PXR mediated induction of CYP3A4, CYP1A2, and P-gp by Mitragyna speciosa and its alkaloids

被引:39
作者
Manda, Vamshi K. [1 ]
Avula, Bharathi [1 ]
Dale, Olivia R. [1 ]
Ali, Zulfiqar [1 ]
Khan, Ikhlas A. [1 ,2 ]
Walker, Larry A. [1 ,2 ]
Khan, Shabana I. [1 ,2 ]
机构
[1] Univ Mississippi, Natl Ctr Nat Prod Res, Sch Pharm, Oxford, MS 38677 USA
[2] Univ Mississippi, Dept Biomol Sci, Sch Pharm, Oxford, MS 38677 USA
关键词
Cytochrome P450; Drug interactions; Kratom; Mitragyna speciosa; P-gp; PXR; PREGNANE-X-RECEPTOR; ARYL-HYDROCARBON RECEPTOR; CYTOCHROME-P450; ENZYMES; OXINDOLE ALKALOIDS; DRUG-INTERACTIONS; HUMAN HEPATOCYTES; CELL-LINE; KRATOM; 3-METHYLCHOLANTHRENE; IDENTIFICATION;
D O I
10.1002/ptr.5942
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Kratom (Mitragyna speciosa), a native herb of Southeast Asia, is widely known for its psychoactive properties. Recent increase in the use of kratom as a recreational drug has increased the risk of its interaction with conventional drugs if taken concomitantly. A few reports are available related to the effects of kratom on the activity of cytochrome P450 enzymes (CYPs), but there are no reports of its effects on pregnane X receptor (PXR), a transcription factor that regulates the expression of CYPs and P-glycoprotein (P-gp). This study was carried out to evaluate the effects of a methanolic extract of kratom leaves, an alkaloid rich fraction and its 5 indole and 4 oxindole alkaloids on PXR activation and the resulting changes in the mRNA expression of PXR target genes (CYP3A4, CYP1A2, and P-gp). A significant activation of PXR was observed by the extract (3-fold), alkaloidal fraction (4-fold) and all 9 alkaloids (4- to 6-fold) that was associated with an increased mRNA expression which resulted into an increase in the activity of CYP3A4, CYP1A2, and P-gp. These results indicate that high consumption of Mitragyna speciosa extract along with the conventional drugs may lead to potential herb-drug interactions due to its effects on PXR.
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页码:1935 / 1945
页数:11
相关论文
共 31 条
[1]   Isolation, characterization, and NMR spectroscopic data of indole and oxindole alkaloids from Mitragyna speciosa [J].
Ali, Zulfiqar ;
Demiray, Hatice ;
Khan, Ikhlas A. .
TETRAHEDRON LETTERS, 2014, 55 (02) :369-372
[2]  
Anwar M, 2016, MMWR-MORBID MORTAL W, V65, P748, DOI 10.15585/mmwr.mm6529a4
[3]   Identification and Characterization of Indole and Oxindole Alkaloids from Leaves of Mitragyna speciosa Korth Using Liquid Chromatography-Accurate QToF Mass Spectrometry [J].
Avula, Bharathi ;
Sagi, Satyanarayanaraju ;
Wang, Yan-Hong ;
Wang, Mei ;
Ali, Zulfiqar ;
Smillie, Troy J. ;
Zweigenbaum, Jerry ;
Khan, Ikhlas A. .
JOURNAL OF AOAC INTERNATIONAL, 2015, 98 (01) :13-21
[4]  
Bishop-Freeman S. C., 2016, J ANAL TOXICOLOGY
[5]   Clinical Herbal Interactions with Conventional Drugs: From Molecules to Maladies [J].
Chen, X-W ;
Serag, E. S. ;
Sneed, K. B. ;
Liang, J. ;
Chew, H. ;
Pan, S-Y ;
Zhou, S-F .
CURRENT MEDICINAL CHEMISTRY, 2011, 18 (31) :4836-4850
[6]   Nuclear receptors in the multidrug resistance through the regulation of drug-metabolizing enzymes and drug transporters [J].
Chen, Yakun ;
Tang, Yong ;
Guo, Changxiong ;
Wang, Jiuhui ;
Boral, Debasish ;
Nie, Daotai .
BIOCHEMICAL PHARMACOLOGY, 2012, 83 (08) :1112-1126
[7]  
Darwich AS, 2010, CURR DRUG METAB, V11, P716
[8]  
Galbis-Reig David, 2016, WMJ, V115, P49
[9]   The orphan human pregnane X receptor mediates the transcriptional activation of CYP3A4 by rifampicin through a distal enhancer module [J].
Goodwin, B ;
Hodgson, E ;
Liddle, C .
MOLECULAR PHARMACOLOGY, 1999, 56 (06) :1329-1339
[10]   Recent Structural Insights into Cytochrome P450 Function [J].
Guengerich, F. Peter ;
Waterman, Michael R. ;
Egli, Martin .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2016, 37 (08) :625-640