Atherosclerosis · 2014
Raising HDL with CETP inhibitor torcetrapib improves glucose homeostasis in dyslipidemic and insulin resistant hamsters.
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Briand François, Prunet-Marcassus Bénédicte, Thieblemont Quentin, Costard Clément, Muzotte Elodie, Sordello Sylvie, Sulpice Thierry
Аннотация
We investigated whether raising HDL-cholesterol levels with cholesteryl ester transfer protein (CETP) inhibition improves glucose homeostasis in dyslipidemic and insulin resistant hamsters. Compared with vehicle, torcetrapib 30 mg/kg/day (TOR) administered for 10 days significantly increased by ∼40% both HDL-cholesterol levels and 3H-tracer appearance in HDL after 3H-cholesterol labeled macrophages i.p. injection. TOR significantly reduced fasting plasma triglycerides, glycerol and free fatty acids levels by 65%, 31% and 23%, respectively. TOR also reduced blood glucose levels and plasma insulin by 20% and 49% respectively, which led to a 60% reduction in HOMA-IR index (all p<0.01). After 3H-2-deoxyglucose and insulin injection, TOR significantly increased glucose uptake in oxidative soleus muscle, liver and heart by 26, 33 and 70%, respectively. Raising HDL levels with the CETP inhibitor torcetrapib improves glucose homeostasis in dyslipidemic and insulin resistant hamsters. Whether similar effect would be observed with other CETP inhibitors should be investigated.
Предметные рубрики MeSH
AMP-Activated Protein KinasesAnimalsAnticholesteremic AgentsApolipoprotein A-IApolipoproteins ECholesterol Ester Transfer ProteinsCholesterol, HDLCricetinaeDeoxyglucoseDiet, AtherogenicDisease Models, AnimalDrug Evaluation, PreclinicalDyslipidemiasEnzyme ActivationFecesGlucoseHomeostasisHyperglycemiaInsulin ResistanceMaleMesocricetusMuscle, SkeletalQuinolinesRandom AllocationSpecies Specificity