Regulation of 5-HT receptors and the hypothalamic-pituitary-adrenal axis -: Implications for the neurobiology of suicide

被引:75
作者
López, JF
Vázquez, DM
Chalmers, DT
Watson, SJ
机构
[1] Univ Michigan, Med Ctr, Mental Hlth Res Inst, Dept Psychiat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Med Ctr, Dept Pediat, Div Endocrinol, Ann Arbor, MI 48109 USA
[3] Arena Pharmaceut, San Diego, CA USA
来源
NEUROBIOLOGY OF SUICIDE: FROM THE BENCH TO THE CLINIC | 1997年 / 836卷
关键词
D O I
10.1111/j.1749-6632.1997.tb52357.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Disturbances in the serotonin (5-HT) system is the neurobiological abnormality most consistently associated with suicide. Hyperactivity of the hypothalamic-pituitary-adrenal (HPA) axis is also described in suicide victims. The HPA axis is the classical neuroendocrine system that responds to stress and whose final product, corticosteroids, targets components of the limbic system, particularly the hippocampus. We will review results from animal studies that point to the possibility that many of the 5-HT receptor changes observed in suicide brains may be a result of, or may be worsened by, the HPA over-activity that may be present in some suicide victims. The results of these studies can be summarized as follows: (1) chronic unpredictable stress produces high corticosteroid levels in rats; (2) chronic stress also results in changes in specific 5-HT receptors (increases in cortical 5-HT2A and decreases in hipocampal 5-HT1A and 5-HT1B); (3) chronic antidepressant administration prevents many of the 5-HT receptor changes observed after stress; and (4) chronic antidepressant administration reverses the overactivity of the HPA axis. If indeed 5-HT receptors have a partial role in controlling affective states, then their modulation by corticosteroids provides a potential mechanism by which these hormones may regulate mood. These data may also provide a biological understanding of how stressful events may increase the risk for suicide in vulnerable individuals and may help us elucidate the neurobiological underpinnings of treatment resistance.
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收藏
页码:106 / 134
页数:29
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