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血栓素A合成酶抑制剂Y-19018对大鼠新月体型抗肾小球基底膜肾炎的抗肾炎作用

Antinephritic effect of Y-19018, a thromboxane A synthetase inhibitor, on crescentic-type anti-GBM nephritis in rats.

作者信息

Suzuki Y, Tsukushi Y, Ito M, Nagamatsu T

机构信息

Department of Pharmacology, Faculty of Pharmacy, Meijo University, Nagoya, Japan.

出版信息

Jpn J Pharmacol. 1987 Oct;45(2):177-85. doi: 10.1254/jjp.45.177.

Abstract

In order to investigate the antinephritic effect of Y-19018, a thromboxane A synthetase inhibitor, on crescentic-type anti-glomerular basement membrane (anti-GBM) nephritis in rats, the present study was undertaken. Male Sprague Dawley rats were immunized with rabbit gamma-globulin in Freund's complete adjuvant following i.v. injection of anti-GBM serum. Y-19018 at a dose of 0.3 and 3.0 mg/kg was given orally to rats from the day after the injection of anti-GBM serum (day 1) to day 39. Y-19018, 3.0 mg/kg, significantly inhibited both urinary protein excretion (30.6%) on day 19 and plasma cholesterol (39.8%) on day 15. Moreover, light microscopy demonstrated that this drug at both doses remarkably prevented histological involvement of the glomeruli on day 40 in a dose-dependent manner. In the blood obtained from nephritic rats, platelet aggregation was increased. Y-19018 suppressed (48.7%) the hyperaggregability of platelets on day 40 at a high dose, although the suppression of platelet aggregation was not in a dose-dependent manner. It is concluded from these data that Y-19018 shows beneficial effects on crescentic-type anti-GBM nephritis and may exert its action partly through inhibition of glomerular TXA2.

摘要

为了研究血栓素A合成酶抑制剂Y-19018对大鼠新月体型抗肾小球基底膜(anti-GBM)肾炎的抗肾炎作用,进行了本研究。雄性Sprague Dawley大鼠在静脉注射抗GBM血清后,用弗氏完全佐剂中的兔γ球蛋白进行免疫。从注射抗GBM血清后的第二天(第1天)到第39天,以0.3和3.0mg/kg的剂量给大鼠口服Y-19018。3.0mg/kg的Y-19018在第19天显著抑制尿蛋白排泄(30.6%),在第15天显著抑制血浆胆固醇(39.8%)。此外,光学显微镜显示,两种剂量的该药物在第40天均以剂量依赖的方式显著预防了肾小球的组织学病变。在从患肾炎大鼠获得的血液中,血小板聚集增加。高剂量的Y-19018在第40天抑制了血小板的高聚集性(48.7%),尽管对血小板聚集的抑制不是剂量依赖性的。从这些数据得出结论,Y-19018对新月体型抗GBM肾炎显示出有益作用,并且可能部分通过抑制肾小球TXA2发挥其作用。

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