Yao Xiao-Min, Wang Bao-Lian, Gu Yu, Li Yan
Department of New Drug Development, Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.
Yao Xue Xue Bao. 2011 Jun;46(6):656-63.
The present study was performed to investigate the effect of bicyclol on hepatic microsomal cytochrome P450 (CYP) activity, as well as gene and protein expressions in rats after partial hepatectomy (PH). Bicyclol (300 mg x kg(-1)) was given to rats subjected to 70% hepatectomy three times before operation. At 6 and 48 h after PH, blood and liver tissue samples were collected for the measurement of serum alanine aminotransferase (ALT), hepatic microsomal malondialdehyde (MDA) and total hepatic CYP content. The activities of four CYP isozymes were detected with liquid chromatography-mass spectrometry (LC-MS) and the gene and protein expressions were determined by RT-PCR and Western blotting assay. As a result, bicyclol pretreatment markedly inhibited the elevation of serum ALT and hepatic microsomal MDA, and prevented the decrease of total hepatic CYP content in PH rats. In addition, bicyclol significantly attenuated the reduction of CYP2C6 activity and mRNA expression, as well as the reduction of CYP2C11 activity in PH rats. Bicyclol can inhibit the decrease of CYP3A1/2 activity, and up-regulate the mRNA and protein expressions of CYP3A1 and CYP2E1. These results showed that bicyclol pretreatment might ameliorate abnormality in CYP450 isoforms during liver regeneration after PH, and this protective effect was likely due to its anti-oxidative property and enzyme induction.
本研究旨在探讨双环醇对大鼠部分肝切除(PH)后肝微粒体细胞色素P450(CYP)活性以及基因和蛋白表达的影响。在手术前,对接受70%肝切除的大鼠给予双环醇(300 mg·kg⁻¹),共三次。在PH术后6小时和48小时,采集血液和肝组织样本,用于检测血清丙氨酸氨基转移酶(ALT)、肝微粒体丙二醛(MDA)和肝脏总CYP含量。采用液相色谱-质谱联用(LC-MS)检测四种CYP同工酶的活性,通过逆转录-聚合酶链反应(RT-PCR)和蛋白质免疫印迹法检测基因和蛋白表达。结果显示,双环醇预处理显著抑制了PH大鼠血清ALT和肝微粒体MDA的升高,并防止了肝脏总CYP含量的降低。此外,双环醇显著减轻了PH大鼠中CYP2C6活性和mRNA表达的降低以及CYP2C11活性的降低。双环醇可抑制CYP3A1/2活性的降低,并上调CYP3A1和CYP2E1的mRNA和蛋白表达。这些结果表明,双环醇预处理可能改善PH后肝再生过程中CYP450同工酶的异常,这种保护作用可能归因于其抗氧化特性和酶诱导作用。