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血栓素A2合成酶抑制剂Y-20811对麻醉犬实验性诱导冠状动脉血栓形成的影响。

Effects of Y-20811, a thromboxane A2 synthetase inhibitor, on experimentally induced coronary thrombosis in anesthetized dogs.

作者信息

Matsumoto Y, Ochi H, Aihara K, Inui J, Ikegami K

机构信息

Research Laboratories, Tokyo Yoshitomi Pharmaceutical Industries, Ltd., Saitama, Japan.

出版信息

Eur J Pharmacol. 1992 Mar 24;213(2):167-70. doi: 10.1016/0014-2999(92)90677-v.

Abstract

The effects of Y-20811, a selective inhibitor of thromboxane A2 (TXA2) synthetase, on blood flow and local levels of immunoreactive thromboxane B2 (i-TXB2) and 6-keto prostaglandin F1 alpha (i-6-keto PGF1 alpha) in the coronary artery were investigated in the canine model of coronary thrombosis. Thrombosis was induced by applying an electric current to the intraluminal surface of the coronary artery. The plasma levels of i-TXB2 and i-6-keto PGF1 alpha were measured distal to the electrode. In the control group, coronary blood flow decreased and finally stopped 207 +/- 53 min (mean +/- S.E.M., n = 5) after the start of current application. The level of i-TXB2 rose before the coronary occlusion. Coronary blood flow did not change significantly in the Y-20811-treated group (1 mg/kg i.v.). The level of i-TXB2 decreased and remained significantly lower than that in the control group. The level of i-6-keto PGF1 alpha tended to increase slightly in the Y-20811-treated, but not in the control group. The weight of the thrombus in the Y-20811-treated group was significantly less than that in the control group (P less than 0.01). These results suggest that Y-20811 prevents coronary thrombosis by the inhibition of TXA2 production around the electrically injured lumen of the coronary artery.

摘要

在犬冠状动脉血栓形成模型中,研究了血栓素A2(TXA2)合成酶的选择性抑制剂Y-20811对冠状动脉血流以及免疫反应性血栓素B2(i-TXB2)和6-酮前列腺素F1α(i-6-酮PGF1α)局部水平的影响。通过对冠状动脉腔内表面施加电流诱导血栓形成。在电极远端测量i-TXB2和i-6-酮PGF1α的血浆水平。在对照组中,施加电流后207±53分钟(平均值±标准误,n = 5)冠状动脉血流减少并最终停止。冠状动脉闭塞前i-TXB2水平升高。在Y-20811治疗组(静脉注射1mg/kg)中冠状动脉血流无显著变化。i-TXB2水平降低且仍显著低于对照组。在Y-20811治疗组中i-6-酮PGF1α水平略有升高趋势,但在对照组中无此现象。Y-20811治疗组血栓重量显著低于对照组(P<0.01)。这些结果表明,Y-20811通过抑制冠状动脉电损伤腔周围的TXA2产生来预防冠状动脉血栓形成。

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