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消胆胺对胃肠道中氢化可的松摄取的相互作用。

Interaction by cholestyramine on the uptake of hydrocortisone in the gastrointestinal tract.

作者信息

Johansson C, Adamsson U, Stierner U, Lindsten T

出版信息

Acta Med Scand. 1978;204(6):509-12. doi: 10.1111/j.0954-6820.1978.tb08481.x.

Abstract

An absolute reduction of the plasma cortisol levels and a delay of the peak concentrations were recorded in 10 healthy subjects, when a bile-sequestering anionic exchange resin, cholestyramine, was given prior to a single oral hydrocortisone dose, indicating that the resin interferes with the uptake of a neutral sterol in the human gastrointestinal tract. The possibility of a direct binding of drug to resin is supported by the affinity of hydrocortisone to cholestyramine in vitro, which was uninfluenced by the presence of sodium taurocholate. Cholestyramine significantly delayed the gastric emptying of a glucose solution, indicating that the resin not only decreases but also delays hydrocortisone absorption. Careful supervision is recommended when treatment with cholestyramine is given concomitant to neutral sterol drugs.

摘要

在10名健康受试者中,当在单次口服氢化可的松剂量之前给予胆汁螯合阴离子交换树脂考来烯胺时,记录到血浆皮质醇水平绝对降低且峰值浓度延迟,这表明该树脂干扰了人体胃肠道中中性固醇的吸收。氢化可的松在体外对考来烯胺的亲和力支持了药物与树脂直接结合的可能性,这种亲和力不受牛磺胆酸钠存在的影响。考来烯胺显著延迟了葡萄糖溶液的胃排空,表明该树脂不仅降低而且延迟了氢化可的松的吸收。当考来烯胺与中性固醇类药物同时使用时,建议仔细监测。

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