Can Bile Salt Export Pump Inhibition Testing in Drug Discovery and Development Reduce Liver Injury Risk? An International Transporter Consortium Perspective

Clin Pharmacol Ther. 2018 Nov;104(5):916-932. doi: 10.1002/cpt.1222.

Abstract

Bile salt export pump (BSEP) inhibition has emerged as an important mechanism that may contribute to the initiation of human drug-induced liver injury (DILI). Proactive evaluation and understanding of BSEP inhibition is recommended in drug discovery and development to aid internal decision making on DILI risk. BSEP inhibition can be quantified using in vitro assays. When interpreting assay data, it is important to consider in vivo drug exposure. Currently, this can be undertaken most effectively by consideration of total plasma steady state drug concentrations (Css,plasma ). However, because total drug concentrations are not predictive of pharmacological effect, the relationship between total exposure and BSEP inhibition is not causal. Various follow-up studies can aid interpretation of in vitro BSEP inhibition data and may be undertaken on a case-by-case basis. BSEP inhibition is one of several mechanisms by which drugs may cause DILI, therefore, it should be considered alongside other mechanisms when evaluating possible DILI risk.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B, Member 11 / antagonists & inhibitors*
  • ATP Binding Cassette Transporter, Subfamily B, Member 11 / chemistry
  • ATP Binding Cassette Transporter, Subfamily B, Member 11 / genetics
  • ATP Binding Cassette Transporter, Subfamily B, Member 11 / metabolism
  • Animals
  • Bile / metabolism*
  • Cells, Cultured
  • Chemical and Drug Induced Liver Injury / etiology*
  • Chemical and Drug Induced Liver Injury / genetics
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / prevention & control
  • Computer Simulation
  • Computer-Aided Design
  • Drug Design
  • Drug Development / methods*
  • Drug Discovery / methods*
  • Humans
  • In Vitro Techniques
  • Liver / drug effects*
  • Liver / metabolism
  • Membrane Transport Modulators / chemistry
  • Membrane Transport Modulators / toxicity*
  • Models, Biological
  • Protein Conformation
  • Risk Assessment
  • Risk Factors
  • Structure-Activity Relationship

Substances

  • ABCB11 protein, human
  • ATP Binding Cassette Transporter, Subfamily B, Member 11
  • Membrane Transport Modulators