Glucocorticoid actions on synapses, circuits, and behavior: Implications for the energetics of stress

被引:209
作者
Myers, Brent [1 ]
McKlveen, Jessica M. [1 ]
Herman, James P. [1 ]
机构
[1] Univ Cincinnati, Dept Psychiat & Behav Neurosci, Cincinnati, OH 45237 USA
基金
美国国家卫生研究院;
关键词
Hypothalamo-pituitary-adrenocortical axis; Corticosterone; Prefrontal cortex; Amygdala; Hippocampus; Hypothalamus; Glucocorticoid receptor; Mineralocorticoid receptor; CORTICOTROPIN-RELEASING-FACTOR; MEDIAL PREFRONTAL CORTEX; CENTRAL AMYGDALOID NUCLEUS; LONG-TERM POTENTIATION; PITUITARY-ADRENAL AXIS; HYPOTHALAMIC PARAVENTRICULAR NUCLEUS; ANXIETY-LIKE BEHAVIOR; QUALITY-OF-LIFE; INDUCED CORTICOSTERONE SECRETION; INDUCED NORADRENERGIC ACTIVATION;
D O I
10.1016/j.yfrne.2013.12.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Environmental stimuli that signal real or potential threats to homeostasis lead to glucocorticoid secretion by the hypothalamic-pituitary-adrenocortical (HPA) axis. Glucocorticoids promote energy redistribution and are critical for survival and adaptation. This adaptation requires the integration of multiple systems and engages key limbic-neuroendocrine circuits. Consequently, glucocorticoids have profound effects on synaptic physiology, circuit regulation of stress responsiveness, and, ultimately, behavior. While glucocorticoids initiate adaptive processes that generate energy for coping, prolonged or inappropriate glucocorticoid secretion becomes deleterious. Inappropriate processing of stressful information may lead to energetic drive that does not match environmental demand, resulting in risk factors for pathology. Thus, dysregulation of the HPA axis may promote stress-related illnesses (e.g. depression, PTSD). This review summarizes the latest developments in central glucocorticoid actions on synaptic, neuroendocrine, and behavioral regulation. Additionally, these findings will be discussed in terms of the energetic integration of stress and the importance of context-specific regulation of glucocorticoids. (C) 2014 Published by Elsevier Inc.
引用
收藏
页码:180 / 196
页数:17
相关论文
共 314 条
[1]   Post-training administration of corticosterone enhances consolidation of contextual fear memory and hippocampal long-term potentiation in rats [J].
Abrari, Kataneh ;
Rashidy-Pour, Ali ;
Semnanian, Saeed ;
Fathollahi, Yaghoub .
NEUROBIOLOGY OF LEARNING AND MEMORY, 2009, 91 (03) :260-265
[2]  
Adamec R E, 1990, Neuroreport, V1, P255, DOI 10.1097/00001756-199011000-00022
[3]   Low-dose cortisol for symptoms of posttraumatic stress disorder [J].
Aerni, A ;
Traber, R ;
Hock, C ;
Roozendaal, B ;
Schelling, G ;
Papassotiropoulos, A ;
Nitsch, RM ;
Schnyder, U ;
de Quervain, DJF .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (08) :1488-1490
[4]   Corticosterone exerts site-specific and state-dependent effects in prefrontal cortex and amygdala on regulation of adrenocorticotropic hormone, insulin and fat depots [J].
Akana, SF ;
Chu, A ;
Soriano, L ;
Dallman, MF .
JOURNAL OF NEUROENDOCRINOLOGY, 2001, 13 (07) :625-637
[5]  
Akirav I., 2013, NEUROSCI BIOBEHAV RE
[6]   Chronic unpredictable stress impairs long-term potentiation in rat hippocampal CA1 area and dentate gyrus in vitro [J].
Alfarez, DN ;
Joëls, M ;
Krugers, HJ .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2003, 17 (09) :1928-1934
[7]   Corticosterone and stress reduce synaptic potentiation in mouse hippocampal slices with mild stimulation [J].
Alfarez, DN ;
Wiegert, O ;
Joëls, M ;
Krugers, HJ .
NEUROSCIENCE, 2002, 115 (04) :1119-1126
[8]   Different lateral amygdala outputs mediate reactions and actions elicited by a fear-arousing stimulus [J].
Amorapanth, P ;
LeDoux, JE ;
Nader, K .
NATURE NEUROSCIENCE, 2000, 3 (01) :74-79
[9]   Glucocorticoid release and memory consolidation in men and women [J].
Andreano, JM ;
Cahill, L .
PSYCHOLOGICAL SCIENCE, 2006, 17 (06) :466-470
[10]   Behavioral insights from mouse models of forebrain- and amygdala-specific glucocorticoid receptor genetic disruption [J].
Arnett, Melinda G. ;
Kolber, Benedict J. ;
Boyle, Maureen P. ;
Muglia, Louis J. .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2011, 336 (1-2) :2-5