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花生四烯酸代谢旁路抑制剂对小鼠发热有不同影响。

Inhibitors of alternative pathways of arachidonate metabolism differentially affect fever in mice.

作者信息

Kozak W, Archuleta I, Mayfield K P, Kozak A, Rudolph K, Kluger M J

机构信息

Lovelace Respiratory Research Institute, Inhalation Toxicology Laboratory, Albuquerque, New Mexico 87185, USA.

出版信息

Am J Physiol. 1998 Oct;275(4):R1031-40. doi: 10.1152/ajpregu.1998.275.4.R1031.

Abstract

Inhibitors of cyclooxygenases prevent fever. The purpose of this study was to test the hypothesis that selective and dual inhibitors of the other enzyme systems of arachidonic acid oxygenation (i.e., lipoxygenase and epoxygenase) affect the time course or magnitude of fever in mice. Swiss Webster mice kept at 30 degreesC ambient temperature were implanted with biotelemeters to monitor body temperature. Fever was induced by intraperitoneal injection of lipopolysaccharide at doses from 10 micrograms/kg to 2.5 mg/kg. Phenidone (20-30 mg/kg ip), a dual lipoxygenase and cyclooxygenase inhibitor, prevented fever in these mice, but esculetin (1-10 mg/kg ip), a selective inhibitor of lipoxygenases, did not affect fever. Intramuscular injection of nordihydroguaiaretic acid (10-20 mg/kg), a dual lipoxygenase and epoxygenase inhibitor, as well as SKF-525A (5 mg/kg ip) and clotrimazole (20 mg/kg im), inhibitors of the cytochrome P-450/epoxygenase pathway, augmented fever in mice. Indomethacin (5 mg/kg ip), an inhibitor of cyclooxygenase, suppressed the exacerbation of fever due to clotrimazole, suggesting that the epoxygenase inhibitor-induced potentiation of fever in mice is a prostaglandin-mediated effect. From this study, we hypothesize that the cytochrome P-450/epoxygenase branch of the arachidonate cascade is involved in antipyresis and in controlling the upper limit of fever.

摘要

环氧化酶抑制剂可预防发热。本研究的目的是检验以下假设:花生四烯酸氧化的其他酶系统(即脂氧合酶和环氧合酶)的选择性抑制剂和双重抑制剂会影响小鼠发热的时间进程或程度。将饲养在30℃环境温度下的瑞士韦伯斯特小鼠植入生物遥测仪以监测体温。通过腹腔注射剂量为10微克/千克至2.5毫克/千克的脂多糖诱导发热。双脂氧合酶和环氧化酶抑制剂非那吡啶(20 - 30毫克/千克腹腔注射)可预防这些小鼠发热,但脂氧合酶的选择性抑制剂七叶亭(1 - 10毫克/千克腹腔注射)对发热无影响。肌肉注射双脂氧合酶和环氧合酶抑制剂去甲二氢愈创木酸(10 - 20毫克/千克)以及细胞色素P - 450/环氧合酶途径的抑制剂SKF - 525A(5毫克/千克腹腔注射)和克霉唑(20毫克/千克肌肉注射)会使小鼠发热加剧。环氧化酶抑制剂吲哚美辛(5毫克/千克腹腔注射)可抑制由克霉唑引起的发热加剧,这表明环氧合酶抑制剂诱导的小鼠发热增强是一种前列腺素介导的效应。基于本研究,我们推测花生四烯酸级联反应的细胞色素P - 450/环氧合酶分支参与了退热作用并控制发热的上限。

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