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血栓素合成抑制剂 - 受体拮抗剂组合R - 68070在小鼠创伤性休克中的保护作用

Protective effects of a combination thromboxane synthesis inhibitor-receptor antagonist, R-68070, during murine traumatic shock.

作者信息

Aoki N, Johnson G, Siegfried M R, Lefer A M

机构信息

Department of Physiology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107.

出版信息

Eicosanoids. 1989;2(3):169-74.

PMID:2534278
Abstract

The effects of R-68070 were studied in a well-characterized model of drum-induced traumatic shock in rats. R-68070 is a combination thromboxane A2 (TxA2) synthetase inhibitor-TxA2 receptor antagonist. Pentobarbital-anesthetized (50 mg/kg) rats subjected to Noble-Collip drum trauma developed a lethal circulatory shock state characterized by a marked decrease in mean arterial blood pressure (MABP) to about 75 mmHg, resulting in a survival time of 1.58 +/- 0.18 h. This compares with MABP of 120 +/- 4 mmHg 5 h after anesthetization in rats subjected to a sham traumatic shock protocol. Administration of R-68070 (1.5 mg/kg) significantly attenuated the plasma accumulation of the lysosomal protease, cathepsin D (p less than 0.05), as well as free amino-nitrogen concentration (p less than 0.05) and myocardial depressant factor activity (p less than 0.02). Additionally, R-68070 significantly prolonged survival time to 2.85 +/- 0.48 h (p less than 0.015) compared with traumatized rats given only the vehicle. These results suggest that TxA2 may be an important mediator in traumatic shock, and that R-68070 may prove to be a useful therapeutic agent in this situation if given early in the course of the shock state.

摘要

在一个特征明确的大鼠鼓击诱导创伤性休克模型中研究了R-68070的作用。R-68070是一种血栓素A2(TxA2)合成酶抑制剂-TxA2受体拮抗剂的组合。经戊巴比妥麻醉(50mg/kg)的大鼠遭受诺布尔-科利普鼓击创伤后会出现致命的循环休克状态,其特征为平均动脉血压(MABP)显著下降至约75mmHg,导致存活时间为1.58±0.18小时。相比之下,在接受假创伤性休克方案的大鼠中,麻醉后5小时MABP为120±4mmHg。给予R-68070(1.5mg/kg)可显著减轻溶酶体蛋白酶组织蛋白酶D的血浆蓄积(p<0.05),以及游离氨基氮浓度(p<0.05)和心肌抑制因子活性(p<0.02)。此外,与仅给予赋形剂的创伤大鼠相比,R-68070显著延长了存活时间至2.85±0.48小时(p<0.015)。这些结果表明TxA2可能是创伤性休克中的一种重要介质,并且如果在休克状态过程中早期给予,R-68070可能被证明是一种有用的治疗药物。

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