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Inhibition of cytochrome P450 2B6 by Astragalus extract mixture HT042

  • Kim, Harim (Department of Biological Sciences, Konkuk University) ;
  • Lee, Yejin (Department of Biological Sciences, Konkuk University) ;
  • Kim, Vitchan (Department of Biological Sciences, Konkuk University) ;
  • Lee, Rowoon (Department of Biological Sciences, Konkuk University) ;
  • Bae, Soo Kyung (College of Pharmacy and Integrated Research Institute of Pharmaceutical Sciences, The Catholic University) ;
  • Kwak, Mi‑Kyoung (College of Pharmacy and Integrated Research Institute of Pharmaceutical Sciences, The Catholic University) ;
  • Lee, Sung Hoon (College of Pharmacy, Chung-Ang University) ;
  • Kim, Donghak (Department of Biological Sciences, Konkuk University)
  • Received : 2019.10.08
  • Accepted : 2019.10.29
  • Published : 2020.07.15

Abstract

Astragalus extract mixture (AEM) HT042 is a functional food approved by the MFDS (Korean FDA) for increasing height. It comprises a mixture of three standardized extracts from Astragalus membranaceus root, Eleutherococcus senticosus stem, and Phlomis umbrosa root. In this study, drug-functional food interaction was analyzed using six major human cytochrome P450 enzymes. The inhibitory effect of AEM HT042 on P450 activities was studied using a P450-NADPH P450 reductase reconstitution system. Among the six P450 enzymes (1A2, 2A6, 2B6, 2D6, 2C9, and 3A4), only P450 2B6 activity was markedly decreased by AEM HT042 addition. The bupropion hydroxylation activity of P450 2B6 was analyzed using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). A calculated IC50 value of 10.62 ㎍/ml was obtained. To identify the inhibitory compounds in the mixture, four active compounds in AEM HT042 were analyzed. Shanzhiside methylester exhibited inhibitory effects on P450 2B6, whereas formononetin, eleutheroside E, and sesamoside did not affect P450 2B6 activity at all. Our results suggest that shanzhiside methylester in AEM HT042 is responsible for the inhibitory effect on P450 2B6 metabolism. Characterization of the inhibitory effect on P450 can help determine the safe administration of functional foods along with many clinical drugs that are metabolized by P450.

Keywords

Acknowledgement

This research was supported by a grant from the Ministry of Food and Drug Safety in 2018 (18182MFDS384).

