Astrocyte plasticity induced by emotional stress: A new partner in psychiatric physiopathology?

被引:44
作者
Bender, Crhistian L. [1 ]
Calfa, Gaston D. [1 ]
Molina, Victor A. [1 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Farmacol, IFEC CONICET, RA-5000 Cordoba, Argentina
关键词
Acute stress; Anxiety; Astrocytes; Chronic stress; Depression; Plasticity; FIBRILLARY ACIDIC PROTEIN; MAJOR DEPRESSIVE DISORDER; CHRONIC MILD STRESS; CEREBROSPINAL-FLUID LEVELS; PREFRONTAL CORTEX; SYNAPTIC PLASTICITY; RESTRAINT STRESS; FEAR MEMORY; RAT MODEL; MESSENGER-RNA;
D O I
10.1016/j.pnpbp.2015.08.005
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A growing body of evidence has demonstrated that astrocytes play a pivotal role in the normal functioning of the nervous system. This new conceptual framework has set the groundwork to be able to hypothesize that astrocytes could underlie signs and symptoms of mental diseases. Stress is a major risk factor in the etiology of several psychiatric diseases, such as anxiety disorders and depression. Hence, understanding the effects of stress on astrocytes and how these changes contribute to the development of psychiatric endophenotypes is crucial for both a better comprehension of mental illness and for potential targeted treatment of stress-relatedmental disorders. Here, we describe the currently used approaches and recent evidence showing astrocyte alterations induced by chronic and acute stress in animals. In addition, the relevance of these changes in stress-induced behavioral sequelae and human data linking astrocytes with neuropsychiatric disorders related to stress are also discussed. All together, the data indicate that astrocytes are also an important target of stress, with both chronic and acute stressors being able to alter the morphology or the expression of several astrocyte specific proteins in brain areas that are known to play a critical role in emotional processing, such as the prefrontal cortex, hippocampus and amygdala. Furthermore, different lines of evidences suggest that these changes may contribute, at less in part, to the behavioral consequences of stress. (C) 2015 Elsevier Inc. All rights reserved.
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页数:10
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共 114 条
  • [1] Enhanced stress reactivity in nitric oxide synthase type 2 mutant mice: Findings in support of astrocytic nitrosative modulation of behavior
    Abu-Ghanem, Y.
    Cohen, H.
    Buskila, Y.
    Grauer, E.
    Amitai, Y.
    [J]. NEUROSCIENCE, 2008, 156 (02) : 257 - 265
  • [2] Modulation of the autonomic nervous system and behaviour by acute glial cell Gq protein-coupled receptor activation in vivo
    Agulhon, Cendra
    Boyt, Kristen M.
    Xie, Alison Xiaoqiao
    Friocourt, Francois
    Roth, Bryan L.
    McCarthy, Ken D.
    [J]. JOURNAL OF PHYSIOLOGY-LONDON, 2013, 591 (22): : 5599 - 5609
  • [3] Amygdala astrocyte reduction in subjects with major depressive disorder but not bipolar disorder
    Altshuler, Lori L.
    Abulseoud, Osama A.
    Foland-Ross, Lara
    Bartzokis, George
    Chang, Sean
    Mintz, Jim
    Hellemann, Gerhard
    Vinters, Harry V.
    [J]. BIPOLAR DISORDERS, 2010, 12 (05) : 541 - 549
  • [4] [Anonymous], EVID BASED COMPLEMEN, DOI DOI 10.1155/2013/467245
  • [5] Cellular and subcellular sites for noradrenergic action in the monkey dorsolateral prefrontal cortex as revealed by the immunocytochemical localization of noradrenergic receptors and axons
    Aoki, C
    Venkatesan, C
    Go, CG
    Forman, R
    Kurose, H
    [J]. CEREBRAL CORTEX, 1998, 8 (03) : 269 - 277
  • [6] Specific In Vivo Staining of Astrocytes in the Whole Brain after Intravenous Injection of Sulforhodamine Dyes
    Appaix, Florence
    Girod, Sabine
    Boisseau, Sylvie
    Roemer, Johannes
    Vial, Jean-Claude
    Albrieux, Mireille
    Maurin, Mathieu
    Depaulis, Antoine
    Guillemain, Isabelle
    van der Sanden, Boudewijn
    [J]. PLOS ONE, 2012, 7 (04):
  • [7] Tripartite synapses: glia, the unacknowledged partner
    Araque, A
    Parpura, V
    Sanzgiri, RP
    Haydon, PG
    [J]. TRENDS IN NEUROSCIENCES, 1999, 22 (05) : 208 - 215
  • [8] Chronic psychosocial stress and citalopram modulate the expression of the glial proteins GFAP and NDRG2 in the hippocampus
    Araya-Callis, Carolina
    Hiemke, Christoph
    Abumaria, Nashat
    Flugge, Gabriele
    [J]. PSYCHOPHARMACOLOGY, 2012, 224 (01) : 209 - 222
  • [9] Stress signalling pathways that impair prefrontal cortex structure and function
    Arnsten, Amy F. T.
    [J]. NATURE REVIEWS NEUROSCIENCE, 2009, 10 (06) : 410 - 422
  • [10] Glial pathology in an animal model of depression: reversal of stress-induced cellular, metabolic and behavioral deficits by the glutamate-modulating drug riluzole
    Banasr, M.
    Chowdhury, G. M. I.
    Terwilliger, R.
    Newton, S. S.
    Duman, R. S.
    Behar, K. L.
    Sanacora, G.
    [J]. MOLECULAR PSYCHIATRY, 2010, 15 (05) : 501 - 511