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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container_title | American journal of physiology. Regulatory, integrative and comparative physiology |
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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 |
format | Article |
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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</description><identifier>ISSN: 0363-6119</identifier><identifier>EISSN: 1522-1490</identifier><identifier>DOI: 10.1152/ajpregu.2000.279.2.R455</identifier><identifier>PMID: 10938232</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>American journal of physiology. Regulatory, integrative and comparative physiology, 2000-08, Vol.279 (2), p.455-R460</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c397t-6e148f0b1d378cf8cade87da3ba828acb3f33cf990f6dd94259fea01105b81d53</citedby><cites>FETCH-LOGICAL-c397t-6e148f0b1d378cf8cade87da3ba828acb3f33cf990f6dd94259fea01105b81d53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3037,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10938232$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kozak, Wieslaw</creatorcontrib><creatorcontrib>Kluger, Matthew J</creatorcontrib><creatorcontrib>Kozak, Anna</creatorcontrib><creatorcontrib>Wachulec, Maciej</creatorcontrib><creatorcontrib>Dokladny, Karol</creatorcontrib><title>Role of cytochrome P-450 in endogenous antipyresis</title><title>American journal of physiology. Regulatory, integrative and comparative physiology</title><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><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</description><subject>Analgesics, Non-Narcotic - pharmacology</subject><subject>Animals</subject><subject>Cytochrome P-450 Enzyme System - pharmacology</subject><subject>Cytochrome P-450 Enzyme System - physiology</subject><subject>Eicosanoids - pharmacology</subject><subject>Fever - chemically induced</subject><subject>Fever - physiopathology</subject><subject>Injections, Intraventricular</subject><subject>Lipopolysaccharides</subject><subject>Male</subject><subject>Protein Isoforms - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0363-6119</issn><issn>1522-1490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kMtOwzAQRS0EoqXwC5AVuwS_0sRLVFFAqgSqytpy7HGbKo2DnQjy96RqEd2wmsWce2d0ELojOCEkpQ9q23hYdwnFGCc0EwlNljxNz9B42NKYcIHP0RizKYunhIgRugphO7CccXaJRgQLllNGx4guXQWRs5HuW6c33u0geo95iqOyjqA2bg2160Kk6rZseg-hDNfowqoqwM1xTtDH_Gk1e4kXb8-vs8dFrJnI2ngKhOcWF8SwLNc218pAnhnFCpXTXOmCWca0FQLbqTGC01RYUJgQnBY5MSmboPtDb-PdZwehlbsyaKgqVcPwksxIxiklfACzA6i9C8GDlY0vd8r3kmC51yWPuuRelxx0SSr3uobk7fFEV-zAnOQOfgYgPgCbcr35Kj3IZtOH0lVu3f-1nhaK__l5V1Ur-G5_g3852RjLfgCNf41c</recordid><startdate>20000801</startdate><enddate>20000801</enddate><creator>Kozak, Wieslaw</creator><creator>Kluger, Matthew J</creator><creator>Kozak, Anna</creator><creator>Wachulec, Maciej</creator><creator>Dokladny, Karol</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20000801</creationdate><title>Role of cytochrome P-450 in endogenous antipyresis</title><author>Kozak, Wieslaw ; Kluger, Matthew J ; Kozak, Anna ; Wachulec, Maciej ; Dokladny, Karol</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c397t-6e148f0b1d378cf8cade87da3ba828acb3f33cf990f6dd94259fea01105b81d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Analgesics, Non-Narcotic - pharmacology</topic><topic>Animals</topic><topic>Cytochrome P-450 Enzyme System - pharmacology</topic><topic>Cytochrome P-450 Enzyme System - physiology</topic><topic>Eicosanoids - pharmacology</topic><topic>Fever - chemically induced</topic><topic>Fever - physiopathology</topic><topic>Injections, Intraventricular</topic><topic>Lipopolysaccharides</topic><topic>Male</topic><topic>Protein Isoforms - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kozak, Wieslaw</creatorcontrib><creatorcontrib>Kluger, Matthew J</creatorcontrib><creatorcontrib>Kozak, Anna</creatorcontrib><creatorcontrib>Wachulec, Maciej</creatorcontrib><creatorcontrib>Dokladny, Karol</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kozak, Wieslaw</au><au>Kluger, Matthew J</au><au>Kozak, Anna</au><au>Wachulec, Maciej</au><au>Dokladny, Karol</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of cytochrome P-450 in endogenous antipyresis</atitle><jtitle>American journal of physiology. Regulatory, integrative and comparative physiology</jtitle><addtitle>Am J Physiol Regul Integr Comp Physiol</addtitle><date>2000-08-01</date><risdate>2000</risdate><volume>279</volume><issue>2</issue><spage>455</spage><epage>R460</epage><pages>455-R460</pages><issn>0363-6119</issn><eissn>1522-1490</eissn><abstract>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</abstract><cop>United States</cop><pmid>10938232</pmid><doi>10.1152/ajpregu.2000.279.2.R455</doi></addata></record> |
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source | MEDLINE; American Physiological Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals |
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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