation of stubby spines in the NAc MSNs of susceptible mice. Furthermore, DeltaFosB, a transcription factor, plays an essential role in the mechanism of resilience in mice, supported by evidence that CSDS-mediated induction of DeltaFosB in the NAc is not only necessary and sufficient for resilience in mice, but also required for the antidepressant fluoxetine to reverse depression-like behaviors induced by CSDS. NR2B in the NAc plays a key role in the modulation of CSDS-induced depression-like behaviors and synaptic plasticity. CSDS-induced reduction in NR2B surface expression in the mouse NAc neurons is restored by fluoxetine treatment. Behaviorally, restoration of NR2B loss prevents the behavioral sensitization of mice to chronic stress. Overexpression of DNA methyltransferase (Dnmt3a) increases dendritic spine density in the NAc MSNs. CSDS-induced depression-like behaviors are accompanied by an increase in the Dnmt3a levels in the NAc, suggesting that CSDS-induced depression-like behaviors are positively correlated with increased spine density in the NAc neurons. These studies highlight an important role of the NAc in chronic stress-induced depression-like behaviors. It is possible that stress may differently affect dendritic spines in the D1R-MSNs and D2R-MSNs of the NAc. More studies are required for a better understanding of the roles of D1R-MSNs and D2R-MSNs in chronic stress-induced depression-like behaviors and the underlying mechanisms.

Reduced NAc volume in depressed patients is not in line with the findings from animal models in which stress generally results in an increase in spine density in the NAc MSNs. CSDS causes an increase in spine density and the frequency of mEPSCs in the mouse NAc MSNs. In addition, the shell of the NAc is thought to be a part of the extended amygdala. Chronic stress increases spine density in the neurons of the BLA and the shell of NAc even though these two neuron types are naturally different. The downstream mechanisms of chronic stress-induced spine formation in these two distinct neuron types are not clear.

Taken together, these data show that altered spine density and synaptic plasticity in the NAc MSNs are correlated with depression-like behaviors induced by chronic stress, which may be a target for developing the novel treatment strategies for depression.

5. The Mechanisms of Chronic Stress-Induced Alterations in Dendritic Spines

The molecular mechanisms underlying spine loss and dendritic retraction induced by chronic stress in the hippocampus and PFC as well as enhanced spine formation found in the amygdala and NAc in chronically stressed animals are not well understood. Expression of several synapse-related genes is decreased in the postmortem PFC of subjects with major depressive disorder. One of these genes is GATA1 (GATA-binding factor 1), a transcriptional repressor that plays a key role in the formation of dendritic spines and dendrite arbor maintenance. Furthermore, a nuclear pore complex protein, nucleoporin p62 (NUP62), and tyrosine phosphorylation of NUP62 play a critical role in CRS-induced dendritic retraction of hippocampal CA3 pyramidal neurons. Many synaptic proteins including Kalirin-7, spinophilin, Homer1, cofilin, Rac-1, cadherin, p-Akt, p-GSK-3β, p-Erk1/2, PKC, NCAM, PSA-NCAM, SNAP-25, SNAP-29, VAMP1/2, syntaxin 1A, synaptophysin, synapsin 1, Vglut2, GluR1, GluR2, NR1, NR2A, NR2B, PSD95, αCaMKII, melanocortin 4 receptors, CRH receptor 1, and P190RhoGAP play an important role in the regulation of the spine formation and/or synaptic plasticity; expression of these synaptic proteins in the brain is altered by chronic stress, and these proteins may play a key role in chronic stress-induced both depression-like behaviors and spine alterations (Table 1–4). In addition, chronic stress-induced alterations of several signal transduction pathways including cAMP-PKA-CREB, cAMP-ERK1/2-CREB, cAMP-PKA, Ras-ERK, PI3K-Akt, TNFα-Nfκb, GSK-3β, mTOR, and CREB may be also associated with chronic stress-induced spine loss or increase in certain brain areas. A recent report shows that the Homer1/mGluR5 complex is involved in the development of CSDS-induced depression-like behaviors, suggesting a role of this complex in chronic stress-mediated spine plasticity. Presynaptic mGlu2 receptors play a key role in CUMS-induced depression-like behaviors in male susceptible mice. The rapid antidepressant-like properties of ketamine, an NMDA receptor antagonist, result from increased synaptic signaling proteins and increased number and function of new spine synapses via activating the mammalian target of rapamycin (mTOR) pathway in the rat mPFC and hippocampus. S6K1, a key mediator of activity-dependent synaptic protein synthesis, is the downstream of mTORC1 and plays a critical role in CUMS-induced depression-like behaviors. Postmortem studies show that the levels of NR2A, NR2B, mGLuR5, PSD-95, and mTOR as well as the levels of S6K, eIF4B, and p-eIF4B, the core downstream signaling targets of mTOR, are decreased in the PFC of depressed patients. These studies suggest that mTOR signaling is a promising target for the development of novel antidepressant drugs.

