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Inhibitors of alternative pathways of arachidonate metabolism differentially affect fever in mice
W Kozak1, I Archuleta, K P Mayfield
1Lovelace Respiratory Research Institute, Inhalation Toxicology Laboratory, Albuquerque, New Mexico 87185, USA.
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.
Insights
Selective inhibitors of lipoxygenase and epoxygenase pathways were tested for their effect on fever in mice. The cytochrome P-450/epoxygenase pathway appears to be involved in antipyresis and fever regulation.
Area of Science:
- Biochemistry
- Pharmacology
- Physiology
Background:
- Cyclooxygenase (COX) inhibitors are known fever reducers.
- The roles of other arachidonic acid oxygenation pathways, specifically lipoxygenase (LOX) and epoxygenase, in fever regulation remain less understood.
Purpose of the Study:
- To investigate the effects of selective and dual inhibitors of LOX and epoxygenase pathways on fever development in mice.
- To test the hypothesis that these pathways influence fever's magnitude and duration.
Main Methods:
- Swiss Webster mice were used, with body temperature monitored via biotelemeters.
- Fever was induced using lipopolysaccharide (LPS) injections.
- Various inhibitors, including phenidone, esculetin, nordihydroguaiaretic acid (NDGA), SKF-525A, clotrimazole, and indomethacin, were administered.
Main Results:
- Phenidone, a dual LOX/COX inhibitor, prevented fever.
- Esculetin, a selective LOX inhibitor, did not affect fever.
- NDGA (dual LOX/epoxygenase), SKF-525A, and clotrimazole (cytochrome P-450/epoxygenase inhibitors) augmented fever.
- Indomethacin (COX inhibitor) reduced clotrimazole-induced fever potentiation, indicating a prostaglandin-mediated effect.
Conclusions:
- The cytochrome P-450/epoxygenase pathway plays a role in antipyresis and in limiting fever's upper range.
- Fever potentiation by epoxygenase inhibitors is likely mediated by prostaglandins.