Intracellular sirolimus concentration is reduced by tacrolimus in human pancreatic islets in vitro

Transpl Int. 2015 Oct;28(10):1152-61. doi: 10.1111/tri.12617. Epub 2015 Jun 23.

Abstract

Main problem: Islet transplantation has become a promising treatment for type 1 diabetes. However, immunosuppressive drugs used today cause islet deterioration and modification strategies are necessary. But little is known about pharmacokinetics interactions and intracellular concentrations of immunosuppressive drugs in human islets.

Methods: We determined the pharmacokinetics of tacrolimus and sirolimus in islets by measuring intracellular concentration after exposure alone or in combination at two different doses up to 48 h. A quantification technique established in our laboratory using a Micromass Quattro micro API MS/MS-instrument with electrospray ionization was used. Islets function was measured by oxygen consumption rates. Presence of drug transporters OATP1B1 and ABCB1 and metabolizing enzyme CYP3A4 in islets were quantified using real-time quantitative PCR.

Results: Islets incubated with tacrolimus and sirolimus had a significant decrease in intracellular concentration of sirolimus compared to sirolimus alone. Reduced intracellular sirolimus concentration was followed by increased p70S6k phosphorylation suggesting preservation of the mTOR-signaling pathway. Drug transporters OATP1B1 and ABCB1 and enzyme CYP3A4 were expressed in human islets, but were not involved in the reduced sirolimus concentration by tacrolimus.

Conclusion: These findings provide new knowledge of the drug interaction between tacrolimus and sirolimus, suggesting that tacrolimus has an inhibitory effect on the intracellular concentration of sirolimus in human islets.

Keywords: diabetes; human islets; immunosuppressive drugs; intracellular drug concentration; sirolimus; tacrolimus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / metabolism
  • Adult
  • Aged
  • Biological Transport / drug effects
  • Cells, Cultured
  • Cyclosporine / pharmacology
  • Cytochrome P-450 CYP3A / metabolism
  • Drug Interactions
  • Glucose / pharmacology
  • Humans
  • Immunosuppressive Agents / metabolism*
  • Immunosuppressive Agents / pharmacology
  • Islets of Langerhans / cytology
  • Islets of Langerhans / drug effects
  • Islets of Langerhans / metabolism*
  • Liver-Specific Organic Anion Transporter 1
  • Middle Aged
  • Organic Anion Transporters / metabolism
  • Osmolar Concentration
  • Oxygen Consumption / drug effects
  • Phosphorylation / drug effects
  • Protein Processing, Post-Translational / drug effects
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Sirolimus / metabolism*
  • TOR Serine-Threonine Kinases / metabolism
  • Tacrolimus / metabolism
  • Tacrolimus / pharmacology*
  • Young Adult

Substances

  • ABCB1 protein, human
  • ATP Binding Cassette Transporter, Subfamily B
  • Immunosuppressive Agents
  • Liver-Specific Organic Anion Transporter 1
  • Organic Anion Transporters
  • SLCO1B1 protein, human
  • Cyclosporine
  • Cytochrome P-450 CYP3A
  • CYP3A4 protein, human
  • MTOR protein, human
  • Ribosomal Protein S6 Kinases, 70-kDa
  • TOR Serine-Threonine Kinases
  • Glucose
  • Sirolimus
  • Tacrolimus