Taken together, understanding chronic stress- and/or depression-induced alterations in dendritic spines, synapse plasticity, synaptic proteins, and their upstream/downstream signaling pathways may pave the path for developing efficiency therapeutic strategies for depression. The search for the mechanisms through which chronic stress alters dendritic spines or synapse numbers in different brain regions should be a major future direction.

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    Nimchinsky E. A., Sabatini B. L., Svoboda K. Structure and function of dendritic spines. Annual Review of Physiology. 2002;64:313-353.

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    Ma X.-M., Huang J., Wang Y., Eipper B. A., Mains R. E. Kalirin, a multifunctional Rho guanine nucleotide exchange factor, is necessary for maintenance of hippocampal pyramidal neuron dendrites and dendritic spines. Journal of Neuroscience. 2003;23(33):10593-10603.

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    Sala C., Segal M. Dendritic spines: the locus of structural and functional plasticity. Physiological Reviews. 2014;94(1):141-188.

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    Petrak L. J., Harris K. M., Kirov S. A. Synaptogenesis on mature hippocampal dendrites occurs via filopodia and immature spines during blocked synaptic transmission. Journal of Comparative Neurology. 2005;484(2):183-190.

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    Segal M. Dendritic spines for neuroprotection: a hypothesis. Trends in Neurosciences. 1995;18(11):468-471.

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    Noguchi J., Matsuzaki M., Ellis-Davies G. C. R., Kasai H. Spine-neck geometry determines NMDA receptor-dependent Ca2+ signaling in dendrites. Neuron. 2005;46(4):609-622.

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    Bourne J. N., Harris K. M. Balancing structure and function at hippocampal dendritic spines. Annual Review of Neuroscience. 2008;31:47-67.

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    Radley J. J., Sisti H. M., Hao J., et al. Chronic behavioral stress induces apical dendritic reorganization in pyramidal neurons of the medial prefrontal cortex. Neuroscience. 2004;125(1):1-6.

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    Fénelon K., Xu B., Lai C. S., et al. The pattern of cortical dysfunction in a mouse model of a schizophrenia-related microdeletion. The Journal of Neuroscience. 2013;33(37):14825-14839.

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    Penzes P., Cahill M. E., Jones K. A., VanLeeuwen J.-E., Woolfrey K. M. Dendritic spine pathology in neuropsychiatric disorders. Nature Neuroscience. 2011;14(3):285-293.

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    Chen Y., Kramár E. A., Chen L. Y., et al. Impairment of synaptic plasticity by the stress mediator CRH involves selective destruction of thin dendritic spines via RhoA signaling. Molecular Psychiatry. 2013;18(4):485-496.

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    von Bohlen und Halbach O. Structure and function of dendritic spines within the hippocampus. Annals of Anatomy. 2009;191(6):518-531.

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    Rajkowska G., Stockmeier C. A. Astrocyte pathology in major depressive disorder: insights from human postmortem brain tissue. Current Drug Targets. 2013;14(11):1225-1236.

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    Czéh B., Simon M., Schmelting B., Hiemke C., Fuchs E. Astroglial plasticity in the hippocampus is affected by chronic psychosocial stress and concomitant fluoxetine treatment. Neuropsychopharmacology. 2006;31(8):1616-1626.

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    Rocher C., Spedding M., Munoz C., Jay T. M. Acute stress-induced changes in hippocampal/prefrontal circuits in rats: effects of antidepressants. Cerebral Cortex. 2004;14(2):224-229.

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    Castreń E. Neuronal network plasticity and recovery from depression. JAMA Psychiatry. 2013;70(9):983-989.

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    Christoffel D. J., Golden S. A., Russo S. J. Structural and synaptic plasticity in stress-related disorders. Reviews in the Neurosciences. 2011;22(5):535-549.

