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α-2 受体阻断对性反应的影响:使用地来喹明(RS15385)的实验研究。

Effects of alpha-2 blockade on sexual response: experimental studies with Delequamine (RS15385).

作者信息

Bancroft J

机构信息

The Kinsey Institute, Indiana University, USA.

出版信息

Int J Impot Res. 2000 Mar;12(S1):S64-S69.

Abstract

The role of alpha-2 receptors and alpha-2 antagonists in central and peripheral mechanisms of sexual response are discussed. It is concluded that the predominant role of the alpha-2 antagonist centrally is to increase arousal which in certain circumstances, is sexual. It is further concluded that the predominant role of the alpha-2 antagonist peripherally is to modulate (block) the norepinephrine (NE)-induced contractility in the smooth muscle of the penis. How the central arousal mechanisms are specifically linked to sexual response is not understood. Experimental studies with a selective alpha-2 antagonist, delequamine, are briefly reviewed and their complex results discussed. Evidence from sleep studies was consistent with delequamine having both central excitatory and inhibitory effects, dependent on dosage. The possibility that men with psychogenic erectile dysfunction might have increased central alpha-2 tone was considered. The apparent loss of responsiveness to the alpha-2 antagonist in older dysfunctional men was discussed. More questions are raised than answered; further research is needed in this area. International Journal of Impotence Research (2000) 12, Suppl 1, S64-S69

摘要

本文讨论了α-2受体和α-2拮抗剂在性反应的中枢和外周机制中的作用。得出的结论是,α-2拮抗剂在中枢的主要作用是增加唤醒,在某些情况下,这种唤醒是性唤醒。进一步得出的结论是,α-2拮抗剂在外周的主要作用是调节(阻断)去甲肾上腺素(NE)诱导的阴茎平滑肌收缩。目前尚不清楚中枢唤醒机制如何具体与性反应相关联。简要回顾了使用选择性α-2拮抗剂地来喹明的实验研究,并讨论了其复杂的结果。睡眠研究的证据表明,地来喹明根据剂量不同,具有中枢兴奋和抑制作用。考虑了患有心因性勃起功能障碍的男性可能存在中枢α-2张力增加的可能性。讨论了老年性功能障碍男性对α-2拮抗剂反应性明显丧失的情况。提出的问题多于回答的问题;该领域需要进一步研究。《国际阳痿研究杂志》(2000年)12卷,增刊1,S64 - S69

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