Intestinal OATP1A2 inhibition as a potential mechanism for the effect of grapefruit juice on aliskiren pharmacokinetics in healthy subjects

Eur J Clin Pharmacol. 2012 May;68(5):697-708. doi: 10.1007/s00228-011-1167-4. Epub 2011 Nov 29.

Abstract

Purpose: To conduct a mechanistic investigation of the interaction between aliskiren and grapefruit juice in healthy subjects.

Methods: Twenty-eight subjects received an oral dose of aliskiren 300 mg (highest recommended clinical dose) with 300 mL of either water or grapefruit juice in a two-way crossover design. Safety and pharmacokinetic analyses were performed. In vitro studies were performed in HEK293 cells to investigate the role of organic anion transporting polypeptide (OATP) transporter-mediated uptake of aliskiren.

Results: Co-administration of a single dose of aliskiren with grapefruit juice decreased the plasma concentration of aliskiren, with mean decreases in the AUC(inf), AUC(last), and C(max) of 38, 37, and 61%, respectively. The uptake of [¹⁴C]aliskiren into OATP2B1-expressing cells was essentially the same as that into control cells, and the inhibitor combination atorvastatin and rifamycin had no effect on [¹⁴C]aliskiren accumulation in either cell type. The uptake of [¹⁴C]aliskiren and [³H]fexofenadine was linear in OATP1A2-expressing cells and was reduced by naringin, with IC₅₀ values of 75.5 ± 11.6 and 24.2 ± 2.0 μM, respectively.

Conclusions: Grapefruit juice decreases exposure of aliskiren partially via inhibition of intestinal OATP1A2.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amides / adverse effects
  • Amides / blood
  • Amides / metabolism
  • Amides / pharmacokinetics*
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / blood
  • Antihypertensive Agents / metabolism
  • Antihypertensive Agents / pharmacokinetics*
  • Beverages / adverse effects*
  • Beverages / analysis
  • Biological Transport / drug effects
  • Citrus paradisi / chemistry*
  • Cross-Over Studies
  • Flavanones / analysis
  • Flavanones / pharmacology
  • Food-Drug Interactions*
  • Fruit / chemistry
  • Fumarates / adverse effects
  • Fumarates / blood
  • Fumarates / metabolism
  • Fumarates / pharmacokinetics*
  • HEK293 Cells
  • Half-Life
  • Humans
  • Intestinal Mucosa / enzymology*
  • Male
  • Organic Anion Transporters / antagonists & inhibitors*
  • Organic Anion Transporters / genetics
  • Organic Anion Transporters / metabolism
  • Recombinant Proteins / antagonists & inhibitors
  • Recombinant Proteins / metabolism
  • Renin / antagonists & inhibitors
  • Terfenadine / analogs & derivatives
  • Terfenadine / metabolism
  • Young Adult

Substances

  • Amides
  • Antihypertensive Agents
  • Flavanones
  • Fumarates
  • Organic Anion Transporters
  • Recombinant Proteins
  • SLCO1A2 protein, human
  • aliskiren
  • Terfenadine
  • fexofenadine
  • Renin
  • naringin