The DOI matches its Crossref record; 52 of the 52 references it cites were found in a registry or an index.
Chronic Stress Induces Contrasting Patterns of Dendritic Remodeling in Hippocampal and Amygdaloid Neurons
Open accessAbstract
The hippocampus and the amygdala are essential components of the neural circuitry mediating stress responses. The hippocampus, which provides negative feedback regulation of the stress response, is particularly vulnerable to degenerative changes caused by chronic stress. Unlike the hippocampus, relatively little is known about how stress affects the amygdala and the nature of its role in the stress response. Hence, we examined the effects of two different models of chronic stress on hippocampal and amygdaloid neuronal morphology in rats. In agreement with previous reports, chronic immobilization stress (CIS) induced dendritic atrophy and debranching in CA3 pyramidal neurons of the hippocampus. In striking contrast, pyramidal and stellate neurons in the basolateral complex of the amygdala exhibited enhanced dendritic arborization in response to the same CIS. Chronic unpredictable stress (CUS), however, had little effect on CA3 pyramidal neurons and induced atrophy only in BLA bipolar neurons. These results indicate that chronic stress can cause contrasting patterns of dendritic remodeling in neurons of the amygdala and hippocampus. Moreover, CIS, but not CUS, reduced open-arm activity in the elevated plus-maze. These findings raise the possibility that certain forms of chronic stress, by affecting specific neuronal elements in the amygdala, may lead to behavioral manifestations of enhanced emotionality. Thus, stress-induced structural plasticity in amygdala neurons may provide a candidate cellular substrate for affective disorders triggered by chronic stress.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In the basolateral amygdala (BLA) chronic unpredictable stress also produced dendritic atrophy but chronic immobilization stress instead increased dendritic branching (Banasr and Duman, 2007;Vyas et al, 2002Vyas et al, , 2003)).”
From Neurocircuitry of Mood Disorders (2010) · cites this paper as Vyas et al, 2002
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In animals, chronic stress results in the prolonged release of glucocorticoids and leads to hypertrophy of the amygdala and nucleus accumbens, atrophy of the hippocampus and prefrontal cortex (PFC), and functional impairment of the PFC (44–55).”
From Psychedelics and Other Psychoplastogens for Treating Mental Illness. (2021) · cites this paper as [47]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“enhanced BDNF/TrkB signaling in the amygdala leads to maladaptive plasticity resulting in overactivation of this brain region and exacerbated anxiety and fear responses (47, 198–200)”
From Psychedelics and Other Psychoplastogens for Treating Mental Illness. (2021) · cites this paper as [47]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“By contrast to the PFC and hippocampus, dendrites in the amygdala expand in response to chronic stress exposure112.”
From Stress signalling pathways that impair prefrontal cortex structure and function (2009) · cites this paper as [112]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In contrast to the PFC, chronic stress exposure increases dendritic growth in the amygdala77, thus accentuating the imbalance of amygdala over PFC function.”
From Stress weakens prefrontal networks: molecular insults to higher cognition (2015) · cites this paper as [77]
Experimental — accuracy not yet measured
The cited source says what the claim attributes to it.
In the citing paper
“In the basolateral amygdala (BLA) chronic unpredictable stress also produced dendritic atrophy but chronic immobilization stress instead increased dendritic branching (Banasr and Duman, 2007;Vyas et al, 2002Vyas et al, , 2003)).”
From Neurocircuitry of Mood Disorders (2010) · cites this paper as Vyas et al, 2002
The cited source says what the claim attributes to it.
In the citing paper
“The authors revealed that chronic immobilisation stress in rats resulted in significant dendritic atrophy of apical and basal dendrites of CA3 pyramidal neurons, with a more pronounced loss in apical dendrites.”
From Chronic Stress-Associated Depressive Disorders: The Impact of HPA Axis Dysregulation and Neuroinflammation on the Hippocampus—A Mini Review (2025) · cites this paper as [95]
The cited source says what the claim attributes to it.
In the citing paper
“Animal studies revealed that chronic stress causes atrophy of apical dendrites of pyramidal neurons in the CA3 region of the hippocampus (Magarinos et al. 1996; Vyas et al. 2002; Watanabe et al. 1992).”
From Neurotrophic factors and neuroplasticity pathways in the pathophysiology and treatment of depression (2018) · cites this paper as Vyas et al. 2002
The cited source says what the claim attributes to it.
In the citing paper
“This view is supported by recent evidence that individual brain regions are affected by stress in very different ways.”
From Episodic memory, perceptual memory, and their interaction: Foundations for a theory of posttraumatic stress disorder. (2014) · cites this paper as Vyas, Mitra, Rao, & Chattarji, 2002
The cited source says what the claim attributes to it.
In the citing paper
“a study of neuronal morphology showed that the same stress experience produced dendritic atrophy and debranching in the hippocampus at the same time as producing enhanced dendritic arborization in the amygdala”
From Episodic memory, perceptual memory, and their interaction: Foundations for a theory of posttraumatic stress disorder. (2014) · cites this paper as Vyas, Mitra, Rao, & Chattarji, 2002
In the citing paper
“In rodents, repeated stress results in dendritic atrophy and reduced glial cell counts in hippocampal regions (McEwen and Magarinos, 2001) as well as increased dendritic branching in the basolateral amygdala (Vyas et al., 2002).”
From Individual differences in amygdala-medial prefrontal anatomy link negative affect, impaired social functioning, and polygenic depression risk (2012) · cites this paper as Vyas et al., 2002
In the citing paper
“Specifically, studies of rodents show that stress increases dendritic arborization and spine density of the amygdala, with concomitant increases in anxiety-like behaviors (Vyas et al., 2002; Vyas et al., 2003, Mitra et al., 2005).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“In contrast, stress-induced amygdala morphology and volume changes seem to persist (Vyas et al., 2002, Adamec et al., 2005, Tottenham et al., 2010).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“By contrast, stress results in atrophy of the hippocampus and medial PFC (mPFC) (Magariños et al., 1997, Vyas et al., 2002, Radley et al., 2006).”
From The impact of developmental timing for stress and recovery (2015) · cites this paper as Vyas et al., 2002
In the citing paper
“Neuronal and synaptic remodeling in BLA PNs, along with enhanced glutamatergic transmission, has been repeatedly associated with the negative consequence of stress (14,33,34,40), and prevention of these changes is paralleled by a protection against stress-induced increases in anxiety-like behavior (26,41).”
From Chronic Stress Remodels Synapses in an Amygdala Circuit-Specific Manner (2019) · cites this paper as [14]
In the citing paper
“Repeated stress causes dendritic shortening in medial prefrontal cortex (Sousa et al., 2000; Wellman, 2001; Vyas et al., 2002; Kreibich and Blendy, 2004; Cook and Wellman, 2004; Radley et al., 2004; Brown et al., 2005; Radley et al., 2005)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“but produces dendritic growth in neurons in amygdala (Vyas et al., 2002)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“both acute and chronic stress also increases spine synapse formation in amygdala (Vyas et al., 2002)”
From Central effects of stress hormones in health and disease: understanding the protective and damaging effects of stress and stress mediators (2008) · cites this paper as Vyas et al., 2002
In the citing paper
“Acute stress induces spine synapses in the CA1 region of hippocampus98 and both acute and chronic stress also increases spine synapse formation in amygdala,95-99 but chronic stress decreases it in hippocampus.77”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Repeated stress causes dendritic shortening in medial prefrontal cortex.89-95 but produces dendritic growth in neurons in amygdala,95 as well as in orbitofrontal cortex.96”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Behavioral correlates of remodeling in the prefrontal cortex include impairment in attention set shifting, possibly reflecting structural remodeling in the medial prefrontal cortex.95”
From Protective and damaging effects of stress mediators: central role of the brain (2006) · cites this paper as [95]
In the citing paper
“Additionally, multiple studies have found that chronic stress results in an increase in dendritic arborization and spinogenesis on BLA pyramidal neurons, increasing their intrinsic excitability and afferent stimulation in a manner that correlates with heightened anxiety-like behavior [70–72].”
From Amygdala FAAH and anandamide: mediating protection and recovery from stress (2013) · cites this paper as [70]
In the citing paper
“Acute traumatic stressors were found to cause increased spine density on basolateral amygdale (BlA) neurons and chronic stress leads to the expansion of BlA dendrites.”
From Neurobiological and Systemic Effects of Chronic Stress (2017) · cites this paper as [18]
In the citing paper
“Chronic stress causes dendritic shrinkage not only in CA3 and dentate gyrus neurons of hippocampus but also in medial amygdala and mPFC, while dendrites in BlA and orbitofrontal cortex expand with chronic stress.”
