Role of cytochrome P-450 in endogenous antipyresis

1  Department of Physiology, Medical College of Georgia, Augusta, Georgia 30912; and 2  Department of Medicine, University of New Mexico, Albuquerque, New Mexico 87131 In previous reports, we (15, 18) and others (29) demonstrated data showing that various inhibitors of cytochrome P -450/epoxygenase...

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Veröffentlicht in:American journal of physiology. Regulatory, integrative and comparative physiology integrative and comparative physiology, 2000-08, Vol.279 (2), p.455-R460
Hauptverfasser: Kozak, Wieslaw, Kluger, Matthew J, Kozak, Anna, Wachulec, Maciej, Dokladny, Karol
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container_issue 2
container_start_page 455
container_title American journal of physiology. Regulatory, integrative and comparative physiology
container_volume 279
creator Kozak, Wieslaw
Kluger, Matthew J
Kozak, Anna
Wachulec, Maciej
Dokladny, Karol
description 1  Department of Physiology, Medical College of Georgia, Augusta, Georgia 30912; and 2  Department of Medicine, University of New Mexico, Albuquerque, New Mexico 87131 In previous reports, we (15, 18) and others (29) demonstrated data showing that various inhibitors of cytochrome P -450/epoxygenase augment fever in rats and mice, indicating that the enzyme may be involved in endogenous antipyresis. The aim of this study was to further test the hypothesis that the P -450-dependent epoxygenase pathway of arachidonic acid is part of the homeostatic system to control the height of fever. Sprague-Dawley rats were implanted with biotelemeters to monitor body temperature. Fever was induced by intraperitoneal injection of lipopolysaccharide (LPS; 80 µg/kg). We demonstrate that intraperitoneal administration of P -450 inducers (bezafibrate and dehydroepiandrosterone, 10 and 100 mg/kg) before LPS reduced fever in rats in a dose-dependent manner. In complementary experiments, rats were implanted with brain cannulas in addition to the biotelemeters. Various isomers of epoxyeicosanoids were administered into the lateral ventricle at doses of 0.01 to 10   µg/rat to test their influence on LPS-induced fever in rats. Four of five isomers were antipyretic in a dose-dependent manner. The most potent antipyretic isomers were 11,12-epoxyeicosatrienoic acid (EET) followed by 14,15-EET, 8,9-EET, and 12(R) hydroxyeicosatetraenoic acid. These data support the hypothesis that the cytochrome P -450/epoxygenase pathway of arachidonate metabolism is part of the endogenous antipyretic system. biotelemetry; body temperature; lipopolysaccharide; brain stereotaxic surgery; cerebral lateral ventricle; fever mechanism; epoxygenase; bezafibrate; dehydroepiandrosterone; epoxyeicosanoids; epoxyeicosatrienoic acids; hydroxyeicosatetraenoic acids
doi_str_mv 10.1152/ajpregu.2000.279.2.R455
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subjects Analgesics, Non-Narcotic - pharmacology
Animals
Cytochrome P-450 Enzyme System - pharmacology
Cytochrome P-450 Enzyme System - physiology
Eicosanoids - pharmacology
Fever - chemically induced
Fever - physiopathology
Injections, Intraventricular
Lipopolysaccharides
Male
Protein Isoforms - pharmacology
Rats
Rats, Sprague-Dawley
title Role of cytochrome P-450 in endogenous antipyresis
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