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首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >High fat diet-induced hyperglycemia: prevention by low level expression of a glucose transporter (GLUT4) minigene in transgenic mice.
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High fat diet-induced hyperglycemia: prevention by low level expression of a glucose transporter (GLUT4) minigene in transgenic mice.

机译:高脂饮食诱发的高血糖症:通过在转基因小鼠中低水平表达葡萄糖转运蛋白(GLUT4)来预防。

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摘要

High-fat intake leading to obesity contributes to the development of non-insulin-dependent diabetes mellitus (NIDDM, type 2). Similarly, mice fed a high-fat (safflower oil) diet develop defective glycemic control, hyperglycemia, and obesity. To assess the effect of a modest increase in the expression of GLUT4 (the insulin-responsive glucose transporter) on impaired glycemic control caused by fat feeding, transgenic mice harboring a GLUT4 minigene were fed a high-fat diet. Low-level tissue-specific (heart, skeletal muscle, and adipose tissue) expression of the GLUT4 minigene in transgenic mice prevented the impairment of glycemic control and accompanying hyperglycemia, but not obesity, caused by fat feeding. Thus, a small increase (< or = 2-fold) in the tissue level of GLUT4 prevents a primary symptom of the diabetic state in a mouse model, suggesting a possible target for intervention in the treatment of NIDDM.
机译:高脂摄入会导致肥胖,导致非胰岛素依赖型糖尿病(NIDDM,2型)的发展。同样,饲喂高脂(红花油)饮食的小鼠会出现血糖控制缺陷,高血糖症和肥胖症。为了评估适度增加GLUT4(胰岛素反应性葡萄糖转运蛋白)的表达对由脂肪喂养引起的血糖控制受损的影响,我们向高脂肪饮食喂养了携带GLUT4小基因的转基因小鼠。 GLUT4微型基因在转基因小鼠中的低水平组织特异性(心脏,骨骼肌和脂肪组织)表达阻止了脂肪喂养引起的血糖控制受损和伴随的高血糖症,但并未阻止肥胖。因此,GLUT4组织水平的小幅增加(<或= 2倍)可预防小鼠模型中糖尿病状态的主要症状,提示可能介入NIDDM的治疗。

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