生物胺、生殖激素与女性性行为研究进展

Carol Sue Carter , John M. Davis
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引用次数: 32

摘要

根据药理学研究,单胺类,特别是血清素和多巴胺可能会抑制女性的性行为。操纵其他儿茶酚胺和改变胆碱能系统可能促进或抑制女性的性反应。文献中存在一些差异,本综述假设不同程度的雌激素启动可以解释一些观察到的种间和种内差异。其他可能的机制,可能与药物诱导的女性性行为的便利进行了审查。已经清楚地证明,肾上腺分泌对药物引起的女性性接受能力的增加并不是必需的。下丘脑黄体生成素释放激素的变化可能是性接受性药物相关变化的基础。此外,还研究了促进前凸的药物可能与黄体酮具有共同作用机制的相关数据。目前,对后两种假设的直接支持都很少。药物也可能通过改变感觉或自主神经系统来发挥行为作用,但对这些系统的药理作用尚未充分探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Biogenic amines, reproductive hormones and female sexual behavior: A review

Based on pharmacological studies it has been suggested that the monoamines, and in particular serotonin and dopamine may inhibit female sexual behavior. Manipulations of other catecholamines and alterations in cholinergic systems may either facilitate or inhibit female sexual responses. A number of discrepancies exist in the literature and the present review hypothesizes that differential degrees of estrogen priming may explain some of the observed inter- and intraspecific differences. Additional possible mechanisms which may be related to drug induced facilitations of female sexual behavior are reviewed. It has been clearly demonstrated that adrenal secretions are not essential for drug induced increases in female sexual receptivity. It is possible that changes in hypothalamic luteinizing hormone-releasing hormone may underlie drug related changes in sexual receptivity. In addition data relevant to the possibility that drugs which facilitate lordosis may share a common mechanism of action with progesterone are examined. At present there is little direct support for either of the latter hypotheses. Drugs may also exert behavioral effects by changes in sensory or autonomic systems but pharmacological effects on these systems have not been adequately explored.

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