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选择性多巴胺D3受体拮抗剂SB - 277011导致大鼠射精延迟。

Delay of ejaculation induced by SB-277011, a selective dopamine D3 receptor antagonist, in the rat.

作者信息

Clément Pierre, Pozzato Chiara, Heidbreder Christian, Alexandre Laurent, Giuliano Francois, Melotto Sergio

机构信息

Pelvipharm Laboratories, Orsay, France.

Department of Biology, Centre of Excellence in Drug Discovery, GlaxoSmithKline S.p.A., Verona, Italy.

出版信息

J Sex Med. 2009 Apr;6(4):980-988. doi: 10.1111/j.1743-6109.2008.01173.x. Epub 2008 Feb 4.

Abstract

INTRODUCTION

Dopamine (DA) plays a key role in different aspects of the male sexual response, including sexual motivation and arousal, penile erection, and ejaculation. The modalities of action of DA are however unclear, although the various DA receptors may differentially mediate the activity of DA in different aspects of the male sexual response.

AIM

To clarify the role of DA D(3) receptors in the control of the male sexual response.

METHODS

The effects of a highly selective DA D(3) receptors antagonist (SB-277011; intraperitoneal) were tested in experimental paradigms exploring several aspects of the male sexual response in (i) anesthetized rats using 7-hydroxy-N,N-di-n-propylaminotetralin to induce ejaculation and (ii) conscious rats using sexual incentive motivation and mating tests.

MAIN OUTCOME MEASURES

Physiological markers of erection and emission and expulsion phases of ejaculation were measured in anesthetized rats. Behavioral parameters of sexual incentive motivation and mating tests were quantified.

RESULTS

In anesthetized rats, we found that SB-277011 specifically and dose-dependently inhibited the expulsion phase of ejaculation without impairing either emission phase or erection, and this resulted in delayed ejaculation. Administration of SB-277011 had no effect on the spontaneous preference that males displayed for sexually receptive females as shown in sexual incentive motivation test. Delayed ejaculation was confirmed when male rats were administered with the highest dose of SB-277011 (10 mg/kg) in mating test, where males were free to copulate with estrous females. In addition, the refractory period following ejaculation was lengthened in rats treated with SB-277011.

CONCLUSION

As a whole, the present data demonstrate the specific and primary role of D(3) receptors in the expulsion phase of ejaculation and provide preclinical evidence for the investigation of the therapeutic potential of D(3) antagonism for treating premature ejaculation.

摘要

引言

多巴胺(DA)在男性性反应的不同方面发挥着关键作用,包括性动机与唤起、阴茎勃起及射精。然而,尽管各种DA受体可能在男性性反应的不同方面差异介导DA的活性,但其作用方式尚不清楚。

目的

阐明DA D(3)受体在男性性反应控制中的作用。

方法

在探索男性性反应多个方面的实验范式中,测试了一种高选择性DA D(3)受体拮抗剂(SB - 277011;腹腔注射)的作用,实验对象为:(i)使用7 - 羟基 - N,N - 二正丙基氨基四氢萘诱导射精的麻醉大鼠;(ii)使用性动机激励和交配试验的清醒大鼠。

主要观察指标

在麻醉大鼠中测量勃起、射精的发射和排出阶段的生理指标。对性动机激励和交配试验的行为参数进行量化。

结果

在麻醉大鼠中,我们发现SB - 277011特异性且剂量依赖性地抑制射精的排出阶段,而不损害发射阶段或勃起,这导致射精延迟。如性动机激励试验所示,给予SB - 277011对雄性大鼠对性接受雌性的自发偏好没有影响。在交配试验中,当雄性大鼠给予最高剂量的SB - 277011(10 mg/kg)时,射精延迟得到证实,在该试验中雄性大鼠可自由与发情雌性交配。此外,用SB - 277011处理的大鼠射精后的不应期延长。

结论

总体而言,目前的数据证明了D(3)受体在射精排出阶段的特定和主要作用,并为研究D(3)拮抗剂治疗早泄的治疗潜力提供了临床前证据。

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