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    Duman R. S. Pathophysiology of depression and innovative treatments: remodeling glutamatergic synaptic connections. Dialogues in Clinical Neuroscience. 2014;16(1):11-27.

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    Popoli M., Yan Z., McEwen B. S., Sanacora G. The stressed synapse: the impact of stress and glucocorticoids on glutamate transmission. Nature Reviews Neuroscience. 2012;13(1):22-37.

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    Cook S. C., Wellman C. L. Chronic stress alters dendritic morphology in rat medial prefrontal cortex. Journal of Neurobiology. 2004;60(2):236-248.

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    Radley J. J., Rocher A. B., Miller M., et al. Repeated stress induces dendritic spine loss in the rat medial prefrontal cortex. Cerebral Cortex. 2006;16(3):313-320.

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    Liston C., Miller M. M., Goldwater D. S., et al. Stress-induced alterations in prefrontal cortical dendritic morphology predict selective impairments in perceptual attentional set-shifting. Journal of Neuroscience. 2006;26(30):7870-7874.

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    Radley J. J., Rocher A. B., Rodriguez A., et al. Repeated stress alters dendritic spine morphology in the rat medial prefrontal cortex. Journal of Comparative Neurology. 2008;507(1):1141-1150.

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    Perez-Cruz C., Simon M., Czéh B., Flügge G., Fuchs E. Hemispheric differences in basilar dendrites and spines of pyramidal neurons in the rat prelimbic cortex: activity- and stress-induced changes. European Journal of Neuroscience. 2009;29(4):738-747.

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    Hains A. B., Vu M. A. T., Maciejewski P. K., Van Dyck C. H., Gottron M., Arnsten A. F. T. Inhibition of protein kinase C signaling protects prefrontal cortex dendritic spines and cognition from the effects of chronic stress. Proceedings of the National Academy of Sciences of the United States of America. 2009;106(42):17957-17962.

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    Goldwater D. S., Pavlides C., Hunter R. G., et al. Structural and functional alterations to rat medial prefrontal cortex following chronic restraint stress and recovery. Neuroscience. 2009;164(2):798-808.

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    Garrett J. E., Wellman C. L. Chronic stress effects on dendritic morphology in medial prefrontal cortex: sex differences and estrogen dependence. Neuroscience. 2009;162(1):195-207.

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    Bloss E. B., Janssen W. G., McEwen B. S., Morrison J. H. Interactive effects of stress and aging on structural plasticity in the prefrontal cortex. The Journal of Neuroscience. 2010;30(19):6726-6731.

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    Bloss E. B., Janssen W. G., Ohm D. T., et al. Evidence for reduced experience-dependent dendritic spine plasticity in the aging prefrontal cortex. The Journal of Neuroscience. 2011;31(21):7831-7839.

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    Müller H. K., Wegener G., Popoli M., Elfving B. Differential expression of synaptic proteins after chronic restraint stress in rat prefrontal cortex and hippocampus. Brain Research. 2011;1385:26-37.

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    Yu H., Wang D.-D., Wang Y., Liu T., Lee F. S., Chen Z.-Y. Variant brain-derived neurotrophic factor Val66met polymorphism alters vulnerability to stress and response to antidepressants. Journal of Neuroscience. 2012;32(12):4092-4101.

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    Gilabert-Juan J., Castillo-Gomez E., Guirado R., Moltó M. D., Nacher J. Chronic stress alters inhibitory networks in the medial prefrontal cortex of adult mice. Brain Structure and Function. 2013;218(6):1591-1605.

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    Lin G. L., Borders C. B., Lundewall L. J., Wellman C. L. D1 receptors regulate dendritic morphology in normal and stressed prelimbic cortex. Psychoneuroendocrinology. 2015;51:101-111.

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    Yuen E. Y., Wei J., Liu W., Zhong P., Li X., Yan Z. Repeated stress causes cognitive impairment by suppressing glutamate receptor expression and function in prefrontal cortex. Neuron. 2012;73(5):962-977.

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    Banasr M., Valentine G. W., Li X.-Y., Gourley S. L., Taylor J. R., Duman R. S. Chronic unpredictable stress decreases cell proliferation in the cerebral cortex of the adult rat. Biological Psychiatry. 2007;62(5):496-504.

