Combination of high-fat/high-fructose diet and low-dose streptozotocin to model long-term type-2 diabetes complications

David André Barrière(Université de Sherbrooke), Christophe Noll(Université de Sherbrooke), Geneviève Roussy(Université de Sherbrooke), Farah Lizotte(Université de Sherbrooke), Anissa Kessai(Université de Sherbrooke), Karyn Kirby(Université de Sherbrooke), Karine Belleville(Université de Sherbrooke), Nicolas Beaudet(Université de Sherbrooke), Jean‐Michel Longpré(Université de Sherbrooke), André C. Carpentier(Université de Sherbrooke), Pedro Geraldes(Université de Sherbrooke), Philippe Sarret(Université de Sherbrooke)
Scientific Reports
January 5, 2018
Cited by 167Open Access
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Abstract

Abstract The epidemic of type 2 diabetes mellitus (T2DM) is fueled by added fructose consumption. Here, we thus combined high-fat/high-fructose diet, with multiple low-dose injections of streptozotocin (HF/HF/Stz) to emulate the long-term complications of T2DM. HF/HF/Stz rats, monitored over 56 weeks, exhibited metabolic dysfunctions associated with the different stages of the T2DM disease progression in humans: an early prediabetic phase characterized by an hyperinsulinemic period with modest dysglycemia, followed by a late stage of T2DM with frank hyperglycemia, normalization of insulinemia, marked dyslipidemia, hepatic fibrosis and pancreatic β-cell failure. Histopathological analyses combined to [ 18 F]-FDG PET imaging further demonstrated the presence of several end-organ long-term complications, including reduction in myocardial glucose utilization, renal dysfunction as well as microvascular neuropathy and retinopathy. We also provide for the first time a comprehensive µ-PET whole brain imaging of the changes in glucose metabolic activity within discrete cerebral regions in HF/HF/Stz diabetic rats. Altogether, we developed and characterized a unique non-genetic preclinical model of T2DM adapted to the current diet and lifestyle that recapitulates the major metabolic features of the disease progression, from insulin resistance to pancreatic β-cell dysfunction, and closely mimicking the target-organ damage occurring in type 2 diabetic patients at advanced stages.


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