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通过在离体人海绵体中随时间给予L-精氨酸来优化一氧化氮的产生。

Optimizing nitric oxide production by time dependent L-arginine administration in isolated human corpus cavernosum.

作者信息

Gur Serap, Kadowitz Philip J, Trost Landon, Hellstrom Wayne J G

机构信息

Department of Urology, Tulane Health Sciences Center, New Orleans, Louisiana 70112, USA.

出版信息

J Urol. 2007 Oct;178(4 Pt 1):1543-8. doi: 10.1016/j.juro.2007.05.121. Epub 2007 Aug 16.

Abstract

PURPOSE

We investigated the relaxant effects of repetitive administration of L-arginine, the substrate for nitric oxide, at hourly intervals and elucidated its mechanism of action in human corpus cavernosum.

MATERIALS AND METHODS

Samples of human corpus cavernosum were suspended in an organ chamber for measurements of isometric tension. After precontraction with phenylephrine (10 microM), concentration-response curves were performed for L-arginine at 2-hour intervals (1 to 10 hours). Underlying mechanisms of relaxation were evaluated by inhibitory and stimulatory agents.

RESULTS

After a brief incubation period of 1 to 4 hours L-arginine (0.1 to 1,000 microM) but not D-arginine induced minor changes in HCC. In contrast, when incubation time was increased to 6 to 10 hours L-arginine evoked detectable human corpus cavernosum relaxation proportional to concentration and time. Relaxation was significantly attenuated by the nitric oxide synthase inhibitor L-NAME, the blocker of soluble guanylyl cyclase ODQ and the blocker of small conductance Ca2+ activated K+ channels apamin, and partially by the inducible nitric oxide synthase inhibitor aminoguanidine and the cyclic guanosine 5'-monophosphate dependent protein kinase G inhibitor Rp-8-pCPT-cGMPS. Relaxation was potentiated in the presence of the membrane permeable cyclic guanosine 5'-monophosphate analogue 8-bromo-cyclic guanosine 5'-monophosphate, the Rho-kinase inhibitor Y-27632 and the phosphodiesterase-5 inhibitor sildenafil.

CONCLUSIONS

These observations demonstrate that L-arginine induces slow and prolonged relaxation of human corpus cavernosum. This may occur by restoring the endogenous amino acid pool for nitric oxide synthesis and by nitric oxide-soluble guanylyl cyclase-protein kinase G signaling involving the activation of KCa channels or by inhibiting the up-regulated RhoA/Rho-kinase pathway. The use of sildenafil combined with L-arginine further facilitates erections and it may benefit men with more severe erectile dysfunction.

摘要

目的

我们研究了每隔一小时重复给予一氧化氮底物L-精氨酸的舒张作用,并阐明其在人阴茎海绵体中的作用机制。

材料与方法

将人阴茎海绵体样本悬浮于器官浴槽中以测量等长张力。用去氧肾上腺素(10微摩尔)预收缩后,每隔2小时(1至10小时)绘制L-精氨酸的浓度-反应曲线。通过抑制性和刺激性药物评估舒张的潜在机制。

结果

在1至4小时的短暂孵育期后,L-精氨酸(0.1至1000微摩尔)而非D-精氨酸引起人阴茎海绵体轻微变化。相比之下,当孵育时间增加到6至10小时时,L-精氨酸引起可检测到的人阴茎海绵体舒张,与浓度和时间成比例。一氧化氮合酶抑制剂L-NAME、可溶性鸟苷酸环化酶阻断剂ODQ和小电导钙激活钾通道阻断剂蜂毒明肽可显著减弱舒张作用,诱导型一氧化氮合酶抑制剂氨基胍和环鸟苷酸依赖性蛋白激酶G抑制剂Rp-8-pCPT-cGMPS可部分减弱舒张作用。在存在膜通透性环鸟苷酸类似物8-溴环鸟苷酸、Rho激酶抑制剂Y-27632和磷酸二酯酶-5抑制剂西地那非的情况下,舒张作用增强。

结论

这些观察结果表明,L-精氨酸可诱导人阴茎海绵体缓慢且持久的舒张。这可能通过恢复内源性一氧化氮合成的氨基酸池以及通过一氧化氮-可溶性鸟苷酸环化酶-蛋白激酶G信号传导(涉及钾钙通道激活)或通过抑制上调的RhoA/Rho激酶途径而发生。西地那非与L-精氨酸联合使用可进一步促进勃起,可能对患有更严重勃起功能障碍的男性有益。

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