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

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作者
David André Barrière
Christophe Noll
Geneviève Roussy
Farah Lizotte
Anissa Kessai
Karyn Kirby
Karine Belleville
Nicolas Beaudet
Jean-Michel Longpré
André C. Carpentier
Pedro Geraldes
Philippe Sarret
机构
[1] Université de Sherbrooke,Département de Pharmacologie et Physiologie/Institut de Pharmacologie de Sherbrooke
[2] Service d’Endocrinologie,Département de Médecine
[3] Faculté de Médecine et des Sciences de la Santé,undefined
[4] Université de Sherbrooke,undefined
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Scientific Reports | / 8卷
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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 [18F]-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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