Heart Uptake of [ 18 F]Fluoro-4-Thia-Oleate in a Non-Alcoholic Fatty Liver Disease Mouse Model.

The world-wide high incidence of non-alcoholic fatty liver disease (NAFLD) is of concern for its progression to insulin resistance, steatohepatitis and cardiovascular disease (CVD). The increased uptake of fatty acids in critical organs plays a major role in NAFLD progression. Male Ceacam1 -/- mice that develop NAFLD, insulin resistance and CVD on normal chow are a potential model for studying the dysregulation of fatty acid uptake. [ 18 F]fluoro-4-thia-oleate ([ 18 F]FTO) was chosen as a fatty acid reporter because of its higher uptake and retention in the heart in an animal model of CVD. Male wild-type (WT) or Ceacam1 -/- mice fasted 4-6 h were administered [ 18 F]FTO i.v., and dynamic PET scans were conducted in an MR/PET small animal imaging system along with terminal tissue biodistributions. Quantitative heart image analysis revealed significantly higher uptake at 35 min in Ceacam1 -/ - (6.0 ± 1.0% ID/cc) vs. WT (3.9 ± 0.6% ID/cc) mice ( p = 0.006). Ex vivo heart uptake/retention (% ID/organ) was 2.82 ± 0.45 for Ceacam1 -/ - mice vs. 1.66 ± 0.45 for WT mice ( p < 0.01). Higher kidney and pancreas uptake/retention in Ceacam1 -/ - was also evident, and the excretion of [ 18 F]FTO into the duodenum was observed for both WT and Ceacam1 -/ - mice starting at 10 min. This study suggests that the administration of [ 18 F]FTO as a marker of fatty acid uptake and retention may be an important tool in analyzing the effect of NAFLD on lipid dysregulation in the heart.