From Neurobiological and Systemic Effects of Chronic Stress (2017) · cites this paper as [18]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The role of the amygdala in fear and anxiety
Davis, M. (1992) · Annual Review of Neuroscience · doi:10.1146/annurev.ne.15.030192.002033 · Cited by 2,357
Neurocircuitry of stress: central control of the hypothalamo–pituitary–adrenocortical axis
Herman, J. P., & Cullinan, W. E. (1997) · Trends in Neurosciences · doi:10.1016/s0166-2236(96)10069-2 · Cited by 2,270
STRESS AND HIPPOCAMPAL PLASTICITY
McEwen, B. S. (1999) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.22.1.105 · Cited by 2,087
Hippocampal atrophy in recurrent major depression
Sheline, Y. I., Wang, P. W., Gado, M. H., Csernansky, J. G., & Vannier, M. W. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.9.3908 · Cited by 1,932
JACOBSON, L., & SAPOLSKY, R. (1991) · Endocrine Reviews · doi:10.1210/edrv-12-2-118 · Cited by 1,739
Cortisol levels during human aging predict hippocampal atrophy and memory deficits
Lupien, S. J., de Leon, M., de Santi, S., Convit, A., Tarshish, C., Nair, N. P. V., Thakur, M., McEwen, B. S., Hauger, R. L., & Meaney, M. J. (1998) · Nature Neuroscience · doi:10.1038/271 · Cited by 1,653
(1995) · American Journal of Psychiatry · doi:10.1176/ajp.152.7.973 · Cited by 1,610
Intrinsic firing patterns of diverse neocortical neurons
Connors, B. W., & Gutnick, M. J. (1990) · Trends in Neurosciences · doi:10.1016/0166-2236(90)90185-d · Cited by 1,440
Swanson, L. W., & Petrovich, G. D. (1998) · Trends in Neurosciences · doi:10.1016/s0166-2236(98)01265-x · Cited by 1,351
Bremner, J. D., Randall, P., Vermetten, E., Staib, L., Bronen, R. A., Mazure, C., Capelli, S., McCarthy, G., Innis, R. B., & Charney, D. S. (1997) · Biological Psychiatry · doi:10.1016/s0006-3223(96)00162-x · Cited by 1,283
Research works printed but not linked: 1
- [28]28. McDonald AJ (1992) Cell types and intrinsic connections of the amyg- dala. In: The amygdala (Aggleton JP, ed), pp 67-96. New York: Wiley.
Cited by
Sorted by citations
Items 901–1,000 of 1,000
An MRI study of amygdala in schizophrenia and psychotic bipolar disorder
Mahon, P. B., Eldridge, H., Crocker, B., Notes, L., Gindes, H., Postell, E., King, S., Potash, J. B., Ratnanather, J. T., & Barta, P. E. (2012) · Schizophrenia Research · doi:10.1016/j.schres.2012.04.005 · Cited by 30
The Development of Stress Reactivity and Regulation in Children and Adolescents
Filetti, C. R., Kane‐Grade, F., & Gunnar, M. R. (2023) · Current Neuropharmacology · doi:10.2174/1570159x21666230808120504 · Cited by 32
Caudle, W. M. (2015) · Physiology & Behavior · doi:10.1016/j.physbeh.2015.09.021 · Cited by 28
Mice overexpressing corticotropin-releasing factor show brain atrophy and motor dysfunctions
Goebel, M., Fleming, S. M., Million, M., Stengel, A., Taché, Y., & Wang, L. (2010) · Neuroscience Letters · doi:10.1016/j.neulet.2010.01.068 · Cited by 26
Pillai, A. G., Anilkumar, S., & Chattarji, S. (2012) · Neuropsychopharmacology · doi:10.1038/npp.2012.135 · Cited by 27
Self-citationMazid, S., Hall, B. S., Odell, S. C., Stafford, K., Dyer, A. G., Kempen, T. A. V., Selegean, J., McEwen, B. S., Waters, E. M., & Milner, T. A. (2016) · Neurobiology of Stress · doi:10.1016/j.ynstr.2016.11.002 · Cited by 25
Tianeptina, un abordaje farmacológico atípico de la depresión
Álamo, C., García‐García, P., Lopez-Munoz, F. J., & Zaragozá, C. (2019) · Revista de Psiquiatría y Salud Mental · doi:10.1016/j.rpsm.2018.09.002 · Cited by 26
Nesin, S. M., Sabitha, K. R., Gupta, A., & Laxmi, T. R. (2019) · Journal of Stroke and Cerebrovascular Diseases · doi:10.1016/j.jstrokecerebrovasdis.2019.02.028 · Cited by 26
DNA methylation in stress and depression: from biomarker to therapeutics
