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华法林与非甾体抗炎药(NSAIDs)在大鼠体内的相互作用。

Interaction between warfarin and nonsteroidal anti-inflammatory drugs (NSAIDs) in rats.

作者信息

Sancilio L F, Taylor M A, Mathur P P, Crowe J T

出版信息

Life Sci. 1985 Mar 18;36(11):1041-50. doi: 10.1016/0024-3205(85)90489-8.

Abstract

In fed rats, the following NSAIDs were administered orally 24 hr before or 18 hr after the intraperitoneal administration of 1.34 mg/kg warfarin: phenylbutazone, 150 mg/kg; diflunisal, 75 mg/kg; ibuprofen, 150 mg/kg; acetylsalicylic acid, 300 mg/kg; indomethacin, 8 mg/kg; tolmetin sodium, 50 mg/kg; ketoprofen, 8 mg/kg; and amfenac sodium, 8 mg/kg. The elevation of the 24-hr prothrombin time was indicative of the effect of the warfarin. Warfarin-treated fasted rats showed a significantly higher prothrombin time than warfarin-treated fed rats. Interaction with phenylbutazone and warfarin occurred in fed and not in fasted rats when administered 18 hr after administration of the warfarin. At the 24-hr pretreatment time, only phenylbutazone significantly reduced the elevated prothrombin time. With the exception of amfenac sodium, all the NSAIDs significantly enhanced the elevated prothrombin time when administered 18 hr after warfarin. Their decreasing order of activity in enhancing the elevated prothrombin time was phenylbutazone, diflunisal, acetylsalicylic acid, ibuprofen, indomethacin, tolmetin sodium, and ketoprofen. The results indicate that the rat is more sensitive than the human to the interaction between warfarin and NSAIDs.

摘要

在喂食状态的大鼠中,于腹腔注射1.34mg/kg华法林前24小时或注射后18小时口服给予以下非甾体抗炎药:保泰松,150mg/kg;二氟尼柳,75mg/kg;布洛芬,150mg/kg;乙酰水杨酸,300mg/kg;吲哚美辛,8mg/kg;托美丁钠,50mg/kg;酮洛芬,8mg/kg;以及氨芬酸钠,8mg/kg。24小时凝血酶原时间的升高表明了华法林的作用效果。经华法林处理的禁食大鼠的凝血酶原时间显著高于经华法林处理的喂食大鼠。当在华法林给药后18小时给药时,保泰松与华法林之间的相互作用在喂食大鼠中出现,而在禁食大鼠中未出现。在24小时预处理时,只有保泰松显著降低了升高的凝血酶原时间。除氨芬酸钠外,所有非甾体抗炎药在华法林给药后18小时给药时均显著延长了升高的凝血酶原时间。它们在延长升高的凝血酶原时间方面的活性递减顺序为保泰松、二氟尼柳、乙酰水杨酸、布洛芬、吲哚美辛、托美丁钠和酮洛芬。结果表明,大鼠对华法林与非甾体抗炎药之间的相互作用比人类更敏感。

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