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拟交感胺诱导的大鼠纤溶活性增强部分受内源性前列腺素调节。

Sympathomimetic amine-induced potentiation of fibrinolytic activity is partly modulated by endogenous prostaglandins in the rat.

作者信息

Hussaini I M, Moore P K

机构信息

Department of Chemistry, University of Virginia, Charlottesville 22901.

出版信息

Thromb Res. 1989 Sep 1;55(5):611-7. doi: 10.1016/0049-3848(89)90393-9.

Abstract

Blood fibrinolytic activity was assessed on fibrin plates. Epinephrine and norepinephrine produced a time-dependent potentiation of fibrinolysis following intravenous injection into rats which was reduced by indomethacin (3 mg/kg, i.v.) and completely abolished by phentolamine (0.1 mg/kg, i.v.). Propranolol (0.5 mg/kg) had no effect on the fibrinolysis produced by epinephrine. The study demonstrates that endogenous prostaglandins modulate in part the fibrinolysis induced by sympathomimetic amines via activation of alpha-adrenoceptors in vivo.

摘要

在纤维蛋白平板上评估血液纤溶活性。给大鼠静脉注射肾上腺素和去甲肾上腺素后,纤溶作用呈时间依赖性增强,吲哚美辛(3毫克/千克,静脉注射)可降低这种增强作用,酚妥拉明(0.1毫克/千克,静脉注射)则可完全消除这种增强作用。普萘洛尔(0.5毫克/千克)对肾上腺素引起的纤溶作用没有影响。该研究表明,内源性前列腺素在体内通过激活α-肾上腺素能受体部分调节拟交感胺诱导的纤溶作用。

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