Sales, A. J., Guimarães, F. S., & Joca, S. R. L. (2021) · Acta Neuropsychiatrica · doi:10.1017/neu.2021.18 · Cited by 29
Wang, D., Tian, T., Dong, Q., Xu, X., Yu, H., Wang, Y., & Chen, Z.-Y. (2013) · Hippocampus · doi:10.1002/hipo.22204 · Cited by 26
Fucoidan prevents depression-like behavior in rats exposed to repeated restraint stress
Lee, B., Shim, I., Lee, H., & Hahm, D. (2012) · Journal of Natural Medicines · doi:10.1007/s11418-012-0712-5 · Cited by 26
Bignante, E. A., Paglini, M. G., & Molina, V. A. (2010) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2010.02.007 · Cited by 25
Chronic Stress Decreases Cerebrovascular Responses During Rat Hindlimb Electrical Stimulation
Lee, S., Kang, B., Shin, M., Min, J., Heo, C., Lee, Y.-B., Baeg, E., & Suh, M. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00462 · Cited by 26
Bachis, A., Forcelli, P. A., Masliah, E., Campbell, L. A., & Mocchetti, I. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.01.020 · Cited by 27
The Hypothalamic–Pituitary–Adrenal Axis and Neuroendocrine Responses to Stress
Aguilera, G. (2012) · Elsevier eBooks · doi:10.1016/b978-0-12-375097-6.10008-3 · Cited by 30
Putative neural consequences of captivity for elephants and cetaceans
Jacobs, B., Rally, H., Doyle, C., O’Brien, L., Tennison, M., & Marino, L. (2022) · Reviews in the Neurosciences · doi:10.1515/revneuro-2021-0100 · Cited by 25
Electrophysiological insights into the enduring effects of early life stress on the brain
Ali, I. Y., Salzberg, M. R., French, C. R., & Jones, N. C. (2010) · Psychopharmacology · doi:10.1007/s00213-010-2125-z · Cited by 27
Tianeptine, an atypical pharmacological approach to depression
Álamo, C., García‐García, P., Lopez-Munoz, F. J., & Zaragozá, C. (2019) · Revista de Psiquiatría y Salud Mental (English Edition) · doi:10.1016/j.rpsmen.2018.09.001 · Cited by 25
Environment and early life: Decisive factors for stress-resilience and vulnerability
Hegde, A., & Mitra, R. (2020) · International review of neurobiology · doi:10.1016/bs.irn.2019.12.002 · Cited by 31
Self-citationZhu, L., Shi, H., Chang, L., Zhang, C. C., Si, M., Li, N., & Zhu, D. (2020) · British Journal of Pharmacology · doi:10.1111/bph.15084 · Cited by 25
Sex differences in the delayed impact of acute stress on the amygdala
Gupta, K., & Chattarji, S. (2021) · Neurobiology of Stress · doi:10.1016/j.ynstr.2020.100292 · Cited by 25
Self-citationWhat was learned from studying the effects of early institutional deprivation
Gunnar, M. R., & Bowen, M. (2021) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2021.173272 · Cited by 30
Toledo‐Rodriguez, M., Pitiot, A., Paus, T., & Sandi, C. (2012) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2012.05.006 · Cited by 26
Gillette, R., Miller-Crews, I., Skinner, M. K., & Crews, D. P. (2015) · Frontiers in Genetics · doi:10.3389/fgene.2015.00056 · Cited by 25
Othman, H., Ammari, M., Sakly, M., & Abdelmelek, H. (2017) · Metabolic Brain Disease · doi:10.1007/s11011-017-0016-2 · Cited by 25
Early-life stress induces cognitive disorder in middle-aged mice
Yajima, H., Haijima, A., Khairinisa, M. A., Shimokawa, N., Amano, I., & Takatsuru, Y. (2018) · Neurobiology of Aging · doi:10.1016/j.neurobiolaging.2017.12.021 · Cited by 24
Bürgin, D., Kind, N., Schröder, M., Clemens, V., Fegert, J. M., Eckert, A., Buchheim, A., O’Donovan, A., Boonmann, C., & Schmid, M. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.556486 · Cited by 25
Disruption of Fear Memory Through Dual-Hormone Gene Therapy
Rodrigues, S. M., & Sapolsky, R. M. (2008) · Biological Psychiatry · doi:10.1016/j.biopsych.2008.09.003 · Cited by 25
