Alterations of hepatic microsomal enzymes in the early phase of murine schistosomiasis

Acta Trop. 2005 Jul;95(1):58-66. doi: 10.1016/j.actatropica.2005.04.013.

Abstract

Schistosoma mansoni has been reported to cause a downregulation of hepatic cytochrome P450 activities after granulomas are formed around worm eggs harbored in the mouse liver. Only a few studies, however, provided data on the activity of xenobiotic-biotransaformation enzymes in the early phase of S. mansoni infection. In this study, we evaluated the alterations of liver microsomal enzymes during early infection (post-infection days, PIDs, 15 and 30) when granulomas are not found in the mouse liver yet. Swiss Webster (SW) and DBA/2 mice of either sex were infected with 100 S. mansoni cercariae on postnatal day 10. Levels of total-CYPs and activities of alkoxyresorufin-O-dealkylases (EROD, MROD, PROD and BROD), N-nitrosodimethylamine-N-demethylase (NDMA-d), coumarin 7-hydroxylase (COH, DBA/2 only) and UDP-glucuronosyltransferase (UGT) were measured in liver microsomes from mice killed on PIDs 15 and 30. Age-matched (sham-infected) mice of the same sex and strain were used as controls. Neither total-CYP levels nor microsomal enzyme activities were altered in SW and DBA/2 mice on PID 15. On PID 30, total-CYP levels, and COH, PROD and UGT activities remained unaltered, while gender- and strain-specific minor changes of EROD, MROD, BROD and NDMA-d (i.e., increase in SW and reduction in DBA/2) were found. In conclusion, our results suggest that, contrasting to a consistent and almost generalized downregulation of CYPs in chronic schistosomiasis, alterations of hepatic CYPs in early (acute) infection are isoform and mouse's gender and strain specific.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Animals
  • Cytochrome P-450 Enzyme System / metabolism
  • Female
  • Glucuronosyltransferase / metabolism
  • Isoenzymes / metabolism
  • Male
  • Mice
  • Mice, Inbred DBA
  • Microsomes, Liver / enzymology*
  • Microsomes, Liver / pathology
  • Schistosoma mansoni / pathogenicity*
  • Schistosomiasis mansoni / parasitology
  • Schistosomiasis mansoni / physiopathology*
  • Time Factors

Substances

  • Isoenzymes
  • Cytochrome P-450 Enzyme System
  • Glucuronosyltransferase