TY - JOUR
T1 - Herb-drug interactions
T2 - 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
AU - Xia, Chun Hua
AU - Sun, Jian Guo
AU - Wang, Guang Ji
AU - Shang, Li Li
AU - Zhang, Xiao Xuan
AU - Zhang, Rong
AU - Peng, Ying
AU - Wang, Xiao Jin
AU - Hao, Hai Ping
AU - Xie, Lin
AU - Roberts, Michael S.
PY - 2010
Y1 - 2010
N2 - 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 (1mg/kg), diclofenac (0.5mg/kg), theophylline (1mg/kg), and chlorzoxazone (0.5mg/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 ICvalues of 3.3%, 2.0%, and 3.1% and Kvalues 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.
AB - 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 (1mg/kg), diclofenac (0.5mg/kg), theophylline (1mg/kg), and chlorzoxazone (0.5mg/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 ICvalues of 3.3%, 2.0%, and 3.1% and Kvalues 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.
KW - Araliaceae)
KW - CYP450
KW - Liliaceae)
KW - Metabolismbased interactions
KW - Pharmacokinetics
KW - Radix Ginseng (Panax ginseng C.A. Mey.
KW - Radix Ophiopogonis (Ophiopogon japonicus KerGawl.
KW - Shenmai injection
UR - https://www.scopus.com/pages/publications/77049117035
U2 - 10.1055/s-0029-1186082
DO - 10.1055/s-0029-1186082
M3 - 文章
C2 - 19774504
AN - SCOPUS:77049117035
SN - 0032-0943
VL - 76
SP - 245
EP - 250
JO - Planta Medica
JF - Planta Medica
IS - 3
ER -