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硝普钠:作为一氧化氮供体在三种物种中的生理效应

Sodium nitroprusside: physiologic effects as a nitric oxide donor in three species.

作者信息

Trigo-Rocha F, Martinez-Piñeiro L, Donatucci C F, Hsu G L, Lue T F, Tanagho E A

机构信息

Department of Urology, University of California School of Medicine, San Francisco 94143-0738, USA.

出版信息

Int J Impot Res. 1995 Mar;7(1):49-56.

PMID:7670593
Abstract

Recent in vitro and in vivo studies have suggested that nitric oxide may be the neurotransmitter responsible for cavernous smooth muscle relaxation and penile erection. Sodium nitroprusside, after combining with different kinds of thiols in the cellular cytoplasm, can effect nitric oxide release. We undertook this study to determine the physiologic response to sodium nitroprusside injection when used to induce and maintain penile erection in three species. Sodium nitroprusside was injected in increasing concentrations into the cavernous tissue of rats, dogs and monkeys. Dosages injected were 10(-4) M, 10(-3) M and 10(-2) M in 10 rats; 10(-4) and 10(-3) M in five dogs and five monkeys. The volume of drug injected was 0.05 ml for the rats and 0.5 ml for dogs and monkeys. The results show a dose-dependent erectile response to sodium nitroprusside injection (mean intracavernous pressure increase of 102.4 cm H2O in dogs, and 98.4 cm H2O in monkeys after injection of 10(-3) M nitroprusside). However, only a slight increase in intracavernous pressure (mean increase 28.4 cm H2O after injection of 10(-2) M of sodium nitroprusside) was noted in rats. The drop in blood pressure was > 15 mmHg in dogs and monkeys, while in rats it varied according to the dose studied. Sodium nitroprusside induced excellent erections in dogs and monkeys with minimal alteration in blood pressure. However, administration in rats resulted in hypotension. Nitroprusside may not be an acceptable nitric oxide donor for the treatment of male erectile dysfunction.

摘要

最近的体外和体内研究表明,一氧化氮可能是负责海绵体平滑肌松弛和阴茎勃起的神经递质。硝普钠在与细胞质中的不同种类硫醇结合后,可促使一氧化氮释放。我们进行这项研究以确定在三种动物中注射硝普钠以诱导和维持阴茎勃起时的生理反应。将硝普钠以递增浓度注射到大鼠、狗和猴子的海绵体组织中。在10只大鼠中注射的剂量分别为10^(-4)M、10^(-3)M和10^(-2)M;在5只狗和5只猴子中注射的剂量为10^(-4)M和10^(-3)M。大鼠注射的药物体积为0.05ml,狗和猴子为0.5ml。结果显示,对硝普钠注射存在剂量依赖性的勃起反应(注射10^(-3)M硝普钠后,狗的海绵体内平均压力升高102.4cm H2O,猴子为98.4cm H2O)。然而,在大鼠中仅观察到海绵体内压力有轻微升高(注射10^(-2)M硝普钠后平均升高28.4cm H2O)。狗和猴子的血压下降>15mmHg,而大鼠的血压下降则根据所研究的剂量而有所不同。硝普钠在狗和猴子中能诱导出良好的勃起,且对血压的改变最小。然而,在大鼠中给药会导致低血压。硝普钠可能不是治疗男性勃起功能障碍可接受的一氧化氮供体。

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