@article {Johns227, author = {Douglas G. Johns and Lauretta LeVoci and Mihajlo Krsmanovic and Min Lu and Georgy Hartmann and Suoyu Xu and Sheng-Ping Wang and Ying Chen and Thomas Bateman and Robert O. Blaustein}, title = {Characterization of Anacetrapib Distribution into the Lipid Droplet of Adipose Tissue in Mice and Human Cultured Adipocytes}, volume = {47}, number = {3}, pages = {227--233}, year = {2019}, doi = {10.1124/dmd.118.084525}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {Anacetrapib is an inhibitor of cholesteryl ester transfer protein (CETP), associated with reduction in LDL cholesterol and increase in HDL cholesterol in hypercholesterolemic patients. Anacetrapib was not taken forward into filing/registration as a new drug for coronary artery diease, despite the observation of a \~{}9\% reduction in cardiovascular risk in a large phase III cardiovascular outcomes trial (REVEAL). Anacetrapib displayed no adverse effects throughout extensive preclinical safety evaluation, and no major safety signals were observed in clinical trials studying anacetrapib, including REVEAL. However, anacetrapib demonstrated a long terminal half-life in all species, thought to be due, in part, to distribution into adipose tissue. We sought to understand the dependence of anacetrapib{\textquoteright}s long half-life on adipose tissue and to explore potential mechanisms that might contribute to the phenomenon. In mice, anacetrapib localized primarily to the lipid droplet of adipocytes in white adipose tissue; in vitro, anacetrapib entry into cultured human adipocytes depended on the presence of a mature adipocyte and lipid droplet but did not require active transport. In vivo, the entry of anacetrapib into adipose tissue did not require lipase activity, as the distribution of anacetrapib into adipose was-not affected by systemic lipase inhibition using poloaxamer-407, a systemic lipase inhibitor. The data from these studies support the notion that the entry of anacetrapib into adipose tissue/lipid droplets does not require active transport, nor does it require mobilization or entry of fat into adipose via lipolysis.}, issn = {0090-9556}, URL = {https://dmd.aspetjournals.org/content/47/3/227}, eprint = {https://dmd.aspetjournals.org/content/47/3/227.full.pdf}, journal = {Drug Metabolism and Disposition} }