Tissue-specific regulation of expression and activity of P-glycoprotein in adjuvant arthritis rats

Eur J Pharm Sci. 2002 Jul;16(1-2):29-36. doi: 10.1016/s0928-0987(02)00052-0.

Abstract

Cyclosporine A and steroids are effective against rheumatoid arthritis and also known as substrates of P-glycoprotein (P-gp). We investigated the effect of arthritis on the hepatic and intestinal P-gp activity in rats, and substantiated the expression level of the hepatic P-gp. Doxorubicin was used as a P-gp substrate. Cumulative biliary excretion and intestinal exsorption of doxorubicin following intravenous administration were compared between adjuvant arthritis (AA) and normal rats. Intestinal P-gp activity was also investigated by intestinal everted sac method, and hepatic P-gp was detected by FITC-labeled antibody and visualized using a confocal laser microscope system. Biliary clearance of doxorubicin in AA rats was significantly decreased from that in normal rats. The expression level of the hepatic P-gp in AA rats was very low compared to normal rats, indicating down-regulation. Intestinal exsorption clearance was not different between AA and normal rats. Permeability of doxorubicin across intestinal everted sac was comparable between AA and normal rats, corresponding to in vivo study. In AA rats, hepatic P-gp activity was decreased due to the reduction of expression level, but intestinal P-gp activity was not changed. Different regulation systems may be involved in liver and intestine.

Publication types

  • Comparative Study

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 1 / biosynthesis*
  • Animal Population Groups
  • Animals
  • Area Under Curve
  • Arthritis, Experimental / metabolism*
  • Bile / metabolism
  • Blood Proteins / metabolism
  • Chromatography, High Pressure Liquid
  • Doxorubicin / blood
  • Doxorubicin / pharmacokinetics*
  • Female
  • Half-Life
  • Injections, Intravenous
  • Intestinal Mucosa / metabolism
  • Intestines / drug effects
  • Liver / drug effects
  • Liver / metabolism
  • Organ Specificity
  • Protein Binding
  • Rats
  • Rats, Inbred Lew

Substances

  • ATP Binding Cassette Transporter, Subfamily B, Member 1
  • Blood Proteins
  • Doxorubicin