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硫喷妥治疗期间的血液戊巴比妥浓度。

Blood pentobarbital concentrations during thiopental therapy.

作者信息

Watson W A, Godley P J, Garriott J C, Bradberry J C, Puckett J D

出版信息

Drug Intell Clin Pharm. 1986 Apr;20(4):283-7. doi: 10.1177/106002808602000414.

Abstract

The desulfuration of thiopental to pentobarbital has previously been shown to be a relatively minor pathway of thiopental metabolism. In two cases, we observed significant conversion, resulting in blood pentobarbital concentrations up to 50 percent of total blood barbiturate (thiopental and pentobarbital) concentrations. Both patients received continuous infusions of thiopental and had present a condition (hypothermia) or drug (cimetidine) known to inhibit hepatic microsomal enzyme activity. It is suggested that inhibition of hepatic microsomal enzyme activity may prevent thiopental's metabolism to its major metabolite, a carboxylic acid analogue, and increase the amount of thiopental desulfurated to pentobarbital. Inhibition of hepatic microsomal metabolism also decreases the metabolism of pentobarbital. Until further elucidation of the causes of altered thiopental metabolism is available to identify patients more likely to have elevated concentrations of pentobarbital, monitoring of blood drug concentrations in patients receiving thiopental should include determination of both thiopental and pentobarbital concentrations.

摘要

硫喷妥转化为戊巴比妥的脱硫作用此前已被证明是硫喷妥代谢的一条相对次要的途径。在两例病例中,我们观察到了显著的转化,导致血液中戊巴比妥浓度高达总血液巴比妥酸盐(硫喷妥和戊巴比妥)浓度的50%。两名患者均接受了硫喷妥的持续输注,且都存在已知会抑制肝微粒体酶活性的情况(低温)或药物(西咪替丁)。提示肝微粒体酶活性的抑制可能会阻止硫喷妥代谢为其主要代谢产物——一种羧酸类似物,并增加硫喷妥脱硫转化为戊巴比妥的量。肝微粒体代谢的抑制也会降低戊巴比妥的代谢。在能够进一步阐明硫喷妥代谢改变的原因以识别更可能有升高的戊巴比妥浓度的患者之前,对接受硫喷妥治疗的患者进行血药浓度监测应包括硫喷妥和戊巴比妥浓度的测定。

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