PT - JOURNAL ARTICLE AU - Jill S. Warrington AU - David J. Greenblatt AU - Lisa L. von Moltke TI - The Effect of Age on P-Glycoprotein Expression and Function in the Fischer-344 Rat AID - 10.1124/jpet.103.061234 DP - 2004 May 01 TA - Journal of Pharmacology and Experimental Therapeutics PG - 730--736 VI - 309 IP - 2 4099 - http://jpet.aspetjournals.org/content/309/2/730.short 4100 - http://jpet.aspetjournals.org/content/309/2/730.full SO - J Pharmacol Exp Ther2004 May 01; 309 AB - We investigated the effect of age on P-glycoprotein (P-gp) expression and function in rat liver, intestine, kidney, and endothelial cells of the blood-brain barrier (BBB) and lymphocytes. Flow cytometric analysis was used to examine P-gp expression in lymphocytes from male Fischer-344 rats from three age groups (young at 3-4 months, intermediate at 13-14 months, and old at 25-26 months). In addition, P-gp function in lymphocytes was assessed by measuring the ability of the P-gp inhibitor verapamil to limit the efflux of the fluorescent P-gp substrate rhodamine 123. P-gp expression was evaluated in the remaining four tissues by Western blot analysis. The effect of age on P-gp expression was tissue-specific. Although lymphocytic and hepatic P-gp expression increased with age, renal P-gp content was lower in the old kidneys. No statistical difference was observed in P-gp expression in intestinal microsomes or in BBB cell lysates among the three age groups. P-gp function was also increased by 6- to 8-fold in lymphocytes from the old rats. When P-gp expression was compared with CYP3A expression in these rats (reported elsewhere in this journal), we found that P-gp expression increased with age, whereas CYP3A expression and activity declined in the old livers. The converse pattern was observed in the kidney. Thus, age-related changes in P-gp expression and function are likely to be tissue-specific, and these changes may be inversely related to differences in CYP3A expression. The American Society for Pharmacology and Experimental Therapeutics