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    Dias-Ferreira E., Sousa J. C., Melo I., et al. Chronic stress causes frontostriatal reorganization and affects decision-making. Science. 2009;325(5940):621-625.

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    Li N., Liu R.-J., Dwyer J. M., et al. Glutamate N-methyl-D-aspartate receptor antagonists rapidly reverse behavioral and synaptic deficits caused by chronic stress exposure. Biological Psychiatry. 2011;69(8):754-761.

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    Shansky R. M., Hamo C., Hof P. R., McEwen B. S., Morrison J. H. Stress-induced dendritic remodeling in the prefrontal cortex is circuit specific. Cerebral Cortex. 2009;19(10):2479-2484.

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    Kang H. J., Voleti B., Hajszan T., et al. Decreased expression of synapse-related genes and loss of synapses in major depressive disorder. Nature Medicine. 2012;18(9):1413-1417.

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    Seib L. M., Wellman C. L. Daily injections alter spine density in rat medial prefrontal cortex. Neuroscience Letters. 2003;337(1):29-32.

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    Izquierdo A., Wellman C. L., Holmes A. Brief uncontrollable stress causes dendritic retraction in infralimbic cortex and resistance to fear extinction in mice. The Journal of Neuroscience. 2006;26(21):5733-5738.

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    Chocyk A., Bobula B., Dudys D., et al. Early-life stress affects the structural and functional plasticity of the medial prefrontal cortex in adolescent rats. European Journal of Neuroscience. 2013;38(1):2089-2107.

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    Bennur S., Shankaranarayana Rao B. S., Pawlak R., Strickland S., McEwen B. S., Chattarji S. Stress-induced spine loss in the medial amygdala is mediated by tissue-plasminogen activator. Neuroscience. 2007;144(1):8-16.

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    Marcuzzo S., Dall'Oglio A., Ribeiro M. F. M., Achaval M., Rasia-Filho A. A. Dendritic spines in the posterodorsal medial amygdala after restraint stress and ageing in rats. Neuroscience Letters. 2007;424(1):16-21.

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    Sumislawski J. J., Ramikie T. S., Patel S. Reversible gating of endocannabinoid plasticity in the amygdala by chronic stress: a potential role for monoacylglycerol lipase inhibition in the prevention of stress-induced behavioral adaptation. Neuropsychopharmacology. 2011;36(13):2750-2761.

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    Patel S., Kingsley P. J., MacKie K., Marnett L. J., Winder D. G. Repeated homotypic stress elevates 2-arachidonoylglycerol levels and enhances short-term endocannabinoid signaling at inhibitory synapses in basolateral amygdala. Neuropsychopharmacology. 2009;34(13):2699-2709.

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    Qin M., Xia Z., Huang T., Smith C. B. Effects of chronic immobilization stress on anxiety-like behavior and basolateral amygdala morphology in Fmr1 knockout mice. Neuroscience. 2011;194:282-290.

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    Gilabert-Juan J., Castillo-Gomez E., Pérez-Rando M., Moltó M. D., Nacher J. Chronic stress induces changes in the structure of interneurons and in the expression of molecules related to neuronal structural plasticity and inhibitory neurotransmission in the amygdala of adult mice. Experimental Neurology. 2011;232(1):33-40.

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    Pillai A. G., Anilkumar S., Chattarji S. The same antidepressant elicits contrasting patterns of synaptic changes in the amygdala vs hippocampus. Neuropsychopharmacology. 2012;37(12):2702-2711.

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    Abush H., Akirav I. Cannabinoids ameliorate impairments induced by chronic stress to synaptic plasticity and short-term memory. Neuropsychopharmacology. 2013;38(8):1521-1534.

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    Padival M. A., Blume S. R., Rosenkranz J. A. Repeated restraint stress exerts different impact on structure of neurons in the lateral and basal nuclei of the amygdala. Neuroscience. 2013;246:230-242.

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    Padival M., Quinette D., Rosenkranz J. A. Effects of repeated stress on excitatory drive of basal amygdala neurons in vivo. Neuropsychopharmacology. 2013;38(9):1748-1762.

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    Hill M. N., Kumar S. A., Filipski S. B., et al. Disruption of fatty acid amide hydrolase activity prevents the effects of chronic stress on anxiety and amygdalar microstructure. Molecular Psychiatry. 2013;18(10):1125-1135.

