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连苯三酚和亚甲蓝对灌注大鼠肠系膜动脉的舒张机制

Mechanisms of relaxation by pyrogallol and methylthioninium chloride in perfused rat mesenteric artery.

作者信息

Li Y J, Duckles S P

机构信息

Department of Pharmacology, College of Medicine, University of California, Irvine 92717.

出版信息

Zhongguo Yao Li Xue Bao. 1994 Mar;15(2):142-7.

PMID:8010109
Abstract

In perfused rat mesenteric arteries without endothelium, pyrogallol (Pyr) or methylthioninium chloride (methylene blue, Met) produced a concentration-dependent relaxation. Superoxide dismutase abolished inhibition by Pyr, but not Met, of vasoconstrictor responses to transmural nerve stimulation (TNS). Neither catalase nor deferoxamine had any effect on vasodilator responses to Pyr or Met. Vasodilator responses to Pyr were unaltered by N omega-nitro-L-arginine methyl ester (L-NAME), indomethacin, or capsaicin. Similarly, the relaxing effect of Met was unaffected by indomethacin or capsaicin. These findings suggest that vasodilator responses to Pyr may be due to endothelial-independent generation of superoxide anion. In contrast the relaxation produced by Met appears to be due to a direct action on vascular smooth muscle independent of superoxide anion generation.

摘要

在无内皮的灌注大鼠肠系膜动脉中,连苯三酚(Pyr)或亚甲蓝(Met)可产生浓度依赖性舒张作用。超氧化物歧化酶消除了Pyr对跨壁神经刺激(TNS)引起的血管收缩反应的抑制作用,但对Met无此作用。过氧化氢酶和去铁胺对Pyr或Met引起的血管舒张反应均无影响。Pyr引起的血管舒张反应不受Nω-硝基-L-精氨酸甲酯(L-NAME)、吲哚美辛或辣椒素的影响。同样,Met的舒张作用也不受吲哚美辛或辣椒素的影响。这些发现表明,Pyr引起的血管舒张反应可能是由于超氧阴离子的非内皮依赖性生成。相比之下,Met产生的舒张作用似乎是由于对血管平滑肌的直接作用,与超氧阴离子的生成无关。

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