References

  1. Guengerich FP (2015) Human cytochrome P450 enzymes. In: Ortiz de Montellano PR (ed) Cytochrome P450: structure, mechanism, and biochemistry. Springer, London, pp 523-785
  2. Lee Y, Park HG, Kim V, Cho MA, Kim H, Ho TH, Cho KS, Lee IS, Kim D (2018) Inhibitory effect of alpha-terpinyl acetate on cytochrome P450 2B6 enzymatic activity. Chem Biol Interact 289:90-97 https://doi.org/10.1016/j.cbi.2018.04.029
  3. Ekins S, Wrighton SA (1999) The role of CYP2B6 in human xenobiotic metabolism. Drug Metab Rev 31:719-754 https://doi.org/10.1081/DMR-100101942
  4. Wang HB, Tompkins LM (2008) CYP2B6: new insights into a historically overlooked cytochrome P450 isozyme. Curr Drug Metab 9:598-610 https://doi.org/10.2174/138920008785821710
  5. Turpeinen M, Zanger UM (2012) Cytochrome P450 2B6: function, genetics, and clinical relevance. Drug Metabol Drug Interact 27:185-197
  6. Zanger UM, Schwab M (2013) Cytochrome P450 enzymes in drug metabolism: regulation of gene expression, enzyme activities, and impact of genetic variation. Pharmacol Ther 138:103-141 https://doi.org/10.1016/j.pharmthera.2012.12.007
  7. Mo SL, Liu YH, Duan W, Wei MQ, Kanwar JR, Zhou SF (2009) Substrate specificity, regulation, and polymorphism of human cytochrome P450 2B6. Curr Drug Metab 10:730-753 https://doi.org/10.2174/138920009789895534
  8. Cerny MA (2016) Prevalence of non-cytochrome P450-mediated metabolism in food and drug administration-approved oral and intravenous drugs: 2006-2015. Drug Metab Dispos 44:1246-1252 https://doi.org/10.1124/dmd.116.070763
  9. Foti RS, Dalvie DK (2016) Cytochrome P450 and non-cytochrome P450 oxidative metabolism: contributions to the pharmacokinetics, safety, and efficacy of xenobiotics. Drug Metab Dispos 44:1229-1245 https://doi.org/10.1124/dmd.116.071753
  10. Manikandan P, Nagini S (2018) Cytochrome P450 structure, function and clinical significance: a review. Curr Drug Targets 19:38-54
  11. Budzinski JW, Foster BC, Vandenhoek S, Arnason JT (2000) An in vitro evaluation of human cytochrome P450 3A4 inhibition by selected commercial herbal extracts and tinctures. Phytomedicine 7:273-282 https://doi.org/10.1016/S0944-7113(00)80044-6
  12. Foster BC, Vandenhoek S, Hana J, Krantis A, Akhtar MH, Bryan M, Budzinski JW, Ramputh A, Arnason JT (2003) In vitro inhibition of human cytochrome P450-mediated metabolism of marker substrates by natural products. Phytomedicine 10:334-342 https://doi.org/10.1078/094471103322004839
  13. Lee SY, Lee JY, Kang W, Kwon KI, Park SK, Oh SJ, Ma JY, Kim SK (2013) Cytochrome P450-mediated herb-drug interaction potential of Galgeun-tang. Food Chem Toxicol 51:343-349 https://doi.org/10.1016/j.fct.2012.10.012
  14. Song J, Lee D, Min B, Bae JS, Chang GT, Kim H (2017) Safety evaluation of Astragalus extract mixture HT042 and its constituent herbs in Sprague-Dawley rats. Phytomedicine 32:59-67 https://doi.org/10.1016/j.phymed.2017.03.005
  15. Lee D, Lee SH, Song J, Jee HJ, Cha SH, Chang GT (2018) Effects of astragalus extract mixture HT042 on height growth in children with mild short stature: a multicenter randomized controlled trial. Phytother Res 32:49-57 https://doi.org/10.1002/ptr.5886
  16. Kim MY, Park Y, Pandit NR, Kim J, Song M, Park J, Choi HY, Kim H (2010) The herbal formula HT042 induces longitudinal bone growth in adolescent female rats. J Med Food 13:1376-1384 https://doi.org/10.1089/jmf.2010.1007
  17. Kim MY, Kim JY, Lim D, Lee D, Kim Y, Chang GT, Choi HY, Kim H (2012) Skeletal growth and IGF levels in rats after HT042 treatment. Phytother Res 26:1771-1778 https://doi.org/10.1002/ptr.4642
