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马钱子碱联合甘草次酸或甘草苷对大鼠体内肝细胞色素P450活性的影响。

Effects of brucine combined with glycyrrhetinic acid or liquiritin on rat hepatic cytochrome P450 activities in vivo.

作者信息

Xing Pan-pan, Wu Wen-hua, Du Peng, Han Feng-mei, Chen Yong

机构信息

Hubei Province Key Laboratory of Biotechnology of Chinese Traditional Medicine, Hubei University, Wuhan 430062, China.

出版信息

Yao Xue Xue Bao. 2011 May;46(5):573-80.

Abstract

Abstract: The activities of four CYP450 enzymes (CYP3A, 1A2, 2El and 2C) and the mRNA expression levels of CYP1A2, 2El, 2Cll and 3A1 in rat liver were determined after Wistar rats were orally administered with brucine (BR) at three dosage levels (3, 15 and 60 mg.kg-1 per day) and the high dose of BR combined with glycyrrhetinic acid (GA, 25 mg.kg-1 per day) or liquiritin (LQ, 20 mg.kg-1 per day) for 7 consecutive days. Compared with the control, brucine caused 24.5% and 34.6% decrease of CYP3A-associated testosterone 6beta-hydroxylation (6betaTesto-OH) and CYP2C-associated tolbutamide hydroxylation (Tol-OH), respectively, and 146.1% increase of CYP2El-associated para-nitrophenol hydroxylation (PNP-OH) at the high dose level. On the other hand, (BR+GA) caused 51.4% and 33.5% decrease, respectively, of CYP2El-associated PNP-OH and CYP1A2-associated ethoxyresorufin-O-de-ethylation (EROD) as compared with the high dose of BR group. Meanwhile, (BR+LQ) caused 41.1% decrease of CYP2El-associated PNP-OH and 37.7% increase of CYP2C-associated Tol-OH. The results indicated that the co-administration of BR with GA or LQ had effect on mRNA expression and activities of the CYP450 enzymes mentioned above to some extent, and the in vivo antagonism of LQ on BR-induced CYPs adverse effects and the in vivo inhibitory action of GA on CYP2E1 and 1A2 might play an important role in the detoxification of Radix Glycyrrhizae against Strychnos nux-vomica L.

摘要

摘要

将Wistar大鼠按三个剂量水平(每天3、15和60mg·kg-1)口服马钱子碱(BR),并将高剂量的BR与甘草次酸(GA,每天25mg·kg-1)或甘草苷(LQ,每天20mg·kg-1)连续联合给药7天,之后测定大鼠肝脏中四种细胞色素P450酶(CYP3A、1A2、2E1和2C)的活性以及CYP1A2、2E1、2C11和3A1的mRNA表达水平。与对照组相比,高剂量水平的马钱子碱使CYP3A相关的睾酮6β-羟基化(6βTesto-OH)和CYP2C相关的甲苯磺丁脲羟基化(Tol-OH)分别降低了24.5%和34.6%,使CYP2E1相关的对硝基苯酚羟基化(PNP-OH)增加了146.1%。另一方面,与高剂量的马钱子碱组相比,(BR+GA)使CYP2E1相关的PNP-OH和CYP1A2相关的乙氧异羟肟酸-O-脱乙基酶(EROD)分别降低了51.4%和33.5%。同时,(BR+LQ)使CYP2E1相关的PNP-OH降低了41.1%,使CYP2C相关的Tol-OH增加了37.7%。结果表明,BR与GA或LQ联合给药在一定程度上对上述CYP450酶的mRNA表达和活性有影响,LQ对BR诱导的CYPs不良反应的体内拮抗作用以及GA对CYP2E1和1A2的体内抑制作用可能在甘草解毒马钱子中发挥重要作用。

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