We will test the hypothesis that the bioavailability of FK506 in stable renal transplant recipients, under steady state conditions, is largely determined by both enteric and hepatic P450 3A4 activity. Furthermore, the effect of the intestinal multi-drug resistance (mdr1) transporter on enteric metabolism and subsequent FK506 bioavailability will be examined. The underlying hypothesis is that interpatient variation in P450 3A4 and mdr1 expression largely accounts for interindividual differences in the oral clearance of FK506.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
3M01RR000042-39S1
Application #
6113517
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
39
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Type
DUNS #
791277940
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
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