Greenberg, G. D., van Westerhuyzen, J. A., Bales, K. L., & Trainor, B. C. (2012) · Neuroscience · doi:10.1016/j.neuroscience.2012.04.063 · Cited by 24
Peckham, H. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1103718 · Cited by 36
Kang, J.-S. (2015) · Physical Activity and Nutrition · doi:10.5717/jenb.2015.15080705 · Cited by 24
Glial pathology in neuropsychiatric disorders: a brief review
Mayegowda, S. B., & Thomas, C. (2019) · Journal of Basic and Clinical Physiology and Pharmacology · doi:10.1515/jbcpp-2018-0120 · Cited by 25
Stress Regulation of Sustained Attention and the Cholinergic Attention System
Eck, S. R., Xu, S., Telenson, A. M., Duggan, M. R., Cole, R. D., Wicks, B., Bergmann, J., Lefebo, H., Shore, M. E., Shepard, K. A., et al. (2020) · Biological Psychiatry · doi:10.1016/j.biopsych.2020.04.013 · Cited by 26
Impact of stress on inhibitory neuronal circuits, our tribute to Bruce McEwen
Pérez-Rando, M., Carceller, H., Castillo-Gómez, E., Bueno-Fernández, C., García-Mompó, C., Gilabert‐Juan, J., Guirado, R., Pesarico, A. P., & Nácher, J. (2022) · Neurobiology of Stress · doi:10.1016/j.ynstr.2022.100460 · Cited by 24
Thongrong, S., Surapinit, S., Promsrisuk, T., Jittiwat, J., & Kongsui, R. (2023) · Biomedical Reports · doi:10.3892/br.2023.1602 · Cited by 27
Bourne, A. R., Mohan, G., Stone, M. F., Pham, M., Schultz, C. R., Meyerhoff, J. L., & Lumley, L. A. (2013) · Behavioural Brain Research · doi:10.1016/j.bbr.2013.08.020 · Cited by 25
Evidence for Ancestral Programming of Resilience in a Two-Hit Stress Model
Faraji, J., Soltanpour, N., Ambeskovic, M., Zucchi, F. C. R., Beaumier, P., Kovalchuk, I., & Metz, G. A. S. (2017) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2017.00089 · Cited by 23
Algamal, M., Saltiel, N. A., Pearson, A., Ager, B. J., Burca, I., Mouzon, B., Diamond, D. M., MULLAN, M. J., Ojo, J. O., & Crawford, F. (2019) · Journal of Neurotrauma · doi:10.1089/neu.2018.6314 · Cited by 23
Suppressing the Na+/H+ exchanger 1: a new sight to treat depression
Deng, X., Ji, Z., Xu, B., Guo, L., Xu, L., Qin, T., Feng, L., Ma, Z., Fu, Q., Qu, R., et al. (2019) · Cell Death and Disease · doi:10.1038/s41419-019-1602-5 · Cited by 24
Expansion of hippocampal and amygdala shape in posttraumatic stress and early life stress
Klaming, R., Spadoni, A. D., Veltman, D. J., & Simmons, A. N. (2019) · NeuroImage Clinical · doi:10.1016/j.nicl.2019.101982 · Cited by 25
Faria, M. P., Laverde, C. F., & Nunes‐de‐Souza, R. L. (2020) · Neuropharmacology · doi:10.1016/j.neuropharm.2020.107973 · Cited by 24
Traces of fear in the neural web — Magnetoencephalographic responding to arousing pictorial stimuli
Rockstroh, B. S., & Elbert, T. R. (2010) · International Journal of Psychophysiology · doi:10.1016/j.ijpsycho.2010.01.012 · Cited by 23
Mechanisms Underlying Aluminum Neurotoxicity Related to 14-3-3ζ Protein
Wang, X., Cheng, D., Jiang, W., & Ma, Y. (2018) · Toxicological Sciences · doi:10.1093/toxsci/kfy021 · Cited by 23
Thai, M., Schreiner, M. W., Mueller, B. A., Cullen, K. R., & Klimes‐Dougan, B. (2020) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2020.105123 · Cited by 25
Considering the Microbiome in Stress-Related and Neurodevelopmental Trajectories to Schizophrenia
Hoffman, K. W., Lee, J. J., Corcoran, C. M., Kimhy, D., Kranz, T. M., & Malaspina, D. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00629 · Cited by 24
Pérez, M. Á., Pérez-Valenzuela, C., Rojas‐Thomas, F., Ahumada, J., Fuenzalida, M., & Dagnino‐Subiabre, A. (2013) · Neuroscience · doi:10.1016/j.neuroscience.2013.04.044 · Cited by 23
Monoamine Oxidase A is Required for Rapid Dendritic Remodeling in Response to Stress
Godar, S. C., Bortolato, M., Richards, S. E. V., Li, F. G., Chen, K., Wellman, C. L., & Shih, J. C. (2015) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyv035 · Cited by 23
