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血管舒张剂对兔主动脉中14C-去甲肾上腺素代谢的抑制作用。

Reduction of 14C-norepinephrine metabolism in rabbit aorta by vasodilators.

作者信息

Williams P B, Hudgins P M

出版信息

Blood Vessels. 1976;13(1-2):48-57. doi: 10.1159/000158078.

Abstract

In the present study, both of the major enzymes, monoamine oxidase and catechol-o-methyltransferase, involved in the degradation of norepinephrine were examined indirectly in segments of rabbit aorta by exposure of tissues to 14C-norepinephrine and subsequent isolation of metabolites from homogenates by chromatographic techniques. Segments of aorta were preincubated with vasodilators to examine their influence on accumulation and metabolism of 14C-norepinephrine. The accumulation of labeled norepinephrine by aortae was enhanced after preincubation with hydrochlorothiazide or diazoxide, and reduced after preincubation with sodium nitroprusside or nitroglycerin. However, the fraction of accumulated 14C-norepinephrine which was degraded was significantly reduced after exposure to all four vasodilators. These results suggest that a decrease in degradation of norepinephrine in vascular smooth muscle can be observed (1) in vitro and (2) fairly rapidly after exposure to vasodilators.

摘要

在本研究中,通过将组织暴露于14C - 去甲肾上腺素,随后用色谱技术从匀浆中分离代谢产物,间接检测了家兔主动脉段中参与去甲肾上腺素降解的两种主要酶,即单胺氧化酶和儿茶酚 - O - 甲基转移酶。主动脉段预先用血管舒张剂孵育,以检测它们对14C - 去甲肾上腺素积累和代谢的影响。用氢氯噻嗪或二氮嗪预先孵育后,主动脉对标记去甲肾上腺素的积累增强,而用硝普钠或硝酸甘油预先孵育后则降低。然而,暴露于所有四种血管舒张剂后,积累的14C - 去甲肾上腺素被降解的部分显著减少。这些结果表明,(1)在体外和(2)暴露于血管舒张剂后相当迅速地,可以观察到血管平滑肌中去甲肾上腺素降解的减少。

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