Sex Differences in the Serotonergic Influence on the Hypothalamic-Pituitary-Adrenal Stress Axis

被引:77
|
作者
Goel, Nirupa [1 ]
Bale, Tracy L. [1 ]
机构
[1] Univ Penn, Sch Vet Med, Dept Anim Biol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
CORTICOTROPIN-RELEASING-FACTOR; RIBONUCLEIC-ACID EXPRESSION; MESSENGER-RNA LEVELS; PARAVENTRICULAR NUCLEUS; MAJOR DEPRESSION; HPA AXIS; INDUCED ACTIVATION; DECARBOXYLASE GAD; INDUCED INCREASES; RECEPTOR AGONIST;
D O I
10.1210/en.2009-1180
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Appropriate interactions between serotonin (5-HT) and stress pathways are critical for maintaining homeostasis. Dysregulation of hypothalamic-pituitary-adrenal (HPA) stress axis is a common feature in affective disorders in which an involvement of 5-HT neurocircuitry has been implicated in disease vulnerability and treatment responsiveness. Because there is a greater prevalence of affective disorders in women, sex differences in the 5-HTergic influence on stress pathways may contribute to disease disparity. Therefore, our studies compared stress or citalopram-induced corticosterone levels in male and female mice. To determine whether sex-dependent HPA axis responsiveness was mediated by the difference in testosterone levels, testosterone-treated females were also examined. Gene expression patterns in 5-HTergic and stress neurocircuitry were analyzed to determine sites of potential sex differences and mechanisms of testosterone action. As expected, restraint stress corticosterone levels were higher in intact females and were masculinized by testosterone. Interestingly, citalopram administration independent of stress resulted in a greater corticosterone response in females, which was also masculinized by testosterone. Analyses along the 5-HT-HPA axis revealed sex differences including greater pituitary 5-HT receptors and adrenal weights in females. Moreover, in stress-regulatory regions, we found sex differences in glucocorticoid receptor and glutamic acid decarboxylase expression supportive of greater inhibitory modulation and feedback potential in males. Taken together, these data suggest that multiple sites related to 5-HTergic stimulation, corticosterone production, and negative feedback of HPA neurocircuitry combine to produce higher female stress responsiveness. These studies support a potential for sex-specific involvement of 5-HT and stress pathways in the etiology of affective disorders. (Endocrinology 151: 1784-1794, 2010)
引用
收藏
页码:1784 / 1794
页数:11
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