Wisłowska-Stanek, A., Lehner, M., Skórzewska, A., Krząścik, P., & Płaźnik, A. (2016) · Behavioural Brain Research · doi:10.1016/j.bbr.2016.05.001 · Cited by 25
Effects of gravity changes on gene expression of BDNF and serotonin receptors in the mouse brain
Ishikawa, C., Li, H., Ogura, R., Yoshimura, Y., Kudo, T., Shirakawa, M., Shiba, D., Takahashi, S., Morita, H., & Shiga, T. (2017) · PLoS ONE · doi:10.1371/journal.pone.0177833 · Cited by 23
Vaz, R., Cardoso, A., Serrão, P., Pereira, P. A., & Madeira, M. D. (2018) · Hormones and Behavior · doi:10.1016/j.yhbeh.2017.12.006 · Cited by 24
Clarke, D. J., Chohan, T. W., Kassem, M. S., Smith, K. L., Chesworth, R., Karl, T., Kuligowski, M., Fok, S., Bennett, M. R., & Arnold, J. C. (2018) · Schizophrenia Bulletin · doi:10.1093/schbul/sby029 · Cited by 22
Bittar, T. P., Nair, B. B., Kim, J. S., Chandrasekera, D. N. K., Sherrington, A., & Iremonger, K. J. (2019) · Neuropharmacology · doi:10.1016/j.neuropharm.2019.02.017 · Cited by 25
Wu, H., Huang, Y., Tian, X., Zhang, Z., Zhang, Y., Mao, Y., Wang, C., Yang, S., Liu, Y., Zhang, W., et al. (2019) · Molecular Pain · doi:10.1177/1744806919850383 · Cited by 25
Holliday, E. D., Logue, S. F., Oliver, C. F., Bangasser, D. A., & Gould, T. J. (2019) · Addiction Biology · doi:10.1111/adb.12769 · Cited by 23
Kalynchuk, L. E., & Meaney, M. J. (2003) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2003.09.016 · Cited by 23
Tripathi, S. J., Chakraborty, S., Srikumar, B. N., Raju, T. R., & Rao, B. S. S. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-1057-1 · Cited by 24
Tatekawa, H., Kerr, W. T., Savic, I., Engel, J., & Salamon, N. (2020) · Seizure · doi:10.1016/j.seizure.2019.12.014 · Cited by 22
Aust, S., Stasch, J., Jentschke, S., Alkan Härtwig, E., Koelsch, S., Heuser, I., & Bajbouj, M. (2014) · Hippocampus · doi:10.1002/hipo.22293 · Cited by 22
Musaelyan, K., Aldridge, S., Preez, A. D., Egeland, M. T., Zunszain, P. A., Pariante, C. M., Thuret, S., & Fernandes, C. (2018) · Journal of Psychopharmacology · doi:10.1177/0269881117746902 · Cited by 23
Doubled-Edged Swords in the Biology of Conflict
Sapolsky, R. M. (2018) · Frontiers in Psychology · doi:10.3389/fpsyg.2018.02625 · Cited by 25
Dark, H. E., Harnett, N. G., Goodman, A. M., Wheelock, M. D., Mrug, S., Schuster, M. A., Elliott, M. N., Emery, S. T., & Knight, D. C. (2020) · Cognitive Affective & Behavioral Neuroscience · doi:10.3758/s13415-020-00833-1 · Cited by 27
Higher post-encoding cortisol benefits the selective consolidation of emotional aspects of memory
Cunningham, T. J., Mattingly, S. M., Tlatenchi, A., Wirth, M. M., Alger, S. E., Kensinger, E. A., & Payne, J. D. (2021) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2021.107411 · Cited by 23
da Costa, V. F., Ramírez, J. C. C., Ramírez, S. V., Avalo-Zuluaga, J. H., Baptista‐de‐Souza, D., Canto‐de‐Souza, L., Planeta, C. S., Rico, J. L., & Nunes‐de‐Souza, R. L. (2023) · Frontiers in Integrative Neuroscience · doi:10.3389/fnint.2023.1168640 · Cited by 24
Neigh, G. N., Owens, M. J., Taylor, W. R., & Nemeroff, C. B. (2010) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1038/jcbfm.2010.46 · Cited by 22
Han, T., Lee, J.-K., & Leem, Y. (2014) · Metabolic Brain Disease · doi:10.1007/s11011-014-9624-2 · Cited by 22
Mild blast-related TBI in a mouse model alters amygdalar neurostructure and circuitry
Ratliff, W. A., Mervis, R. F., Citron, B. A., Schwartz, B., Rubovitch, V., Schreiber, S., & Pick, C. G. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.01.020 · Cited by 22
McEwen, B. S., & Karatsoreos, I. N. (2019) · Springer eBooks · doi:10.1007/978-3-030-16996-1_4 · Cited by 25
