1. Additional evidence for the anti-inflammatory and anti-allergic properties of the sesquiterpene polygodial.
- Author
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da Cunha FM, Fröde TS, Mendes GL, Malheiros A, Cechinel Filho V, Yunes RA, and Calixto JB
- Subjects
- Anaphylaxis etiology, Anaphylaxis prevention & control, Animals, Carrageenan adverse effects, Disease Models, Animal, Dose-Response Relationship, Drug, Edema chemically induced, Edema drug therapy, Female, Hindlimb drug effects, Hindlimb pathology, Inflammation Mediators adverse effects, Inflammation Mediators antagonists & inhibitors, Male, Mice, Ovalbumin adverse effects, Ovalbumin immunology, Pleurisy chemically induced, Pleurisy drug therapy, Rats, Rats, Wistar, Anti-Allergic Agents therapeutic use, Anti-Inflammatory Agents therapeutic use, Sesquiterpenes therapeutic use
- Abstract
This study evaluates further the anti-inflammatory and anti-allergic properties of polygodial, a sesquiterpene extracted from the barks plant Drymis winteri (Winteraceae). Polygodial (12.8-128.1 micromol/kg, i.p.) 30 min prior, inhibited significantly the mouse paw oedema induced by prostaglandin E2, bradykinin (BK) substance P (SP), dextran, platelet activating factor (PAF) or carrageenan. Polygodial also inhibited arachidonic acid-, capsaicin- and croton oil-induced ear oedema in mice. Polygodial (42.7 micromol/kg, i.p.), significantly inhibited both exudation and cell influx when assessed in the pleurisy induced by SP and histamine, and to a less extent the inflammatory response caused by carrageenan, PAF, BK and des-Arg9-BK. Finally, polygodial (4.2-42.7 micromol/kg, i.p.) produced dose-related inhibition of paw oedema induced by ovalbumin, protecting in a time-dependent manner the anaphylactic shock induced by endovenous administration of ovalbumin in animals which had been actively sensitised by this antigen. These and our previous results indicate that the major component present in the bark of the plant D. winteri, the sesquiterpene polygodial exerts an interesting anti-inflammatory and anti-allergic properties when assessed in rats and mice.
- Published
- 2001
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