Article Detail

Home > Article Detail
  • P-ISSN 1010-0695
  • E-ISSN 2288-3339

Sub-acute toxicity and effect of Hwangryunhaedok-tang on human drug-metabolizing enzymes

Journal of Korean Medicine / Journal of Korean Medicine, (P)1010-0695; (E)2288-3339
2017, v.38 no.2, pp.15-30
https://doi.org/10.13048/jkm.17014






  • Downloaded
  • Viewed

Abstract

Objectives: Hwangryunhaedok-tang (HHT; Huanglianjiedu-tang, Orengedoku-to), a traditional herbal formula, is used for treating inflammation, hypertension, gastritis, liver dysfunction, cerebrovascular diseases, dermatitis and dementia. The objective of this study was to assess the sub-acute toxicity of HHT in Sprague-Dawley (SD) rats, and its effect on the activities of human microsomal cytochrome P450s (CYP450s) and UDP-glucuronosyltransferases (UGTs). Methods: Male and female SD rats were orally administered HHT once daily at doses of 0, 500, 1000 and 2000 mg/kg for 4 weeks. We analyzed mortality, clinical observations, body weight, food consumption, organ weights, urinalysis, hematology, serum biochemistry, and histopathology. The activities of major human CYP450s (CYP1A2, CYP3A4, CYP2B6, CYP2C9, CYP2C19, CYP2D6, and CYP2E1) and UGTs (UGT1A1, UGT1A4, and UGT2B7) were assessed using in vitro fluorescence- and luminescence-based enzyme assays, respectively. Results: No toxicologically significant changes related to the repeated administration of HHT were observed in both male and female SD rats. The no observed adverse effect level (NOAEL) value was more than 2000 mg/kg/day for both sexes. HHT inhibited the activities of human microsomal CYP1A2, CYP2C19, CYP2D6, and CYP2E1, whereas it weakly inhibited the activities of CYP2B6, CYP2C9, CYP3A4, and UGT1A1. In addition, HHT negligibly inhibited the activities of human microsomal UGT1A4 and UGT2B7 with IC50 values in excess of 1000 μg/mL. Conclusions: Our findings indicate that HHT may be safe for repeated administration up to 4 weeks. In addition, these findings provide information on the safety and effectiveness of HHT when co-administered with conventional drugs.

keywords
Hwangryunhaedok-tang, sub-acute toxicity, cytochrome P450, UDP-glucuronosyltransferase, herb-drug interactions


Reference

1

1. Firenzuoli F, Gori L. Herbal medicine today:clinical and research issues. Evid Based Complement Alternat Med. 2007;4(Suppl 1):37-40.

2

2. Moreira DL, Teixeira SS, Monteiro MHD, De-Oliveira ACAX, Paumgartten FJR. Traditional use and safety of herbal medicines. Revista Brasileira de Farmacognosia. 2014;24(2):248-57.

3

3. Nebert DW, Russell DW. Clinical importance of the cytochromes P450. Lancet. 2002;360(9340):1155-62.

4

4. Wienkers LC, Heath TG. Predicting in vivo drug interactions from in vitro drug discovery data. Nat Rev Drug Discov. 2005;4(10):825-33.

5

5. Court MH, Hazarika S, Krishnaswamy S, Finel M, Williams JA. Novel polymorphic human UDP-glucuronosyltransferase 2A3: cloning, functional characterization of enzyme variants, comparative tissue expression, and gene induction. Mol Pharmacol. 2008;74(3):744-54.

6

6. Mackenzie PI, Bock KW, Burchell B, Guillemette C, Ikushiro S, Iyanagi T, et al. Nomenclature update for the mammalian UDP glycosyltransferase (UGT) gene superfamily. Pharmacogenet Genomics. 2005;15(10):677-85.

7

7. Hur J. Donguibogam. Seoul:Namsandang. 2007:382.

8

8. Lu J, Wang JS, Kong LY. Anti-inflammatory effects of Huang-Lian-Jie-Du decoction, its two fractions and four typical compounds. J Ethnopharmacol. 2011;134(3):911-8.

