Abstract |
KME-4,alpha-(3,5-di-t-butyl-4-hydroxybenzylidene)-gamma-buty rolactone was found to reduce the accumulation of leucocytes and exudate volume in the rat carrageenan pleurisy model. When administered orally 1 h before carrageenan, KME-4 (3-10 mg kg-1) induced a degree of inhibition of leucocyte migration almost equal to that of indomethacin (3-10 mg kg-1) in both 5 h and 24 h pleurisies. Furthermore, KME-4, when administered orally 5 h after the carrageenan, inhibited both monocyte numbers and exudate volume in a 24 h pleurisy and was more effective than indomethacin and BW755c which inhibited only monocyte migration. These results suggest that KME-4 has a differential anti-inflammatory activity. Dexamethasone (0.25 mg kg-1) showed strong inhibition of total cell numbers and exudate volume.
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Authors | T Hidaka, K Hosoe, I Katsumi, T Yamashita, K Watanabe |
Journal | The Journal of pharmacy and pharmacology
(J Pharm Pharmacol)
Vol. 38
Issue 3
Pg. 244-7
(Mar 1986)
ISSN: 0022-3573 [Print] England |
PMID | 2871169
(Publication Type: Journal Article)
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Chemical References |
- Anti-Inflammatory Agents
- Furans
- KME 4
- Carrageenan
- 4-Butyrolactone
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Topics |
- 4-Butyrolactone
(analogs & derivatives, pharmacology)
- Animals
- Anti-Inflammatory Agents
(pharmacology)
- Carrageenan
- Cell Migration Inhibition
- Furans
(pharmacology)
- Leukocytes
(immunology)
- Male
- Pleurisy
(etiology, immunology)
- Rats
- Rats, Inbred Strains
- Time Factors
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