Total gastrectomy may result in reduced drug effectiveness due to an increase in the expression of the drug-metabolizing enzyme Cytochrome P450, in the liver

Eur J Pharm Sci. 2014 Jan 23:51:180-8. doi: 10.1016/j.ejps.2013.09.017. Epub 2013 Oct 3.

Abstract

In patients with gastrectomy, it is possible that drug effectiveness is reduced compared to healthy subjects due to the increased of the drug-metabolizing enzyme, Cytochrome P450 (CYP). The purpose of this study is to verify this possibility. Gastrectomy model mice were prepared to evaluate the expression level of various CYPs in the liver from 2 to 24 weeks post-operation. No significant differences were observed in the protein expression levels of CYP3A, CYP1A, CYP2C, and CYP2D between the sham operation group and the gastrectomy group up to 4 weeks after the gastrectomy. On the other hand, significant increases in the protein expression levels of any CYPs were observed in the gastrectomy group compared to the sham operation group from 12 weeks after the gastrectomy onward. These increases in expression levels were maintained until 24 weeks after the gastrectomy. The examination of metabolic activity in the liver in the gastrectomy group using triazolam revealed that the metabolic activity at 12 weeks after the gastrectomy was significantly increased in the gastrectomy group. The administration of the anticancer drug imatinib, which is a substrate of CYP3A, to mice at 12weeks after gastrectomy resulted in an increase in the metabolic rate, suggesting a possible decrease in drug effectiveness. It has been revealed that drug effectiveness may be reduced after gastrectomy because the expression levels of various CYPs in the liver were increased over a prolonged period. The results of this study can serve as valuable fundamental knowledge for drug therapy in patients with gastrectomy.

Keywords: Cytochrome P450; Gastrectomy; Imatinib.

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / metabolism
  • Animals
  • Basal Metabolism / drug effects
  • Basal Metabolism / physiology
  • Benzamides / pharmacology
  • Body Weight / drug effects
  • Body Weight / genetics
  • Cytochrome P-450 Enzyme System / metabolism*
  • Eating / drug effects
  • Eating / physiology
  • Gastrectomy / adverse effects*
  • Imatinib Mesylate
  • Intestine, Large / drug effects
  • Intestine, Large / enzymology
  • Intestine, Large / metabolism
  • Intestine, Small / drug effects
  • Intestine, Small / enzymology
  • Intestine, Small / metabolism
  • Liver / drug effects
  • Liver / enzymology*
  • Liver / metabolism*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / enzymology
  • Microsomes, Liver / metabolism
  • Piperazines / pharmacology
  • Pyrimidines / pharmacology
  • Triazolam / metabolism

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Benzamides
  • Piperazines
  • Pyrimidines
  • Triazolam
  • Imatinib Mesylate
  • Cytochrome P-450 Enzyme System