Cai, Q., Zhu, Z., Li, H., Fan, X., Jia, N., Bai, Z., Song, L., Li, X., & Liu, J. (2006) · Life Sciences · doi:10.1016/j.lfs.2006.10.016 · Cited by 22
Valencia-Flores, K., Sánchez-Castillo, H., Vázquez-León, P., González, P. Z., & Paz, D. B. (2023) · International journal of psychological research · doi:10.21500/20112084.5815 · Cited by 45
Chang, S., Bok, P., Sun, C., Edwards, A., & Huang, G. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006356 · Cited by 21
Michaelson, S. D., Tapia, A. P. M., McKinty, A., Villarroel, H. S., Mackay, J. P., Urban, J. H., & Colmers, W. F. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.2621-19.2020 · Cited by 26
Ross, J. A., & Bockstaele, E. J. V. (2020) · European Journal of Neuroscience · doi:10.1111/ejn.14714 · Cited by 20
Chen, F., Fang, S., Du, Y., Ghosh, A., Reed, M. N., Long, Y., Suppiramaniam, V. D., Tang, S., & Hong, H. (2021) · Aging · doi:10.18632/aging.202501 · Cited by 21
The effect of stress and exercise on the learning performance of horses
Henshall, C., Randle, H., Francis, N., & Freire, R. (2022) · Scientific Reports · doi:10.1038/s41598-021-03582-4 · Cited by 27
Xu, Y., Barish, P. A., Pan, J., Ogle, W. O., & O’Donnell, J. M. (2011) · Methods in molecular biology · doi:10.1007/978-1-61779-458-2_6 · Cited by 21
Oral, E., Kirkan, T. S., Yıldırım, A., Kotan, Z. K., Cansever, Z., Özcan, H., Aliyev, E., & Güleç, M. (2015) · General Hospital Psychiatry · doi:10.1016/j.genhosppsych.2015.03.001 · Cited by 21
Duarte, J. O., Planeta, C. S., & Crestani, C. C. (2014) · International Journal of Developmental Neuroscience · doi:10.1016/j.ijdevneu.2014.11.004 · Cited by 23
Atchley, D., Hankosky, E. R., Gasparotto, K., & Rosenkranz, J. A. (2012) · Behavioural Brain Research · doi:10.1016/j.bbr.2012.03.037 · Cited by 21
Taslimi, Z., Komaki, A., Haghparast, A., & Sarihi, A. (2018) · Basic and Clinical Neuroscience Journal · doi:10.29252/nirp.bcn.9.3.157 · Cited by 21
Vieira, J. O., Duarte, J. O., Ferreira, W. C., & Crestani, C. C. (2018) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2018.07.014 · Cited by 21
Interventions after acute stress prevent its delayed effects on the amygdala
Chakraborty, P., & Chattarji, S. (2019) · Neurobiology of Stress · doi:10.1016/j.ynstr.2019.100168 · Cited by 19
Self-citationClauss, J. A. (2019) · General Psychiatry · doi:10.1136/gpsych-2019-100137 · Cited by 21
Badowska‐Szalewska, E., Klejbor, I., Cecot, T., Spodnik, J. H., & Moryś, J. (2009) · Acta Neurobiologiae Experimentalis · doi:10.55782/ane-2009-1756 · Cited by 21
Effects of post-encoding stress on performance in the DRM false memory paradigmPreprint
Pardilla‐Delgado, E., Alger, S. E., Cunningham, T. J., Kinealy, B. P., & Payne, J. D. (2015) · Learning & Memory · doi:10.1101/lm.039354.115 · Cited by 21
Alteration of somatosensory response in adulthood by early life stress
Takatsuru, Y., & Koibuchi, N. (2015) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2015.00015 · Cited by 20
Dagnino‐Subiabre, A., Muñoz-LLancao, P., Terreros, G., Wyneken, Ú., Díaz‐Véliz, G., Porter, B. A., Kilgard, M. P., Atzori, M., & Aboitiz, F. (2009) · Behavioural Brain Research · doi:10.1016/j.bbr.2009.04.024 · Cited by 20
Bourgin, J., Cachia, A., Boumezbeur, F., Djemaï, B., Bottlaender, M., Duchesnay, É., Mériaux, S., & Jay, T. M. (2015) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2015.02.010 · Cited by 25
Dagnino‐Subiabre, A., Zepeda-Carreño, R., Díaz‐Véliz, G., Mora, S., & Aboitiz, F. (2006) · Brain Research · doi:10.1016/j.brainres.2006.02.118 · Cited by 20
Contextual learning increases dendrite complexity and EphrinB2 levels in hippocampal mouse neurons
Trabalza, A., Colazingari, S., Sgobio, C., & Bevilacqua, A. (2011) · Behavioural Brain Research · doi:10.1016/j.bbr.2011.11.008 · Cited by 20
