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某些新型前列腺素合成酶抑制剂对实验动物内毒素诱导的死亡率及生化变化的影响

Effect of some new prostaglandin synthetase inhibitors on the endotoxin induced mortality and biochemical changes in experimental animals.

作者信息

Tariq M

机构信息

College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Res Commun Chem Pathol Pharmacol. 1988 Apr;60(1):19-25.

PMID:3132734
Abstract

The protective effect of some novel nonsteroidal anti-inflammatory agents has been studied on the endotoxin (lipopolysaccharide B) shock induced mortality in mice and biochemical changes in rats. All the three compounds included in this report, namely isoxicam, fentiazac and ketoprofen have been found to produce significant protection against the endotoxin mortality in mice. Isoxicam and fentiazac have been found effective in antagonizing some of the biochemical changes induced by endotoxin in rats. On the other hand isoxicam and ketoprofen exacerbated the increase in serum aminotransferases induced by endotoxin. It is suggested that mechanisms other than the prostaglandin synthetase inhibition may be involved in the protective effect of these drugs.

摘要

研究了一些新型非甾体抗炎药对小鼠内毒素(脂多糖B)休克诱导的死亡率以及大鼠生化变化的保护作用。本报告中包含的三种化合物,即异恶酰胺、芬替酸和酮洛芬,均已被发现对小鼠内毒素致死率具有显著的保护作用。已发现异恶酰胺和芬替酸可有效对抗内毒素在大鼠中诱导的一些生化变化。另一方面,异恶酰胺和酮洛芬加剧了内毒素诱导的血清转氨酶升高。提示这些药物的保护作用可能涉及除抑制前列腺素合成酶以外的其他机制。

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