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硫酸鱼精蛋白对大鼠和小鼠SR 90107A/Org 31540诱导出血的拮抗作用。

Antagonism of SR 90107A/Org 31540-induced bleeding by protamine sulfate in rats and mice.

作者信息

Bernat A, Hoffmann P, Herbert J M

机构信息

Sanofi Recherche, Toulouse, France.

出版信息

Thromb Haemost. 1996 Nov;76(5):715-9.

PMID:8950779
Abstract

The neutralization by protamine sulfate of bleeding enhancement induced by the potent anti-factor Xa pentasaccharide SR 90107A/Org 31540 and by heparin has been studied in rats and mice. Bleeding, as measured by transection of the tail of anaesthetised rats or mice, was increased following the administration of heparin and very high doses of SR 90107A/Org 31540. In rats, i.v. doses of 0.6 mg/kg heparin or 15 mg/kg SR 90107A/Org 31540 were required to enhance bleeding time to approximately the same extent (5- or 7-fold increase), whereas in mice a 13-fold increase in blood loss was observed with i.v. doses of 3 mg/kg heparin or 10 mg/kg SR 90107A/Org 31540. Protamine sulfate (10 mg/kg i.v.) reduced bleeding in rats and mice induced by both compounds. It also neutralized the anti-factor Xa activity as well as the antithrombotic activity of heparin as observed in venous thrombosis models in both species. However, protamine sulfate neither affected the anti-factor Xa activity nor the antithrombotic activity of SR 90107A/Org 31540 in rats and mice. The present results suggest that protamine sulfate may be regarded as a potential antidote to neutralize bleeding side-effects in cases of SR 90107A/Org 31540 overdosing.

摘要

在大鼠和小鼠中研究了硫酸鱼精蛋白对强效抗Xa因子五糖SR 90107A/Org 31540和肝素诱导的出血增强作用的中和效果。通过切断麻醉大鼠或小鼠的尾巴来测量出血情况,给予肝素和非常高剂量的SR 90107A/Org 31540后出血增加。在大鼠中,静脉注射0.6 mg/kg肝素或15 mg/kg SR 90107A/Org 31540可使出血时间延长至大致相同的程度(增加5倍或7倍),而在小鼠中,静脉注射3 mg/kg肝素或10 mg/kg SR 90107A/Org 31540可使失血量增加13倍。硫酸鱼精蛋白(静脉注射10 mg/kg)可减少两种化合物在大鼠和小鼠中诱导的出血。在这两个物种的静脉血栓形成模型中,它还中和了肝素的抗Xa因子活性以及抗血栓活性。然而,硫酸鱼精蛋白对大鼠和小鼠中SR 90107A/Org 31540的抗Xa因子活性和抗血栓活性均无影响。目前的结果表明,在SR 90107A/Org 31540过量的情况下,硫酸鱼精蛋白可被视为一种潜在的解毒剂,用于中和出血副作用。

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