Dual effects of extract of Schisandra chinensis Baill on rat hepatic CYP3A.
- Author:
Qian CHEN
1
;
Yu-jing WU
;
Neng-neng CHENG
;
Ya-lin LI
;
Yong-ming WANG
Author Information
1. Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai 201203, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Cyclooctanes;
administration & dosage;
isolation & purification;
pharmacology;
Cytochrome P-450 CYP3A;
genetics;
metabolism;
Dioxoles;
administration & dosage;
isolation & purification;
pharmacology;
Dose-Response Relationship, Drug;
Drugs, Chinese Herbal;
administration & dosage;
isolation & purification;
pharmacology;
Hepatocytes;
drug effects;
enzymology;
Inhibitory Concentration 50;
Lignans;
administration & dosage;
isolation & purification;
pharmacology;
Male;
Microsomes, Liver;
enzymology;
Plants, Medicinal;
chemistry;
Polycyclic Compounds;
administration & dosage;
isolation & purification;
pharmacology;
RNA, Messenger;
metabolism;
Rats;
Rats, Sprague-Dawley;
Schisandra;
chemistry
- From:
Acta Pharmaceutica Sinica
2010;45(9):1194-1198
- CountryChina
- Language:Chinese
-
Abstract:
This study is to investigate the effects of aqueous extract of Schisandra chinensis Baill (WWZ), kadsurin, schisandrin A, schisandrin B and schisandrol B on rat hepatic CYP3A. Rats received a daily gavage of aqueous extract of WWZ for different times. The livers were harvested after gavage and subjected to microsome preparation. Microsomal CYP3A activity was determined by measuring the amount of the metabolite of testosterone (6 beta-hydroxytestosterone) with HPLC. Aqueous extract of WWZ, kadsurin and schisandrin A were incubated with microsomes obtained from rat. Microsomal CYP3A activity was determined by HPLC. Primary hepatocytes were separated and extracted from rat, then were treated with aqueous extract of WWZ, schisandrin A, schisandrin B and schisandrol B. Then, the expression of CYP3A1 mRNA was analyzed by RT-PCR. As for the in vivo assay, aqueous extract of WWZ significantly inhibited the enzyme activity of CYP3A after 12 h gavage. The inhibitory effect was converted to inductive effect after 3-day gavage. Aqueous extract of WWZ could induce the enzyme activity of CYP3A after 6-day gavage. Aqueous extract of WWZ and kadsurin showed a dose-dependent inhibition of CYP3A (IC50 of 487.8 microg mL(-1) and 6.2 micromol L(-1), separately). In rat primary hepatocytes, aqueous extract of WWZ (2.5 mg mL(-1)), schisandrin A (0.1 micromol L(-1)), schisandrin B (0.1 micromol L(-1)) and schisandrol B (10 micromol L(-1)) increased significantly the expression of CYP3A1 mRNA by 23%, 55%, 42% and 27%, respectively. Aqueous extract of WWZ could show dual effect on the enzyme activity of CYP3A in rat in vivo. Meanwhile, kadsurin showed a dose-dependent inhibition of the enzyme activity of hepatic CYP3A in vitro. And schisandrin A, schisandrin B and schisandrol B showed significant inductive effect on the expression of rat CYP3A1 mRNA.
