Are cytochrome P450 3A enzymes in the small intestine responsible for different cyclosporine metabolite patterns in stable male and female renal allograft recipients after co-administration of diltiazem?

Transplant Proc. 1996 Aug;28(4):2159-61.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Calcium Channel Blockers / pharmacology*
  • Cyclosporine / metabolism*
  • Cyclosporine / pharmacokinetics
  • Cyclosporine / therapeutic use
  • Cytochrome P-450 CYP2E1
  • Cytochrome P-450 Enzyme System / metabolism*
  • Diltiazem / pharmacology*
  • Duodenum
  • Female
  • Humans
  • Immunosuppressive Agents / metabolism*
  • Immunosuppressive Agents / pharmacokinetics
  • Immunosuppressive Agents / therapeutic use
  • Intestinal Mucosa / enzymology*
  • Kidney Transplantation* / immunology
  • Male
  • Metabolic Clearance Rate
  • Microsomes / enzymology
  • Middle Aged
  • Mixed Function Oxygenases / metabolism*
  • Sex Characteristics

Substances

  • Calcium Channel Blockers
  • Immunosuppressive Agents
  • Cyclosporine
  • Cytochrome P-450 Enzyme System
  • Mixed Function Oxygenases
  • Cytochrome P-450 CYP2E1
  • Diltiazem