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    Vyas A., Bernal S., Chattarji S. Effects of chronic stress on dendritic arborization in the central and extended amygdala. Brain Research. 2003;965(1-2):290-294.

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    Vyas A., Pillai A. G., Chattarji S. Recovery after chronic stress fails to reverse amygdaloid neuronal hypertrophy and enhanced anxiety-like behavior. Neuroscience. 2004;128(4):667-673.

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    Mitra R., Jadhav S., McEwen B. S., Vyas A., Chattarji S. Stress duration modulates the spatiotemporal patterns of spine formation in the basolateral amygdala. Proceedings of the National Academy of Sciences of the United States of America. 2005;102(26):9371-9376.

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    Vyas A., Jadhav S., Chattarji S. Prolonged behavioral stress enhances synaptic connectivity in the basolateral amygdala. Neuroscience. 2006;143(2):387-393.

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    Suvrathan A., Bennur S., Ghosh S., Tomar A., Anilkumar S., Chattarji S. Stress enhances fear by forming new synapses with greater capacity for long-term potentiation in the amygdala. Philosophical Transactions of the Royal Society B: Biological Sciences. 2014;369(1633).

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    Gourley S. L., Swanson A. M., Koleske A. J. Corticosteroid-induced neural remodeling predicts behavioral vulnerability and resilience. Journal of Neuroscience. 2013;33(7):3107-3112.

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    Monsey M. S., Boyle L. M., Zhang M. L., et al. Chronic corticosterone exposure persistently elevates the expression of memory-related genes in the lateral amygdala and enhances the consolidation of a Pavlovian fear memory. PLoS ONE. 2014;9(3).

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    Cui H., Sakamoto H., Higashi S., Kawata M. Effects of single-prolonged stress on neurons and their afferent inputs in the amygdala. Neuroscience. 2008;152(3):703-712.

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    Maroun M., Ioannides P. J., Bergman K. L., Kavushansky A., Holmes A., Wellman C. L. Fear extinction deficits following acute stress associate with increased spine density and dendritic retraction in basolateral amygdala neurons. European Journal of Neuroscience. 2013;38(4):2611-2620.

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    Social instability stress differentially affects amygdalar neuron adaptations and memory performance in adolescent and adult rats · 2014
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    Lim B. K., Huang K. W., Grueter B. A., Rothwell P. E., Malenka R. C. Anhedonia requires MC4R-mediated synaptic adaptations in nucleus accumbens. Nature. 2012;487:183-189.

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    Vialou V., Robison A. J., Laplant Q. C., et al. ΔFosB in brain reward circuits mediates resilience to stress and antidepressant responses. Nature Neuroscience. 2010;13(6):745-752.

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    Jiang B., Wang W., Wang F., et al. The stability of NR2B in the nucleus accumbens controls behavioral and synaptic adaptations to chronic stress. Biological Psychiatry. 2013;74(2):145-155.

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    Christoffel D. J., Golden S. A., Heshmati M., et al. Effects of inhibitor of κB kinase activity in the nucleus accumbens on emotional behavior. Neuropsychopharmacology. 2012;37(12):2615-2623.

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    Christoffel D. J., Golden S. A., Dumitriu D., et al. IκB kinase regulates social defeat stress-induced synaptic and behavioral plasticity. The Journal of Neuroscience. 2011;31(1):314-321.

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    LaPlant Q., Vialou V., Covington H. E., et al. Dnmt3a regulates emotional behavior and spine plasticity in the nucleus accumbens. Nature Neuroscience. 2010;13(9):1137-1143.

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    Golden S. A., Christoffel D. J., Heshmati M., et al. Epigenetic regulation of RAC1 induces synaptic remodeling in stress disorders and depression. Nature Medicine. 2013;19(3):337-344.

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    Christoffel D. J., Golden S. A., Walsh J. J., et al. Excitatory transmission at thalamo-striatal synapses mediates susceptibility to social stress. Nature Neuroscience. 2015;18(7):962-964.

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    Khibnik L. A., Beaumont M., Doyle M., et al. Stress and cocaine trigger divergent and cell type-specific regulation of synaptic transmission at single spines in nucleus accumbens. Biological Psychiatry. 2015.

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    Krishnan V., Han M.-H., Graham D. L., et al. Molecular adaptations underlying susceptibility and resistance to social defeat in brain reward regions. Cell. 2007;131(2):391-404.