  18. Kim JY, Song M, Lee D, Song J, Park SW, Park J, Park S, Choi HY, Kim H (2013) Effect of HT042, herbal formula, on longitudinal bone growth in spontaneous dwarf rats. Molecules 18:13271-13282 https://doi.org/10.3390/molecules181113271
  19. Lee D, Lee SH, Lee YH, Song J, Kim H (2017) Astragalus extract mixture HT042 increases longitudinal bone growth rate by upregulating circulatory IGF-1 in rats. Evid Based Complement Alternat Med 2017:6935802
  20. Park HG, Lim YR, Eun CY, Han S, Han JS, Cho KS, Chun YJ, Kim D (2010) Candida albicans NADPH-P450 reductase: expression, purification, and characterization of recombinant protein. Biochem Biophys Res Commun 396:534-538 https://doi.org/10.1016/j.bbrc.2010.04.138
  21. Park HG, Lim YR, Han S, Jeong D, Kim D (2017) Enhanced purification of recombinant rat NADPH-P450 reductase by using a hexahistidine-Tag. J Microbiol Biotechnol 27:983-989 https://doi.org/10.4014/jmb.1701.01028
  22. Shimada T, Wunsch RM, Hanna IH, Sutter TR, Guengerich FP, Gillam EM (1998) Recombinant human cytochrome P450 1B1 expression in Escherichia coli. Arch Biochem Biophys 357:111-120 https://doi.org/10.1006/abbi.1998.0808
  23. Jeong D, Park HG, Lim YR, Lee Y, Kim V, Cho MA, Kim D (2018) Terfenadine metabolism of human cytochrome P450 2J2 containing genetic variations (G312R, P351L and P115L). Drug Metab Pharmacokinet 33:61-66 https://doi.org/10.1016/j.dmpk.2017.10.004
  24. Kim D, Guengerich FP (2004) Enhancement of 7-methoxyresorufin O-demethylation activity of human cytochrome P450 1A2 by molecular breeding. Arch Biochem Biophys 432:102-108 https://doi.org/10.1016/j.abb.2004.09.001
  25. Kim D, Wu ZL, Guengerich FP (2005) Analysis of coumarin 7-hydroxylation activity of cytochrome P450 2A6 using random mutagenesis. J Biol Chem 280:40319-40327 https://doi.org/10.1074/jbc.M508171200
  26. Oh HA, Lee H, Kim D, Jung BH (2017) Development of GC-MS based cytochrome P450 assay for the investigation of multi-herb interaction. Anal Biochem 519:71-83 https://doi.org/10.1016/j.ab.2016.12.015
  27. Jiang W, Zhang S, Fu F, Zhu H, Hou J (2010) Inhibition of nuclear factor-kappaB by 6-O-acetyl shanzhiside methyl ester protects brain against injury in a rat model of ischemia and reperfusion. J. Neuroinflammation 7:55 https://doi.org/10.1186/1742-2094-7-55
  28. Fan PC, Ma HP, Hao Y, He XR, Sun AJ, Jiang W, Li MX, Jing LL, He L, Ma J, Jia ZP (2016) A new anti-fibrinolytic hemostatic compound 8-O-acetyl shanzhiside methylester extracted from Lamiophlomis rotata. J Ethnopharmacol 187:232-238 https://doi.org/10.1016/j.jep.2016.04.016
  29. Kenaan C, Zhang H, Hollenberg PF (2013) High-throughput fluorescence assay for cytochrome P450 mechanism-based inactivators. Methods Mol Biol 987:61-69 https://doi.org/10.1007/978-1-62703-321-3_5
  30. Amunugama HT, Zhang H, Hollenberg PF (2012) Mechanism-based inactivation of cytochrome P450 2B6 by methadone through destruction of prosthetic heme. Drug Metab Dispos 40:1765-1770 https://doi.org/10.1124/dmd.112.045971
  31. Zhang H, Amunugama H, Ney S, Cooper N, Hollenberg PF (2011) Mechanism-based inactivation of human cytochrome P450 2B6 by clopidogrel: involvement of both covalent modification of cysteinyl residue 475 and loss of heme. Mol Pharmacol 80:839-847 https://doi.org/10.1124/mol.111.073783
  32. D'Agostino J, Zhang H, Kenaan C, Hollenberg PF (2015) Mechanism-based inactivation of human cytochrome P450 2B6 by chlorpyrifos. Chem Res Toxicol 28:1484-1495 https://doi.org/10.1021/acs.chemrestox.5b00156
  33. Cao J, Zheng L, Ji L, Lu D, Peng Y, Zheng J (2015) Mechanism-based inactivation of cytochrome P450 2B6 by isoimperatorin. Chem Biol Interact 226:23-29 https://doi.org/10.1016/j.cbi.2014.12.009