前列腺素E1和罂粟碱:在狒狒模型中通过99mTc-penogram测量增加阴茎血池的能力的比较研究。

D De Bruin, I C Dormehl, D J Du Plessis, L Jacobs, N Hugo, M Maree
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引用次数: 0

摘要

评估阴茎的动脉血液供应和静脉引流在评估男性阳痿是必不可少的。血管活性药物前列腺素E1和罂粟碱作为海绵内注射,通过影响动脉血供和静脉引流引起人类阴茎勃起。这些药物被用于正常狒狒和血管受损狒狒,使用99mTc-penogram来量化阴茎的血管状态。通过结扎阴茎,改变阴茎的血液供应,从而影响血管供应。结果显示,与前列腺素E1组相比,罂粟碱组与前列腺素E1组相比,其对阴茎血池的影响更为显著,但差异不显著(P < 0.05)。在血管受损的狒狒中,这种作用甚至更强(P < 0.05),因此可以推测,不排除罂粟碱后阴茎勃起的发生。前列腺素E1之后更一致的血管活性反应似乎确立了它作为海绵体内注射药物的优越性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prostaglandin E1 and papaverine: a comparative study on the ability to increase the penile bloodpool as measured by the 99mTc-penogram in the baboon model.

The evaluation of arterial blood supply and venous drainage of the penis is essential in assessing the impotent male. The vaso-active drugs prostaglandin E1 and papaverine, as intracavernous injections, cause penile erections in humans by influencing the arterial blood supply and venous drainage. These drugs were used in the normal baboon and in vascular compromised baboons using a 99mTc-penogram to quantify the vascular status of the penis. Ligation of the A. Iliaca Interna was performed to change the penile blood supply, thus compromising the vascular supply. It was observed that pre- and post-operatively, the increase in the penile bloodpool was more dramatic although not significantly so (P less than 0.05), but more variable after papaverine than with prostaglandin E1. The effect was even more enhanced (P less than 0.05) in the vascular compromised baboons so that the occurrence of priapism after papaverine can speculatively not be excluded. Also the more consistent vasoactive response after prostaglandin E1 seems to establish it as the superior intracavernous injectable agent.

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