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    Rossi S., De Chiara V., Musella A., et al. Chronic psychoemotional stress impairs cannabinoid-receptor-mediated control of GABA transmission in the striatum. The Journal of Neuroscience. 2008;28(29):7284-7292.

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    Warren B. L., Sial O. K., Alcantara L. F., et al. Altered gene expression and spine density in nucleus accumbens of adolescent and adult male mice exposed to emotional and physical stress. Developmental Neuroscience. 2014;36(3-4):250-260.

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    Muhammad A., Kolb B. Mild prenatal stress-modulated behavior and neuronal spine density without affecting amphetamine sensitization. Developmental Neuroscience. 2011;33(2):85-98.

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    Krishnan V., Nestler E. J. Animal models of depression: molecular perspectives. Current Topics in Behavioral Neurosciences. 2011;7(1):121-147.

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    Nestler E. J., Hyman S. E. Animal models of neuropsychiatric disorders. Nature Neuroscience. 2010;13(10):1161-1169.

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    Caldarone B. J., Zachariou V., King S. L. Rodent models of treatment-resistant depression. European Journal of Pharmacology. 2015;753:51-65.

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    Buynitsky T., Mostofsky D. I. Restraint stress in biobehavioral research: recent developments. Neuroscience and Biobehavioral Reviews. 2009;33(7):1089-1098.

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    Ma X.-M., Lightman S. L. The arginine vasopressin and corticotrophin-releasing hormone gene transcription responses to varied frequencies of repeated stress in rats. Journal of Physiology. 1998;510(2):605-614.

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    Martí O., Armario A. Anterior pituitary response to stress: time-related changes and adaptation. International Journal of Developmental Neuroscience. 1998;16(3-4):241-260.

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    No notice
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    Grissom N., Bhatnagar S. Habituation to repeated stress: get used to it. Neurobiology of Learning and Memory. 2009;92(2):215-224.

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    Luine V., Martinez C., Villegas M., Magariños A. M., Mcewen B. S. Restraint stress reversibly enhances spatial memory performance. Physiology and Behavior. 1996;59(1):27-32.

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    Luine V., Villegas M., Martinez C., McEwen B. S. Repeated stress causes reversible impairments of spatial memory performance. Brain Research. 1994;639(1):167-170.

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    Raadsheer F. C., Hoogendijk W. J. G., Stam F. C., Tilders F. J. H., Swaab D. F. Increased numbers of corticotropin-releasing hormone expressing neurons in the hypothalamic paraventricular nucleus of depressed patients. Neuroendocrinology. 1994;60(4):436-444.

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    Parker K. J., Schatzberg A. F., Lyons D. M. Neuroendocrine aspects of hypercortisolism in major depression. Hormones and Behavior. 2003;43(1):60-66.

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    Holsboer F. The corticosteroid receptor hypothesis of depression. Neuropsychopharmacology. 2000;23(5):477-501.

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    Varghese F. P., Brown E. S. The hypothalamic-pituitary-adrenal axis in major depressive disorder: a brief primer for primary care physicians. Primary Care Companion to the Journal of Clinical Psychiatry. 2001;3(4):151-155.

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    Belvederi Murri M., Pariante C., Mondelli V., et al. HPA axis and aging in depression: systematic review and meta-analysis. Psychoneuroendocrinology. 2014;41:46-62.

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    Aboul-Fotouh S. Chronic treatment with coenzyme Q10 reverses restraint stress-induced anhedonia and enhances brain mitochondrial respiratory chain and creatine kinase activities in rats. Behavioural Pharmacology. 2013;24(7):552-560.

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    Chiba S., Numakawa T., Ninomiya M., Richards M. C., Wakabayashi C., Kunugi H. Chronic restraint stress causes anxiety- and depression-like behaviors, downregulates glucocorticoid receptor expression, and attenuates glutamate release induced by brain-derived neurotrophic factor in the prefrontal cortex. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2012;39(1):112-119.

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    Zafir A., Ara A., Banu N. In vivo antioxidant status: a putative target of antidepressant action. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 2009;33(2):220-228.

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    Bravo J. A., Díaz-Veliz G., Mora S., et al. Desipramine prevents stress-induced changes in depressive-like behavior and hippocampal markers of neuroprotection. Behavioural Pharmacology. 2009;20(3):273-285.

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