尿酸
丙磺舒
代谢物
化学
药理学
多尿
内分泌学
内科学
尿酸
生物
生物化学
医学
高尿酸血症
糖尿病
作者
George M. Fanelli,D L Bohn,Sheila S. Reilly
标识
DOI:10.1016/s0022-3565(25)28691-8
摘要
The effects of known uricosuric agents have been examined by standard clearance techniques in male Cebus monkeys. Probenecid was effective in promoting uricosuria at p.o. doses greater than 10 mg/kg. Sulfinpyrasone was only mildly active in this species. Zoxazolamine, at p.o. doses sufficient to produce marked uricosuria in man, was inactive. Phenylbutasone was weakly active; carinamide did not elicit a uricosuric response under our experimental conditions. Iodopyracet at high loads was markedly uricosuric. Chlorothiaside at i.v. doses of 25 mg/kg elicited a biphasic response of uricosuria followed by urate retention. The relative inactivity of certain uricosuric agents in the Cebus monkey is thought to be due to either a basic difference from man in the urate transport system or the result of rapid biotransformation to an inactive metabolite(s), poor oral adsorption or a combination of these.
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