TY - JOUR T1 - Macitentan Does Not Interfere with Hepatic Bile Salt Transport JF - Journal of Pharmacology and Experimental Therapeutics JO - J Pharmacol Exp Ther SP - 130 LP - 143 DO - 10.1124/jpet.114.214106 VL - 350 IS - 1 AU - Alexander Treiber AU - Päivi Äänismaa AU - Ruben de Kanter AU - Stephane Delahaye AU - Marianne Treher AU - Patrick Hess AU - Patricia Sidharta Y1 - 2014/07/01 UR - http://jpet.aspetjournals.org/content/350/1/130.abstract N2 - Treatment of pulmonary arterial hypertension with the endothelin receptor antagonist bosentan has been associated with transient increases in liver transaminases. Mechanistically, bosentan inhibits the bile salt export pump (BSEP) leading to an intrahepatic accumulation of cytotoxic bile salts, which eventually results in hepatocellular damage. BSEP inhibition by bosentan is amplified by its accumulation in the liver as bosentan is a substrate of organic anion-transporting polypeptide (OATP) transport proteins. The novel endothelin receptor antagonist macitentan shows a superior liver safety profile. Introduction of the less acidic sulfamide moiety and increased lipophilicity yield a hepatic disposition profile different from other endothelin receptor antagonists. Passive diffusion rather than OATP-mediated uptake is the driving force for macitentan uptake into the liver. Interaction with the sodium taurocholate cotransporting polypeptide and BSEP transport proteins involved in hepatic bile salt homeostasis is therefore limited due to the low intrahepatic drug concentrations. Evidence for this conclusion is provided by in vitro experiments in drug transporter-expressing cell lines, acute and long-term studies in rats and dogs, absence of plasma bile salt changes in healthy human volunteers after multiple dosing, and finally the liver safety profile of macitentan in the completed phase III morbidity/mortality SERAPHIN (Study with an Endothelin Receptor Antagonist in Pulmonary Arterial Hypertension to Improve Clinical Outcome) trial. ER -