![]() | Only 14 pages are availabe for public view |
Abstract AIM OF THE WORK Diabetes mellitus is a risk factor for early complications and mortality in patients with peripheral artery disease. Apolipoprotein AI is also suggested to be a marker of increased cardiovascular risk. The coronary artery disease is associated with more than threefold-increased risk in diabetes mellitus. HDL and apo AI, a specific protein of this lipoprotein are risk factors for atherosclerosis. We were investigated the association and interaction between diabetes mellitus, Apo AI gene expression , Apo AI plasma levels and some atherogenic agents . For this purpose, two rat models for these pathologies have been established: a type I diabetic model obtained by streptozotocin injection to rat (STZ-diabetic), followed or not by insulin treatment (experiment 1); a type II diabetic model by feeding rat with a fructose riched diet (F-diabetic), followed or not by rosiglitazone treatment (experiment 2). This was occurred through study the effect of insulin and rosiglitazone –treatment on: 1.Gene expression of Apo AI in liver tissues . 2.Plasma Apo AI concentration. 3-Heart and liver tissues glycogen. 4- Blood glucose. |