Adaikan P G, Ratnam S S
Department of Obstetetrics and Gynecology, National University of Singapore, National University Hospital.
Cardiovasc Intervent Radiol. 1988 Aug;11(4):191-4. doi: 10.1007/BF02577003.
The pharmacologic aspects of erection, including neuropharmacology and erectile responses to exogenous agents, are reviewed. The pharmacology of erection is complex and still incompletely understood. Older evidence suggesting acetylcholine as the primary neurotransmitter has been shown to be insufficient. Our recent experiments utilizing strips of human corpus cavernosum indicate the need to consider the roles of other erectogenic substances, such as vasoactive intestinal polypeptide, endothelium-derived relaxation factor (EDRF), and prostaglandins. From the results of these studies, three stages in the development of an erection are postulated: (1) withdrawal of alpha-adrenergic neuromuscular activity, (2) inhibition of alpha-adrenergic neuromuscular activity by endogenous substances such as prostaglandin E1 and vasoactive intestinal polypeptide, and (3) activation of NANC neurotransmission and direct relaxation of smooth muscle by endogenous substances such as EDRF.
本文综述了勃起的药理学方面,包括神经药理学以及外源性药物引起的勃起反应。勃起的药理学很复杂,目前仍未完全了解。过去认为乙酰胆碱是主要神经递质的证据已被证明是不充分的。我们最近利用人类海绵体条带进行的实验表明,需要考虑其他促勃起物质的作用,如血管活性肠肽、内皮源性舒张因子(EDRF)和前列腺素。根据这些研究结果,推测勃起发展有三个阶段:(1)α-肾上腺素能神经肌肉活动的撤离;(2)内源性物质如前列腺素E1和血管活性肠肽对α-肾上腺素能神经肌肉活动的抑制;(3)非肾上腺素能非胆碱能(NANC)神经传递的激活以及内源性物质如EDRF对平滑肌的直接舒张作用。