Novel canine models of obese prediabetes and mild type 2 diabetes

作者：Ionut Viorica^*; Liu Huiwen; Mooradian Vahe; Castro Ana Valeria B; Kabir Morvarid; Stefanovski Darko; Zheng Dan; Kirkman Erlinda L; Bergman Richard N

来源：American Journal of Physiology - Endocrinology And Metabolism, 2010, 298(1): E38-E48.

DOI：10.1152/ajpendo.00466.2009

• obesity
• animal models
• streptozotocin
• insulin secretion

Ionut V, Liu H, Mooradian V, Castro AV, Kabir M, Stefanovski D, Zheng D, Kirkman EL, Bergman RN. Novel canine models of obese prediabetes and mild type 2 diabetes. Am J Physiol Endocrinol Metab 298: E38-E48, 2010. First published October 20, 2009; doi: 10.1152/ajpendo.00466.2009.-Human type 2 diabetes mellitus (T2DM) is often characterized by obesity-associated insulin resistance (IR) and beta-cell function deficiency. Development of relevant large animal models to study T2DM is important and timely, because most existing models have dramatic reductions in pancreatic function and no associated obesity and IR, features that resemble more T1DM than T2DM. Our goal was to create a canine model of T2DM in which obesity-associated IR occurs first, followed by moderate reduction in beta-cell function, leading to mild diabetes or impaired glucose tolerance. Lean dogs (n = 12) received a high-fat diet that increased visceral (52%, P < 0.001) and subcutaneous (130%, P < 0.001) fat and resulted in a 31% reduction in insulin sensitivity (SI) (5.8 +/- 0.7 x 10(-4) to 4.1 +/- 0.5 x 10(-4) mu U.ml(-1).min(-1), P < 0.05). Animals then received a single low dose of streptozotocin (STZ; range 30-15 mg/kg). The decrease in beta-cell function was dose dependent and resulted in three diabetes models: 1) frank hyperglycemia (high STZ dose); 2) mild T2DM with normal or impaired fasting glucose (FG), 2-h glucose > 200 mg/dl during OGTT and 77-93% AIR(g) reduction (intermediate dose); and 3) prediabetes with normal FG, normal 2-h glucose during OGTT and 17-74% AIRg reduction (low dose). Twelve weeks after STZ, animals without frank diabetes had 58% more body fat, decreased beta-cell 17-93%), and 40% lower SI. We conclude that high-fat feeding and variable-dose STZ in dog result in stable models of obesity, insulin resistance, and 1) overt diabetes, 2) mild T2DM, or 3) impaired glucose tolerance. These models open new avenues for studying the mechanism of compensatory changes that occur in T2DM and for evaluating new therapeutic strategies to prevent progression or to treat overt diabetes.

• 出版日期2010-1