Mechanism of action of colchicine
β Scribed by Yi-Han Chang
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 291 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0004-3591
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β¦ Synopsis
Abstract
Colchicine suppresses the development of carrageenanβinduced edema in the rat with a minimum effective oral dose of 6.0 mg/kg. The slope of the doseβresponse regression line for colchicine differs significantly from that of indomethacin and phenylbutazone. Based on the dosages required to achieve a 50% suppression of this inflammation, colchicine is 0.6 and 1.5 times as potent as indomethacin and phenylbutazone, respectively. In the reversed passive Arthus reaction in the rat, the suppressive activity of colchicine is at least 50 times that of indomethacin and 100 times that of phenylbutazone. The possible significance of these results with regard to the unique effectiveness of colchicine in the treatment of gout is discussed.
π SIMILAR VOLUMES
Daphnane-type diterpene gnidimacrin isolated from the Chinese plant Stellera chamaejasme L. is an antitumor agent that activates protein kinase C (PKC). The mechanism of antitumor action of gnidimacrin and the possible involvement of PKC were examined using sensitive K562 and refractory HLE cells. G