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中药小柴胡汤对人体两种细胞色素P450酶(1A2和3A)及黄嘌呤氧化酶的体内作用。

The in-vivo effects of sho-saiko-to, a traditional Chinese herbal medicine, on two cytochrome P450 enzymes (1A2 and 3A) and xanthine oxidase in man.

作者信息

Saruwatari Junji, Nakagawa Kazuko, Shindo Junichi, Nachi Shinobu, Echizen Hirotoshi, Ishizaki Takashi

机构信息

Division of Clinical Pharmacology, Graduate School of Pharmaceutical Sciences, Faculty of Medical and Pharmaceutical Sciences, Kumamoto University, Oe-honmachi 5-1, Kumamoto 862-0973, Japan.

出版信息

J Pharm Pharmacol. 2003 Nov;55(11):1553-9. doi: 10.1211/0022357022061.

Abstract

The Chinese herbal medicine sho-saiko-to is a mixture of seven herbal components (Bupleurum root, Pinellia tuber, Scutellaria root, Jujube fruit, Ginseng root, Glycyrrhiza root and Ginger rhizome) that is widely administered to patients with chronic hepatitis in Japan. We assessed the effects of sho-saiko-to on the activity of cytochrome P450 (CYP) 1A2, CYP3A and xanthine oxidase (XO) in man. Twenty-six healthy subjects were studied to evaluate their baseline activity of CYP1A2 and XO by the respective urinary metabolic ratios of an 8-h urine sample after an oral 150-mg dose of caffeine and of CYP3A by a urinary excretion ratio of 6beta-hydroxycortisol (6beta-HC) to free cortisol (FC). Thereafter, the subjects received a twice-daily 2.5-g dose of sho-saiko-to for five days, and underwent the caffeine test on day 1 and day 5. The mean activity of CYP1A2 decreased by 16% on both day 1 and day 5 compared with the baseline (P=0.001). The mean activity of XO also significantly decreased by 25% on day 1 and 20% on day 5 (P<0.0001) compared with the baseline value. The activity of CYP3A tended to be lower on day 5 than the baseline (P=0.146). It is concluded that sho-saiko-to reduces CYP1A2 and XO activity in man.

摘要

中药小柴胡汤是由七种草药成分(柴胡、半夏、黄芩、大枣、人参、甘草和生姜)混合而成,在日本广泛用于慢性肝炎患者。我们评估了小柴胡汤对人体细胞色素P450(CYP)1A2、CYP3A和黄嘌呤氧化酶(XO)活性的影响。研究了26名健康受试者,通过口服150毫克咖啡因后8小时尿液样本的各自尿代谢率评估其CYP1A2和XO的基线活性,通过6β-羟基皮质醇(6β-HC)与游离皮质醇(FC)的尿排泄率评估CYP3A的基线活性。此后,受试者每天两次服用2.5克小柴胡汤,持续五天,并在第1天和第5天进行咖啡因测试。与基线相比,CYP1A2的平均活性在第1天和第5天均下降了16%(P=0.001)。与基线值相比,XO的平均活性在第1天也显著下降了25%,在第5天下降了20%(P<0.0

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