首页> 美国卫生研究院文献>Asian Journal of Andrology >Effects of Ginkgo biloba extracts with mirodenafil on the relaxation of corpus cavernosal smooth muscle and the potassium channel activity of corporal smooth muscle cells
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Effects of Ginkgo biloba extracts with mirodenafil on the relaxation of corpus cavernosal smooth muscle and the potassium channel activity of corporal smooth muscle cells

机译:银杏叶提取物与美罗那非对海绵体海绵体平滑肌松弛和体质平滑肌细胞钾通道活性的影响

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摘要

In this study, we investigated the effects of a combination of Ginkgo biloba extracts (GBE) and phosphodiesterase type 5 (PDE-5) inhibitors on the muscular tone of the corpus cavernosum and potassium channel activity of corporal smooth muscle cells. Strips of corpus cavernosum from male New Zealand white rabbits were mounted in organ baths for isometric tension studies. After contraction with 1×10−5 mol l−1 norepinephrine, GBE (0.01–1 mg ml−1) and mirodenafil (0.01–100 nmol l−1) were added together into the organ bath. In electrophysiological studies, whole-cell currents were recorded by the conventional patch-clamp technique in cultured smooth muscle cells of the human corpus cavernosum. The corpus cavernosum was relaxed in response to GBE in a dose-dependent manner (from 0.64%±8.35% at 0.01 mg ml−1 to 52.28%±11.42% at 1 mg ml−1). After pre-treatment with 0.03 mg ml−1 of GBE, the relaxant effects of mirodenafil were increased at all concentrations. After tetraethylammonium (TEA) (1 mmol l−1) administration, the increased effects were inhibited (P<0.01). Extracellular administration of GBE increased the whole-cell K+ outward currents in a dose-dependent fashion. The increase of the outward current was inhibited by 1 mmol l−1 TEA. These results suggest that GBE could increase the relaxant potency of mirodenafil even at a minimally effective dose. The K+ flow through potassium channels might be one of the mechanisms involved in this synergistic relaxation.
机译:在这项研究中,我们调查了银杏叶提取物(GBE)和5型磷酸二酯酶(PDE-5)抑制剂的组合对海绵体肌张力和体液平滑肌细胞钾通道活性的影响。将来自雄性新西兰白兔的海绵体条安装在器官浴中用于等轴测张力研究。用1×10 −5 mol ls −1 去甲肾上腺素收缩后,GBE(0.01–1 mg ml −1 )和米洛那非(0.01–1将100 nmol l -1 )一起添加到器官浴中。在电生理研究中,通过常规膜片钳技术在人海绵体的平滑肌细胞中记录了全细胞电流。海绵体对GBE的反应呈剂量依赖性(从0.01mg ml -1 的0.64%±8.35%降至1mg ml -1的52.28%±11.42% )。用0.03 mg ml -1 的GBE预处理后,米罗地那非的放松作用在所有浓度下均增加。施用四乙铵(TEA)(1 mmol l -1 )后,抑制作用增加(P <0.01)。 GBE的细胞外给药以剂量依赖性方式增加了全细胞的K + 外向电流。 1 mmol l -1 TEA抑制了向外电流的增加。这些结果表明,即使在最小有效剂量下,GBE仍可增加美洛那非的舒张效力。通过钾通道的K + 可能是这种协同弛豫的机制之一。

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