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对肥胖的糖尿病前期大鼠进行热量限制可防止β细胞耗竭、β细胞葡萄糖转运蛋白2丢失以及葡萄糖代谢功能不全。

Caloric restriction in obese pre-diabetic rats prevents beta-cell depletion, loss of beta-cell GLUT 2 and glucose incompetence.

作者信息

Ohneda M, Inman L R, Unger R H

机构信息

Center for Diabetes Research, University of Texas Southwestern Medical Center, Dallas, USA.

出版信息

Diabetologia. 1995 Feb;38(2):173-9. doi: 10.1007/BF00400091.

DOI:10.1007/BF00400091
PMID:7713311
Abstract

Pre-diabetic male Zucker diabetic fatty rats (ZDF) become diabetic between 8 and 10 weeks of age. At that time their beta cells exhibit high basal insulin secretion, absent insulin response to glucose and loss of GLUT 2 glucose transporter. Beta-cell volume, which is increased at the onset of non-insulin-dependent diabetes, declines precipitously by age 18 weeks. To determine if expression of this diabetic phenotype was dependent upon the increased food intake of these rats, they were diet-matched to lean littermates for 12 weeks beginning at 6 weeks of age. Untreated control ZDF rats received an unrestricted diet for 3 months. All of the controls became hyperglycaemic by 8 weeks of age, whereas all diet-matched rats remained euglycaemic throughout the 3 months, despite the fact that at 18 weeks of age their mean body weight equaled that of obese rats on an unrestricted diet. In the former rats glucose-stimulated insulin secretion was absent at 12 weeks of age and GLUT-2-positive beta cells had fallen below 30%. The volume fraction of their beta cells was 2.6 times normal at this age but by 18 weeks of age it had declined by 75%. Diet restriction for 3 months prevented the loss of glucose-stimulated insulin secretion and the reduction of beta-cell GLUT-2 and beta-cell volume fraction. However, neither the elevated basal insulin secretion nor the exaggerated arginine-stimulated insulin secretion of the obese rats was reversed or prevented by caloric restriction.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

糖尿病前期雄性Zucker糖尿病脂肪大鼠(ZDF)在8至10周龄时会发展为糖尿病。此时,它们的β细胞表现出高基础胰岛素分泌、对葡萄糖无胰岛素反应以及GLUT 2葡萄糖转运体缺失。在非胰岛素依赖型糖尿病发病时增加的β细胞体积,到18周龄时急剧下降。为了确定这种糖尿病表型的表达是否依赖于这些大鼠增加的食物摄入量,从6周龄开始,将它们与瘦的同窝大鼠进行饮食匹配,为期12周。未治疗的对照ZDF大鼠接受无限制饮食3个月。所有对照组在8周龄时都出现了高血糖,而所有饮食匹配的大鼠在整个3个月中都保持血糖正常,尽管在18周龄时它们的平均体重与无限制饮食的肥胖大鼠相当。在前者中,12周龄时葡萄糖刺激的胰岛素分泌缺失,GLUT - 2阳性β细胞降至30%以下。此时它们的β细胞体积分数是正常的2.6倍,但到18周龄时下降了75%。3个月的饮食限制防止了葡萄糖刺激的胰岛素分泌的丧失以及β细胞GLUT - 2和β细胞体积分数的降低。然而,热量限制既没有逆转也没有防止肥胖大鼠基础胰岛素分泌升高或精氨酸刺激的胰岛素分泌过度。(摘要截断于250字)

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Immunoassay of endogenous plasma insulin in man.人体内源性血浆胰岛素的免疫测定。
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GLUT2 expression and function in beta-cells of GK rats with NIDDM. Dissociation between reductions in glucose transport and glucose-stimulated insulin secretion.非胰岛素依赖型糖尿病(NIDDM)GK大鼠β细胞中葡萄糖转运蛋白2(GLUT2)的表达与功能。葡萄糖转运减少与葡萄糖刺激的胰岛素分泌之间的分离。
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Impact of diet restriction in the management of diabetes: evidences from preclinical studies.饮食限制在糖尿病管理中的影响:来自临床前研究的证据。
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Long-term exposure of rat pancreatic islets to fatty acids inhibits glucose-induced insulin secretion and biosynthesis through a glucose fatty acid cycle.大鼠胰岛长期暴露于脂肪酸会通过葡萄糖脂肪酸循环抑制葡萄糖诱导的胰岛素分泌和生物合成。
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Beta-cell lipotoxicity in the pathogenesis of non-insulin-dependent diabetes mellitus of obese rats: impairment in adipocyte-beta-cell relationships.肥胖大鼠非胰岛素依赖型糖尿病发病机制中的β细胞脂毒性:脂肪细胞与β细胞关系受损。
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Coated charcoal immunoassay of insulin.胰岛素的包被炭免疫测定法。
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