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表雄酮诱导的发热对血浆安替比林半衰期及代谢清除率的影响。

Effects of etiocholanolone-induced fever on plasma antipyrine half-lives and metabolic clearance.

作者信息

Elin R J, Vesell E S, Wolff S M

出版信息

Clin Pharmacol Ther. 1975 Apr;17(4):447-57. doi: 10.1002/cpt1975174447.

Abstract

The plasma half-life and metabolic clearance rate of antipyrine, a drug metabolized by hepatic microsomal enzymes, were determined in 33 normal volunteers during a basal state and during fever induced with a single intramuscular injection of etiocholanolone. Of the 14 normal volunteers who achieved significant fever (fever index greater than 50), in 11 plasma antipyrine half-life was prolonged after a single oral dose of 10 mg/kg and antipyrine metabolic clearance rate was decreased. There was no significant change of these mean values in 19 normal volunteers who failed to develop significant fever (fever index smaller than 50). Therefore, under the conditions of this study plasma antipyrine half-life was prolonged, probably due to impaired hepatic metabolism, during etiocholanolone-induced fever, although no correlation was observed between the magnitude of fever and the extent to which plasma antipyrine half-life was prolonged. Failure to obtain such a correlation may be attributable to the very small range of temperature elevation, extending from 37.9 degrees C to 39.2 degrees C, in the group of 14 subjects achieving significant etiocholanolone-induced fever (fever index greater than 50). A higher dose of antipyrine (18 mg/kg) suppressed induction of fever by etiocholanolone; antipyrine is the only orally administered drug thus far shown to be effective in repressing etiocholanolone-induced fever.

摘要

安替比林是一种经肝微粒体酶代谢的药物,在33名正常志愿者处于基础状态以及单次肌内注射本胆烷醇酮诱导发热期间,测定了其血浆半衰期和代谢清除率。在14名出现显著发热(发热指数大于50)的正常志愿者中,11名在单次口服10mg/kg安替比林后血浆半衰期延长,安替比林代谢清除率降低。在19名未出现显著发热(发热指数小于50)的正常志愿者中,这些平均值无显著变化。因此,在本研究条件下,在本胆烷醇酮诱导发热期间,血浆安替比林半衰期延长,可能是由于肝脏代谢受损,尽管未观察到发热程度与血浆安替比林半衰期延长程度之间的相关性。未能获得这种相关性可能归因于在14名出现显著本胆烷醇酮诱导发热(发热指数大于50)的受试者组中,体温升高范围非常小,从37.9℃到39.2℃。较高剂量的安替比林(18mg/kg)可抑制本胆烷醇酮诱导的发热;安替比林是迄今为止唯一显示对抑制本胆烷醇酮诱导的发热有效的口服药物。

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