Herb-Drug Interactions: In Vivo and In Vitro Effect of Shenmai Injection, a Herbal Preparation, on the Metabolic Activities of Hepatic Cytochrome P450 3A1/2, 2C6, 1A2, and 2E1 in Rats

被引:76
作者
Xia, Chun-hua [1 ,2 ]
Sun, Jian-guo [1 ]
Wang, Guang-ji [1 ]
Shang, Li-li [1 ]
Zhang, Xiao-xuan [1 ]
Zhang, Rong [1 ]
Peng, Ying [1 ]
Wang, Xiao-jin [1 ]
Hao, Hai-ping [1 ]
Xie, Lin [1 ]
Roberts, Michael S. [3 ]
机构
[1] China Pharmaceut Univ, Key Lab Drug Metab & Pharmacokinet, Nanjing 210009, Peoples R China
[2] Nanchang Univ, Coll Med, Clin Pharmacol Inst, Nanchang, Peoples R China
[3] Univ Queensland, Princess Alexandra Hosp, So Clin Div, Therapeut Res Unit, Brisbane, Qld, Australia
基金
英国医学研究理事会;
关键词
Shenmai injection; Radix Ginseng (Panax ginseng CA Mey; Araliaceae); Radix Ophiopogonis (Ophiopogon japonicus Ker-Gawl; Liliaceae); metabolism-based interactions; CYP450; pharmacokinetics; GARLIC SUPPLEMENTS; PANAX-GINSENG; PHARMACOKINETICS; WARFARIN; COCKTAIL; PHARMACODYNAMICS; CHLORZOXAZONE; THEOPHYLLINE; MIDAZOLAM; ISOFORMS;
D O I
10.1055/s-0029-1186082
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Shenmai injection (SMI), a mixture of Radix Ginseng and Radix Ophiopogonis, is one of the most popular herbal medicinal products and is widely used for the treatment of coronary atherosclerotic cardiopathy and viral myocarditis. The purpose of this study was to investigate the effect of SMI, in vivo and in vitro, on the metabolic activities of hepatic cytochrome CYP450 3A1/2, 2C6, 2E1, and 1A2 in rats. After a single or multiple pretreatment with SMI, the rats were administrated intravenously a cocktail containing midazolam (1 mg/kg), diclofenac (0.5 mg/kg), theophylline (1 mg/kg), and chlorzoxazone (0.5 mg/kg) as probe substrates of rat CYP450 3A1/2, 2C6, 1A2, and 2E1, respectively. Single and multiple SMI pretreatment to rats resulted in a rise of 33.8% (p < 0.01) and 25.6% (p < 0.01) in AUC for midazolam, and an increase in AUC for diclofenac by 14.7% (p < 0.05) and 31.2% (p < 0.01), respectively. However, the pharmacokinetics of chlorzoxazone and theophylline in rats was not altered markedly. In rat liver microsomes, linear mixed-type inhibition of SMI against the enzyme activities of CYP3A1/2, CYP2C6, and CYP1A2 was shown with IC50 values of 3.3%, 2.0%, and 3.1% and K-i values of 3.8%, 1.5%. and 1.9%, respectively. These in vivo and in vitro results demonstrated that SMI had the potential to inhibit the activities of hepatic CYP3A1/2 and CYP2C6, but might not significantly affect CYP1A2 and CYP2E1-mediated metabolism in rats.
引用
收藏
页码:245 / 250
页数:6
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