Italiano G, Calabrò A, Aragona F, Pagano F
Institute of Urology, University of Padua, Italy.
Pharmacol Res. 1995 May;31(5):313-7. doi: 10.1016/1043-6618(95)80037-9.
Experiments were performed to get further insights into the erectogenic mechanism of prostaglandin E1 (PGE1), which was compared to that of papaverine (PAP). PGE1 and PAP were effective in abolishing the contraction induced by N-ethylmaleimide (NEM), an adenylate cyclase blocker. However, preincubation with PGE1 but not with PAP markedly attenuated the amplitude of adrenergic nerve mediated contraction following prolonged electrical field stimulation. Preincubation with PGE1 was ineffective in counteracting the increase in tension due to exogenous norepinephrine. These data together with previous studies corroborate the hypothesis that in the presence of PGE1 a dual erectogenic mechanism takes place in modulating the cyclic-adenosine-monophosphate metabolism of the cavernous smooth muscle cell as well as the release of norepinephrine from the sympathetic terminal.
进行实验以进一步深入了解前列腺素E1(PGE1)的勃起机制,并将其与罂粟碱(PAP)的勃起机制进行比较。PGE1和PAP均可有效消除由腺苷酸环化酶阻滞剂N-乙基马来酰亚胺(NEM)诱导的收缩。然而,用PGE1而非PAP预孵育可显著减弱长时间电场刺激后肾上腺素能神经介导的收缩幅度。用PGE1预孵育对抵消外源性去甲肾上腺素引起的张力增加无效。这些数据与先前的研究共同证实了以下假设:在PGE1存在的情况下,在调节海绵体平滑肌细胞的环磷酸腺苷代谢以及去甲肾上腺素从交感神经末梢的释放过程中会发生双重勃起机制。