Depression of drug-metabolizing activity in the human liver by interferon-beta
- PMID: 8423043
Depression of drug-metabolizing activity in the human liver by interferon-beta
Abstract
The depressant effect of interferon beta on drug-metabolizing activity in the human liver was investigated. Seven patients with chronic hepatitis C were treated with interferon beta at doses of 3 x 10(6) to 9 x 10(6) IU/day for 8 wk. The activities of 7-methoxycoumarin O-demethylase and 7-ethoxycoumarin O-deethylase in specimens obtained by liver biopsy were examined before and after interferon treatment. Theophylline pharmacokinetics were also examined before and after interferon treatment. Interferon beta treatment reduced the activities of both O-dealkylases from 6.0 (100%) to 3.2 (53%) nmol/gm liver per minute and from 1.9 (100%) to 1.1 (58%) nmol/gm liver per minute, respectively (p < 0.05). The total body clearance of theophylline was also decreased (from 0.76 to 0.56 ml/kg/min; p < 0.05), and its elimination half-life was increased (from 8.4 to 11.7 hr; p < 0.05); however, the volume of distribution was not significantly affected. The magnitude of the decreases in enzyme activities and in theophylline clearance varied widely in individual patients and did not correlate with the dose of interferon administered. This study provides the first direct evidence that interferon beta can depress the activity of drug-metabolizing enzymes in the human liver.
Similar articles
-
Depression of drug metabolizing activity in the human liver by interferon-alpha.Eur J Clin Pharmacol. 1990;39(4):365-7. doi: 10.1007/BF00315411. Eur J Clin Pharmacol. 1990. PMID: 2076719
-
Phase II clinical trial of combined natural interferon-beta plus recombinant interferon-gamma treatment of chronic hepatitis B.Hepatogastroenterology. 1998 Nov-Dec;45(24):2282-94. Hepatogastroenterology. 1998. PMID: 9951911 Clinical Trial.
-
[Effect of pegylated interferon beta-1a therapy on the liver fibrosis in chronic hepatitis C: a semi-quantitative analysis].Zhonghua Yi Xue Za Zhi. 2008 Jan 8;88(2):96-100. Zhonghua Yi Xue Za Zhi. 2008. PMID: 18353212 Clinical Trial. Chinese.
-
NTP technical report on the toxicity studies of Dibutyl Phthalate (CAS No. 84-74-2) Administered in Feed to F344/N Rats and B6C3F1 Mice.Toxic Rep Ser. 1995 Apr;30:1-G5. Toxic Rep Ser. 1995. PMID: 12209194
-
Interferons in the management of viral hepatitis.Cytokines Cell Mol Ther. 1998 Dec;4(4):229-41. Cytokines Cell Mol Ther. 1998. PMID: 10068057 Review.
Cited by
-
CYP-mediated therapeutic protein-drug interactions: clinical findings, proposed mechanisms and regulatory implications.Clin Pharmacokinet. 2010 May;49(5):295-310. doi: 10.2165/11319980-000000000-00000. Clin Pharmacokinet. 2010. PMID: 20384392 Review.
-
Immunological response as a source to variability in drug metabolism and transport.Front Pharmacol. 2012 Feb 10;3:8. doi: 10.3389/fphar.2012.00008. eCollection 2012. Front Pharmacol. 2012. PMID: 22363283 Free PMC article.
-
Effect of tildrakizumab (MK-3222), a high affinity, selective anti-IL23p19 monoclonal antibody, on cytochrome P450 metabolism in subjects with moderate to severe psoriasis.Br J Clin Pharmacol. 2018 Oct;84(10):2292-2302. doi: 10.1111/bcp.13670. Epub 2018 Jul 31. Br J Clin Pharmacol. 2018. PMID: 29926968 Free PMC article. Clinical Trial.
-
Pertussis toxin-induced alterations of murine hepatic drug metabolism following administration of diphtheria and tetanus toxoids and pertussis vaccine adsorbed.Infect Immun. 1993 Oct;61(10):4240-7. doi: 10.1128/iai.61.10.4240-4247.1993. Infect Immun. 1993. PMID: 8406812 Free PMC article.
-
SARS-CoV-2-associated gastrointestinal and liver diseases: what is known and what is needed to explore.Egypt Liver J. 2021;11(1):64. doi: 10.1186/s43066-021-00123-6. Epub 2021 Jul 31. Egypt Liver J. 2021. PMID: 34777871 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources