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作 者:董海燕[1] 邵敬伟[1] 陈剑峰[1] 王涛[1] 林凤屏[1] 郭养浩[1]
机构地区:[1]福州大学药物生物技术与工程研究所,福建福州350002
出 处:《中国中药杂志》2008年第9期1014-1017,1089,共5页China Journal of Chinese Materia Medica
基 金:福建省科技项目(2007F3047);福州大学校人才基金(HX2005-3)
摘 要:目的:从中药中筛选通过激活人孕烷X受体(PXR)诱导细胞色素P450 3A4(CYP3A4)转录表达的中药;研究其诱导能力与药物浓度和作用时间之间的关系。方法:在HepG2细胞中,采用瞬时共转染报告基因试验筛选对CYP3A4转录表达有诱导作用的中药,研究其在不同浓度和不同作用时间下对PXR介导的CYP3A4的转录调节作用。结果:中药莪术、苍术、白术和茯苓均能通过激活PXR诱导CYP3A4的转录表达,且具有浓度-效应关系和时间-效应关系。在浓度-效应关系中,500 mg.L-1的莪术、苍术、白术和茯苓,在作用时间24 h时,其诱导倍数分别为0.1%DMSO处理细胞的(6.82±0.09),(6.76±0.20),(5.49±0.13),(4.97±0.07)倍。在时间-效应关系研究中,500 mg.L-1的莪术、苍术、白术和茯苓,在作用时间为48 h时,其诱导倍数分别为0.1%DMSO作用细胞的(7.74±0.54),(7.34±0.10),(5.54±0.11),(5.32±0.18)倍。结论:中药莪术、苍术、白术和茯苓均能够通过激活PXR诱导CYP3A4的转录表达。Objective: To screen a group of traditional Chinese medicines with effect on pregnane X receptor (PXR) -mediated transcription regulation of P450 3A4 (CYP3A4) ; and to study whether they can induce the expression of CYP3A4 with a dose, timedependent manner. Method: Transient cotransfection reporter gene assays were performed with pCI-hPXR-neo, pGL3-CYP3A4-Luc and β-galactosidase expression plasmid in HepG2 cells. Result: Rhizoma Curcumae, Atractylodes lancea, A. macrocaphala and Poria cocos could induce transcriptional expression of CYP3A4. In the dose-effect study, 24 h after induction, 500 mg · L^-1 Rhizoma Curcumae, A. lancea, A. macrocaphala and Poria cocos, respectively, could induce the CYP3A4 gene expression with (6. 82 ±0. 09), (6. 76 ±0. 20), (5.49 ±0. 13) and (4. 97 ±0. 07) folds, as compared with 0. 1% DMSO treatedcells. In the time-effect study, 500 mg · L^-1 Rhizoma curcumae, A. lancea, A. macrocaphala and Poria cocos for 48 h could induce the CYP3A4 gene expression with (7.74 ±0. 54), (7.34 ±0. 10), (5.54±0. 11 ) and (5.32±0. 18) folds, compared with 0. 1% DMSO treated cells. Conclusion: Rhizoma Curcumae, A. lancea, A. macrocaphala and Poria cocos could induce the expression of CYP3A4 gene transcription through activating PXR.
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