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β-肾上腺素受体阻断药与细胞色素P-450:普萘洛尔治疗对肝病患者咖啡因、安替比林、D-葡萄糖醛酸和吲哚菁绿消除的影响

Beta-adrenoceptor blocking drugs and cytochrome P-450: the influence of propranolol treatment on caffeine, antipyrine, D-glucaric acid and indocyanine green elimination in patients with hepatic disorders.

作者信息

Traeger A, Horváth T, Rechenbach C, Jávor T

出版信息

Int J Clin Pharmacol Res. 1986;6(3):235-9.

PMID:3744626
Abstract

The effect of the beta-adrenoceptor blocking drug propranolol was investigated in patients with alcoholic liver disease and in those without liver disease before and after ten days treatment with 80 mg daily. Caffeine as a marker drug for the 3-methylcholanthrene-inducible subtype had a significantly enhanced clearance after propranolol in liver-diseased patients, while the clearance of antipyrine which represents the phenobarbital-inducible subtype was unchanged. D-glucaric acid excretion as an endogenous compound which serves as an indicator of induced state of drug-metabolizing capacity of the liver was slightly enhanced in liver patients, but significantly decreased in patients without liver disorders. Indocyanine green elimination as a test material for substances limiting liver blood flow was not significantly reduced by this propranolol dosage.

摘要

研究了β-肾上腺素能受体阻滞剂普萘洛尔对酒精性肝病患者及无肝病患者的影响,这些患者每日服用80mg普萘洛尔,治疗十天前后进行观察。咖啡因作为3-甲基胆蒽诱导亚型的标记药物,在肝病患者中服用普萘洛尔后清除率显著提高,而代表苯巴比妥诱导亚型的安替比林清除率未变。D-葡糖醛酸排泄作为一种内源性化合物,可作为肝脏药物代谢能力诱导状态的指标,在肝病患者中略有升高,但在无肝病患者中显著降低。作为限制肝血流物质测试材料的吲哚菁绿清除率,未因该剂量的普萘洛尔而显著降低。

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