首页> 外文期刊>Naunyn-Schmiedeberg's Archives of Pharmacology >Involvement of cyclic GMP and potassium channels in relaxation evoked by the nitric oxide donor, diethylamine NONOate, in the rat small isolated mesenteric artery
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Involvement of cyclic GMP and potassium channels in relaxation evoked by the nitric oxide donor, diethylamine NONOate, in the rat small isolated mesenteric artery

机译:一氧化氮供体二乙胺NONOate在大鼠小肠系膜动脉中引起的环GMP和钾通道参与放松

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摘要

The relative functional importance of potassium channels and cGMP-dependent pathways in the relaxation of vascular smooth muscle to the novel nitric oxide donor, diethylamine NONOate (DEA NONOate), was investigated in a resistance artery. The contribution from cGMP-dependent signalling pathways was examined by exposing arteries to 1H-[1,2,4]oxadiazolo[4,3-a]quinoxalin-1-one (ODQ), a selective inhibitor of soluble guanylyl cyclase, while the contribution through potassium channels was assessed with different sub-type-selective potassium channel blockers.
机译:在阻力动脉中研究了钾通道和cGMP依赖性途径在血管平滑肌向新型一氧化氮供体NONOate(DEA NONOate)舒张中的相对功能重要性。通过将动脉暴露于1H- [1,2,4] oxadiazolo [4,3-a] quinoxalin-1-one(ODQ)(一种可溶性鸟苷酸环化酶的选择性抑制剂)来检查cGMP依赖性信号通路的作用。通过不同的亚型选择性钾通道阻滞剂评估了钾通道的贡献。

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