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内皮素和铃蟾毒素 S6b 具有相似的血管收缩作用和突触后介导机制。

Endothelin and sarafotoxin S6b have similar vasoconstrictor effects and postsynaptically mediated mechanisms.

作者信息

Han S P, Knuepfer M M, Trapani A J, Fok K F, Westfall T C

机构信息

Department of Pharmacology, Saint Louis University School of Medicine, MO 63104.

出版信息

Eur J Pharmacol. 1990 Feb 20;177(1-2):29-34. doi: 10.1016/0014-2999(90)90546-i.

Abstract

In the isolated perfused mesenteric vascular bed, porcine endothelin (ET) and sarafotoxin S6b produced direct vasoconstriction and potentiated nerve stimulation-induced vasoconstriction. ET also enhanced the vasoconstrictor response to exogenous norepinephrine (NE). Basal or stimulated endogenous NE release was not affected either by ET or sarafotoxin S6b. Qualitatively similar responses to ET and sarafotoxin S6b were always observed, although, in many cases, the response to ET was greater and longer lasting than to sarafotoxin S6b. These results indicate that vasoconstrictor responses to ET or sarafotoxin S6b are mediated primarily by postsynaptic mechanisms. No initial vasodilator response to ET or sarafotoxin S6b was observed in this mesenteric vascular preparation.

摘要

在离体灌注的肠系膜血管床中,猪内皮素(ET)和蛙皮毒素S6b可引起直接血管收缩,并增强神经刺激诱导的血管收缩。ET还增强了对外源性去甲肾上腺素(NE)的血管收缩反应。ET或蛙皮毒素S6b对基础或刺激引起的内源性NE释放均无影响。尽管在许多情况下,对ET的反应比对蛙皮毒素S6b的反应更大且持续时间更长,但对ET和蛙皮毒素S6b的定性相似反应始终可见。这些结果表明,对ET或蛙皮毒素S6b的血管收缩反应主要由突触后机制介导。在这种肠系膜血管制剂中未观察到对ET或蛙皮毒素S6b的初始血管舒张反应。

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