Sex differences in the neuro-immune consequences of stress: Focus on depression and anxiety

被引:229
作者
Bekhbat, Mandakh [1 ]
Neigh, Gretchen N. [1 ,2 ]
机构
[1] Emory Univ, Dept Physiol, Atlanta, GA 30322 USA
[2] Virginia Commonwealth Univ, Dept Anat & Neurobiol, 1101 E Marshall St, Richmond, VA 23298 USA
关键词
Sex differences; Neuroinflammation; Stress; Female; PITUITARY-ADRENAL AXIS; C-REACTIVE PROTEIN; ADULT MALE-MICE; INFLAMMATORY RESPONSES; PSYCHOLOGICAL STRESS; ADOLESCENT STRESS; BONE-MARROW; ANTIINFLAMMATORY TREATMENT; LEUKOCYTE TRAFFICKING; MICROGLIAL ACTIVATION;
D O I
10.1016/j.bbi.2017.02.006
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Women appear to be more vulnerable to the depressogenic effects of inflammation than men. Chronic stress, one of the most pertinent risk factors of depression and anxiety, is known to induce behavioral and affective-like deficits via neuroimmune alterations including activation of the brain's immune cells, pro-inflammatory cytokine expression, and subsequent changes in neurotransmission and synaptic plasticity within stress-related neural circuitry. Despite well-established sexual dimorphisms in the stress response, immunity, and prevalence of stress-linked psychiatric illnesses, much of current research investigating the neuroimmune impact of stress remains exclusively focused on male subjects. We summarize and evaluate here the available data regarding sex differences in the neuro-immune consequences of stress, and some of the physiological factors contributing to these differences. Furthermore, we discuss the extent to which sex differences in stress-related neuroinflammation can account for the overall female bias in stress-linked psychiatric disorders including major depressive disorder and anxiety disorders. The currently available evidence from rodent studies does not unequivocally support the peripheral inflammatory changes seen in women following stress. Replication of many recent findings in stress related neuroinflammation in female subjects is necessary in order to build a framework in which we can assess the extent to which sex differences in stress-related inflammation contribute to the overall female bias in stress-related affective disorders. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 12
页数:12
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