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极低热量饮食逆转 2 型糖尿病大鼠模型高血糖的机制。

Mechanisms by which a Very-Low-Calorie Diet Reverses Hyperglycemia in a Rat Model of Type 2 Diabetes.

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA.

Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520, USA; Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing 100029, China.

出版信息

Cell Metab. 2018 Jan 9;27(1):210-217.e3. doi: 10.1016/j.cmet.2017.10.004. Epub 2017 Nov 9.

Abstract

Caloric restriction rapidly reverses type 2 diabetes (T2D), but the mechanism(s) of this reversal are poorly understood. Here we show that 3 days of a very-low-calorie diet (VLCD, one-quarter their typical intake) lowered plasma glucose and insulin concentrations in a rat model of T2D without altering body weight. The lower plasma glucose was associated with a 30% reduction in hepatic glucose production resulting from suppression of both gluconeogenesis from pyruvate carboxylase (V), explained by a reduction in hepatic acetyl-CoA content, and net hepatic glycogenolysis. In addition, VLCD resulted in reductions in hepatic triglyceride and diacylglycerol content and PKCɛ translocation, associated with improved hepatic insulin sensitivity. Taken together, these data show that there are pleotropic mechanisms by which VLCD reverses hyperglycemia in a rat model of T2D, including reduced DAG-PKCɛ-induced hepatic insulin resistance, reduced hepatic glycogenolysis, and reduced hepatic acetyl-CoA content, PC flux, and gluconeogenesis.

摘要

热量限制能迅速逆转 2 型糖尿病(T2D),但这种逆转的机制尚不清楚。在这里,我们发现在 T2D 大鼠模型中,连续 3 天的极低热量饮食(VLCD,仅为其典型摄入量的四分之一)可降低血浆葡萄糖和胰岛素浓度,而体重不变。较低的血浆葡萄糖与肝葡萄糖生成减少 30%有关,这是由于丙酮酸羧化酶(V)的糖异生受到抑制,肝乙酰辅酶 A 含量减少以及净肝糖原分解所致。此外,VLCD 还导致肝甘油三酯和二酰基甘油含量以及 PKCɛ易位减少,与改善肝胰岛素敏感性有关。综上所述,这些数据表明,VLCD 通过多种机制逆转 T2D 大鼠模型的高血糖,包括减少 DAG-PKCɛ 诱导的肝胰岛素抵抗,减少肝糖原分解以及减少肝乙酰辅酶 A 含量,PC 通量和糖异生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b20/5762419/ba6fe5901982/nihms914866f1.jpg

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