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首页> 外文期刊>American Journal of Physiology >cGMP-independent mechanism of airway smooth muscle relaxation induced by S-nitrosoglutathione.
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cGMP-independent mechanism of airway smooth muscle relaxation induced by S-nitrosoglutathione.

机译:S-亚硝基谷胱甘肽诱导的cGMP依赖性气道平滑肌松弛机制。

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摘要

This study tested the hypothesis that the NO donor S-nitrosoglutathione (GSNO) relaxes canine tracheal smooth muscle (CTSM) in part by a cGMP-independent process that involves reversible oxidation of intracellular thiols. GSNO caused a concentration-dependent relaxation in ACh-contracted strips (EC50 approximately 1.2 microM) accompanied by a concentration-dependent increase in cytosolic cGMP concentration ([cGMP]i). The soluble guanylate cyclase inhibitor methylene blue prevented the increase in [cGMP]i induced by 1 and 10 microM GSNO, but isometric force decreased by 10 +/- 4 and 55 +/- 3%, respectively. After recovery of [cGMP]i to baseline, GSNO-induced relaxation persisted during continuous ACh stimulation. Dithiothreitol caused a rapid recovery of isometric force to values similar to those obtained with ACh alone in these strips. We conclude that GSNO relaxes CTSM contracted by ACh in part by oxidation of intracellular protein thiols.
机译:这项研究检验了NO供体S-亚硝基谷胱甘肽(GSNO)可以部分通过cGMP独立过程(涉及细胞内硫醇可逆氧化)使犬气管平滑肌(CTSM)松弛的假设。 GSNO导致ACh收缩条带的浓度依赖性松弛(EC50约为1.2 microM),同时胞质cGMP浓度([cGMP] i)浓度依赖性增加。可溶性鸟苷酸环化酶抑制剂亚甲基蓝阻止了1和10 microM GSNO诱导的[cGMP] i的增加,但等轴测力分别降低了10 +/- 4和55 +/- 3%。 [cGMP] i恢复到基线后,在连续的ACh刺激过程中,GSNO诱导的松弛持续存在。二硫苏糖醇使等轴测力迅速恢复到类似于在这些试纸条上单独使用ACh所获得的值。我们得出结论,GSNO放松了ACh收缩的CTSM,部分原因是细胞内蛋白硫醇的氧化。

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