Basolateral amygdala GABA-A receptors mediate stress-induced memory retrieval impairment in rats
Sardari, M., Rezayof, A., Khodagholi, F., & Zarrindast, M. (2013) · The International Journal of Neuropsychopharmacology · doi:10.1017/s1461145713001363 · Cited by 20
Hung, H.-C., Hsiao, Y.-H., & Gean, P. (2014) · The International Journal of Neuropsychopharmacology · doi:10.1093/ijnp/pyu071 · Cited by 21
Cotinine: A Therapy for Memory Extinction in Post-traumatic Stress Disorder
Mendoza, C., Barreto, G. E., Iarkov, A., Tarasov, V. V., Aliev, G., & Echeverrı́a, V. (2018) · Molecular Neurobiology · doi:10.1007/s12035-018-0869-3 · Cited by 22
The Role of Stress in Bipolar Disorder
Umeoka, E. H. D. L., van Leeuwen, J. M. C., Vinkers, C. H., & Joëls, M. (2020) · Current topics in behavioral neurosciences · doi:10.1007/7854_2020_151 · Cited by 20
Zucchi, F. C. R., Yao, Y., Ilnytskyy, Y., Robbins, J. C., Soltanpour, N., Kovalchuk, I., Kovalchuk, O., & Metz, G. A. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0092130 · Cited by 20
Zucchi, F. C. R., Matthies, N.-F., Badr, N., & Metz, G. A. S. (2010) · Experimental & Translational Stroke Medicine · doi:10.1186/2040-7378-2-18 · Cited by 20
Thamizhoviya, G., & Vanisree, A. J. (2019) · Metabolic Brain Disease · doi:10.1007/s11011-018-0370-8 · Cited by 21
Physical Activity and Individual Cognitive Function Parameters: Unique Exercise-Induced Mechanisms
Frith, E., & Loprinzi, P. D. (2018) · Journal of Cognitive-Behavioral Psychotherapy and Research · doi:10.5455/jcbpr.284071 · Cited by 19
Chen, L., Ke, Y., Ma, H., Gao, L., Zhou, Y., Zhu, H., Liu, H., Zhang, F., & Zhou, W. (2021) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2021.602708 · Cited by 18
Ruan, J., Hu, X., Liu, Y., Han, Z., & Ruan, Q. (2022) · Frontiers in Neuroscience · doi:10.3389/fnins.2022.1046095 · Cited by 20
Separation from a bonded partner alters neural response to inflammatory pain in monogamous rodents
Okuda, T., Osako, Y., Hidaka, C., Nishihara, M., Young, L. J., Mitsui, S., & Yuri, K. (2022) · Behavioural Brain Research · doi:10.1016/j.bbr.2021.113650 · Cited by 7
Metadata
- Authors
- Vyas, A., Mitra, R., Shankaranarayana Rao, B. S., & Chattarji, S.
- Affiliations
- Tata Institute of Fundamental Research (IN)
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2002-08-01
- Volume
- 22
- Issue
- 15
- Pages
- 6810-6818
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- PMC
- PMC6758130
- OpenAlex
- W2136403062
- Semantic Scholar
- 587bd6bf61952d2c4d4fa8f4155737d79006655e
- Cited by
- 1,662
- References
- 51
- Citations by year
- 2026: 42 · 2025: 36 · 2024: 47 · 2023: 50 · 2022: 51 · 2021: 83 · 2020: 94 · 2019: 89 · 2018: 111 · 2017: 87 · 2016: 99 · 2015: 83 · 2014: 90 · 2013: 112 · 2012: 86
- FWCI
- 11.49
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Journal of Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Council of Scientific and Industrial Research, India
- Directorate for Biological Sciences
- National Centre for Biological Sciences
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- chronic stress, dendritic remodeling, hippocampus, amygdala, restraint stress, chronic unpredictable mild stress, CA3 pyramidal cells, basolateral amygdala, stellate neurons, dendritic atrophy, dendritic branching, stress response, structural plasticity, anxiety-like behavior, emotionality, mood disorders
- MeSH terms
- Adrenal Glands, Amygdala, Animals, Anxiety, Body Weight, Chronic Disease, Dendrites, Disease Models, Animal, Hippocampus, Male, Neuronal Plasticity, Neurons, Organ Size, Restraint, Physical, Stress, Physiological, Rats, Wistar, Pyramidal Cells, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review