Gancao (Glycyrrhizae Radix) provides the main contribution to Shaoyao-Gancao decoction on enhancements of CYP3A4 and MDR1 expression via pregnane X receptor pathway in vitro

被引:20
作者
Feng, Dandan [1 ]
Tang, Tao [1 ]
Fan, Rong [1 ]
Luo, Jiekun [1 ]
Cui, Hanjin [1 ]
Wang, Yang [1 ]
Gan, Pingping [2 ]
机构
[1] Cent S Univ, Xiangya Hosp, Inst Integrat Med, Changsha 410008, Hunan, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Oncol, Changsha 410008, Hunan, Peoples R China
来源
BMC COMPLEMENTARY AND ALTERNATIVE MEDICINE | 2018年 / 18卷
基金
中国博士后科学基金;
关键词
Shaoyao Gancao decoction; Pregnane X receptor; Cytochrome P450 3A4; Multidrug resistance protein 1; Traditional Chinese medicine; SHAKUYAKU-KANZO-TO; CHINESE HERBAL MEDICINE; GENE-EXPRESSION; PHARMACOKINETIC COMPARISONS; COMBINATION CHEMOTHERAPY; CYTOCHROME-P450; 3A4; NUCLEAR RECEPTORS; TANG; CONSTITUENTS; ACTIVATION;
D O I
10.1186/s12906-018-2402-7
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
BackgroundChinese herbal formula Shaoyao Gancao decoction (SGD) is often used as an adjuvant with chemotherapeutic agents to treat cancer. Due to the herb-drug interactions, the alternations of drug metabolic enzyme and drug transporters induced by SGD deserve to be explored. We aimed to investigate the effect of SGD on the pregnane X receptor (PXR)-mediated transcriptional regulation of cytochrome P450 3A4 (CYP3A4) and drug transporter multidrug resistance protein 1 (MDR1) in vitro. Besides, we assessed the contribution of constituent herbs to SGD on the regulation of CYP3A4 and MDR1.MethodsThe dual luciferase reporter gene system containing the hPXR expression plasmid and the reporter gene plasmid of CYP3A4 or MDR1 was co-transfected to HepG2 and Caco2 cells. Luciferase activities were determined using a Dual-luciferase reporter assay kit. The gene expression of CYP3A4 and MDR1 in the hPXR-transfected LS174T cells were assessed by real-time qPCR. Finally, the contribution of constituent herbs from SGD was evaluated.ResultsSGD, Shaoyao and Gancao concentration-dependently increased promoter activities of CYP3A4 and MDR1 in vitro. Moreover, SGD, Shaoyao and Gancao up-regulated CYP3A4 and MDR1 mRNA in hPXR-transfected LS174T cells. As the herbal constituent of SGD, Gancao possesses significantly higher levels of metabolic enzyme and drug transporters compared with Shaoyao.ConclusionSGD tends to enhance CYP3A4 and MDR1 expression via PXR pathway, especially Gancao provides the main contribution. This study highlights a potential in vitro mechanism for SGD on the regulation of drug metabolic enzymes and drug transporters.
引用
收藏
页数:12
相关论文
共 47 条
  • [1] Safety of herbal medicine use during chemotherapy in patients with ovarian cancer: a ''bedside-to-bench'' approach
    Ben-Arye, Eran
    Lavie, Ofer
    Samuels, Noah
    Khamaisie, Hazem
    Schiff, Elad
    Raz, Orit Gressel
    Mahajna, Jamal
    [J]. MEDICAL ONCOLOGY, 2017, 34 (04)
  • [2] Antimalarial artemisinin drugs induce cytochrome p450 and MDR1 expression by activation of xenosensors pregnane X receptor and constitutive androstane receptor
    Burk, O
    Arnold, KA
    Nussler, AK
    Schaeffeler, E
    Efimova, E
    Avery, BA
    Avery, MA
    Fromm, MF
    Eichelbaum, M
    [J]. MOLECULAR PHARMACOLOGY, 2005, 67 (06) : 1954 - 1965
  • [3] Valproic acid induces CYP3A4 and MDR1 gene expression by activation of constitutive androstane receptor and pregnane X receptor pathways
    Cerveny, Lukas
    Svecova, Lucie
    Anzenbacherova, Eva
    Vrzal, Radim
    Staud, Frantisek
    Dvorak, Zdenek
    Ulrichova, Jitka
    Anzenbacher, Pavel
    Pavek, Petr
    [J]. DRUG METABOLISM AND DISPOSITION, 2007, 35 (07) : 1032 - 1041
  • [4] Nuclear receptors PXR and CAR: implications for drug metabolism regulation, pharmacogenomics and beyond
    Chai, Xiaojuan
    Zeng, Su
    Xie, Wen
    [J]. EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2013, 9 (03) : 253 - 266
  • [5] Chen Q, 2015, EVID-BASED COMPL ALT, V2015
  • [6] Absorption and Interaction of the Main Constituents from the Traditional Chinese Drug Pair Shaoyao-Gancao via a Caco-2 Cell Monolayer Model
    Chen, Yan
    Wang, Jinyan
    Wang, Lu
    Chen, Lianghui
    Wu, Qingqing
    [J]. MOLECULES, 2012, 17 (12) : 14908 - 14917
  • [7] Designing better drugs: predicting cytochrome P450 metabolism
    de Groot, Marcel J.
    [J]. DRUG DISCOVERY TODAY, 2006, 11 (13-14) : 601 - 606
  • [8] Farrell Michael P, 2003, Clin Colorectal Cancer, V2, P253, DOI 10.3816/CCC.2003.n.007
  • [9] Fujii Kazuyuki, 2004, Gan To Kagaku Ryoho, V31, P1537
  • [10] Gan PP, 2011, ASIAN J CHEM, V23, P1515