9

9. Ohta Y, Kongo-Nishimura M, Hayashi T, Kishikawa T. Effect of Oren-gedoku-to (Huanglian -Jie-Du-Tang) extract on disruption of hepatic antioxidant defense systems in rats treated with D-galactosamine. J Ethnopharmacol. 2004;94(2-3):323-9.

10

10. Lee MY, Seo CS, Kim YB, Shin IS, Shin HK. Non-clinical safety assessment of Hwangryunhaedok -tang: 13-week toxicity in Crl:CD Sprague Dawley rats. Regul Toxicol Pharmacol. 2014;68(3):378-86.

11

11. Seo CS, Kim OS, Kim JH, Shin HK. Simultaneous quantification and antiatherosclerosis effect of the traditional Korean medicine, Hwangryunhaedok-tang. BMC Complement Altern Med. 2015;15:108.

12

12. Jin SE, Seo CS, Shin HK, Ha H. Traditional Herbal Formulas to as Treatments for Musculoskeletal Disorders: Their Inhibitory Effects on the Activities of Human Microsomal Cytochrome P450s and UDP-glucuronosyltransferases. Pharmacogn Mag. 2016;12(48):241-52.

13

13. Raymond JR, Yarger WE. Abnormal urine color: differential diagnosis. South Med J. 1988;81(7):837-41.

14

14. Lee YC, Lee JN, Bae JS, Park YC. Green urine in a patient who received a continuous infusion of propofol. Kor J Anesthesiol. 2009;56:325-7.

15

15. Gonzalez Frank J, Tukey Robert H. Chapter 3, Drug metabolism. In: Brunton LL, Lazo JS, Parker KL. Goodman & Gilman’s the pharmacological basis of therapeutics, 11th ed. New York:McGraw Hill. 2006:71-91.

16

16. Wang BL, Li Y. Progress of pharmacokinetic interactions and possible mechanisms of botanical medicines-chemical drugs. Chin J Pharmacol Toxicol. 2008;22:237-40.

17

17. Flockhart DA, Oesterheld JR. Cytochrome P450-mediated drug interactions. Child Adolesc Psychiatr Clin N Am. 2000;9(1):43-76.

18

18. Bush TM, Rayburn KS, Holloway SW, Sanchez-Yamamoto DS, Allen BL, Lam T, et al. Adverse interactions between herbal and dietary substances and prescription medications:a clinical survey. Altern Ther Health Med. 2007;13(2):30-5.

19

19. Lee SY, Jang H, Lee JY, Ma JY, Oh SJ, Kim SK. Inhibitory effects of Hwang-Ryun-Hae-Dok -Tang on cytochrome P450 in human liver microsomes. Xenobiotica. 2015;45(2):131-8.

20

20. Katoh M, Yoshioka Y, Nakagawa N, Yokoi T. Effects of Japanese herbal medicine, Kampo, on human UGT1A1 activity. Drug Metab Pharmacokinet. 2009;24(3):226-34.

21

21. Kang JJ, Chen YC, Kuo WC, Chen T, Cheng YW, Kuo ML, et al. Modulation of microsomal cytochrome P450 by Scutellariae Radix and Gentianae scabrae Radix in rat liver. Am J Chin Med. 1996;24(1):19-29.

22

22. Ma T, Huang C, Zong G, Zha D, Meng X, Li J, et al. Hepatoprotective effects of geniposide in a rat model of nonalcoholic steatohepatitis. J Pharm Pharmacol. 2011;63(4):587-93.

23

23. Guo Y, Chen Y, Tan ZR, Klaassen CD, Zhou HH. Repeated administration of berberine inhibits cytochromes P450 in humans. Eur J Clin Pharmacol. 2012;68(2):213-7.

24

24. Vrba J, Papouskova B, Pyszkova M, Zatloukalova M, Lemr K, Ulrichova J, et al. Metabolism of palmatine by human hepatocytes and recombinant cytochromes P450. J Pharm Biomed Anal. 2015;102:193-8.

25

25. Ogu CC, Maxa JL. Drug interactions due to cytochrome P450. Proc (Bayl Univ Med Cent). 2000;13(4):421-3.

26

26. Marino MR, Vachharajani NN. Drug interactions with irbesartan. Clin Pharmacokinet. 2001;40(8):605-14.

상단으로 이동

Journal of Korean Medicine