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L-arginine-induced relaxation of the rat isolated penile bulb.

机译:L-精氨酸诱导的大鼠离体阴茎球松弛。

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摘要

The effects of L-arginine, the precursor in the synthesis of nitric oxide (NO), were investigated in the penile bulb isolated from saline (control) or lipopolysaccharide (20 mg/kg, i.p.)-treated rats. Four consecutive concentration-response curves for L-arginine were made at hourly intervals with the penile bulb. L-arginine (10(7)-10(-3) M) elicited a concentration- and time-dependent relaxation response in the control group. The NO synthase (NOS) inhibitors, N(G)-methyl-L-arginine (L-NMMA) and aminoguanidine, guanylate cyclase inhibitor, 1-H-[1,2,4]oxadiazolo-[4,3-a]quinoxalin-1-one (ODQ) and protein synthesis inhibitor, cycloheximide, inhibited L-arginine-induced relaxation. In the lipopolysaccharide-group, L-arginine produced a pronounced non-time-dependent relaxation at the first concentration-response curve, which was not different from the fourth response of the control group. This response was also inhibited by aminoguanidine. These results show that L-arginine induced NO-mediated relaxation and suggest the presence of a biochemical pathway converting L-arginine to NO, which is probably an inducible type in the penile bulb.
机译:在分离自盐水(对照)或脂多糖(20 mg / kg,腹膜内)的大鼠的阴茎鳞茎中研究了L-精氨酸(一氧化氮(NO)合成中的前体)的作用。每小时用阴茎鳞茎绘制L-精氨酸的四个连续浓度响应曲线。 L-精氨酸(10(7)-10(-3)M)在对照组中引起浓度和时间依赖性的松弛反应。 NO合酶(NOS)抑制剂N(G)-甲基-L-精氨酸(L-NMMA)和氨基胍,鸟苷酸环化酶抑制剂1-H- [1,2,4]草二唑-[4,3-a]喹喔啉-1-酮(ODQ)和蛋白质合成抑制剂环己酰亚胺抑制L-精氨酸诱导的松弛。在脂多糖组中,L-精氨酸在第一浓度-响应曲线上产生了明显的非时间依赖性松弛,这与对照组的第四响应没有区别。该反应也被氨基胍抑制。这些结果表明,L-精氨酸可诱导NO介导的舒张,提示存在将L-精氨酸转化为NO的生化途径,这可能是阴茎鳞茎中的一种诱导型。

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