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维拉帕米、硝苯地平和硝酸甘油引起的外周血管舒张对血浆前列腺素和血栓素浓度的影响。

Effects of peripheral vasodilation caused by verapamil, nifedipine, and nitroglycerin on plasma prostaglandins and thromboxane concentrations.

作者信息

Kai I, Ogawa K, Ito T

出版信息

Jpn Heart J. 1982 Nov;23(6):941-9. doi: 10.1536/ihj.23.941.

Abstract

We investigated the vasodilating effects of verapamil, nifedipine, and nitroglycerin in relation to plasma levels of 6-keto-prostaglandin (PG)-F1 alpha, PG E1, PG F2 alpha, and thromboxane (TX) B2 in dogs. Verapamil, nifedipine, and nitroglycerin decreased peripheral vascular resistance from 1.00 +/- 0.07 mmHg/ml/min (mean +/- SE) to 0.83 +/- 0.05, from 0.99 +/- 0.06 to 0.80 +/- 0.05, and from 1.03 +/- 0.04 to 0.91 +/- 0.04, respectively. However, peripheral blood flow did not change significantly. Administration of verapamil significantly increased plasma levels of 6-keto-PG F1 alpha, PG E1, and PG F2 alpha from 150 +/- 31 pg/ml to 350 +/- 98, from 56 +/- 34 to 87 +/- 33, and from 127 +/- 35 to 238 +/- 61, respectively, while neither nifedipine nor nitroglycerin had any effect on plasma 6-keto-PG F1 alpha, PG E1, and PG F2 alpha. Indomethacin pretreatment reduced the effects of verapamil on peripheral vascular resistance and plasma PG concentration. None of these drugs caused a significant change in the plasma TX B2 level. The results suggest that the vasodilating action of verapamil was mediated in part by the prostaglandin system.

摘要

我们研究了维拉帕米、硝苯地平和硝酸甘油在犬体内的血管舒张作用与血浆中6-酮-前列腺素(PG)-F1α、PGE1、PGF2α和血栓素(TX)B2水平的关系。维拉帕米、硝苯地平和硝酸甘油分别使外周血管阻力从1.00±0.07mmHg/ml/min(平均值±标准误)降至0.83±0.05、从0.99±0.06降至0.80±0.05、从1.03±0.04降至0.91±0.04。然而,外周血流量无显著变化。给予维拉帕米后,血浆中6-酮-PGF1α、PGE1和PGF2α水平显著升高,分别从150±31pg/ml升至350±98、从56±34升至87±33、从127±35升至238±61,而硝苯地平和硝酸甘油对血浆6-酮-PGF1α、PGE1和PGF2α均无影响。吲哚美辛预处理可降低维拉帕米对外周血管阻力和血浆PG浓度的影响。这些药物均未引起血浆TX B2水平的显著变化。结果表明,维拉帕米的血管舒张作用部分是由前列腺素系统介导的。

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