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饮食诱导的肥胖改变蛋白质合成:禁食与进食小鼠的组织特异性影响。

Diet-induced obesity alters protein synthesis: tissue-specific effects in fasted versus fed mice.

作者信息

Anderson Stephanie R, Gilge Danielle A, Steiber Alison L, Previs Stephen F

机构信息

Department of Nutrition, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA.

出版信息

Metabolism. 2008 Mar;57(3):347-54. doi: 10.1016/j.metabol.2007.10.009.

Abstract

The influence of obesity on protein dynamics is not clearly understood. We have designed experiments to test the hypothesis that obesity impairs the stimulation of tissue-specific protein synthesis after nutrient ingestion. C57BL/6J mice were randomized into 2 groups: group 1 (control, n = 16) was fed a low-fat, high-carbohydrate diet, whereas group 2 (experimental, n = 16) was fed a high-fat, low-carbohydrate diet ad libitum for 9 weeks. On the experiment day, all mice were fasted for 6 hours and given an intraperitoneal injection of (2)H(2)O. They were then randomized into 2 subgroups and either given a sham saline gavage or a liquid-meal challenge. Rates of protein synthesis were determined via the incorporation of [(2)H]alanine (5 hours postchallenge) into total gastrocnemius muscle protein, total liver protein, and plasma albumin. High-fat feeding led to an increase in total body fat (P < .001) and epididymal fat pad weights (P < .001) and elevated fasting plasma glucose levels (P < .01). Diet-induced obesity (a) did not affect basal rates of skeletal muscle protein synthesis, but did impair the activation of skeletal muscle protein synthesis in response to nutrient ingestion (P < .05), and (b) slightly reduced basal rates of synthesis of total hepatic proteins and plasma albumin (P = .10), but did not affect the synthesis of either in response to the meal challenge. In conclusion, there are alterations in tissue-specific protein metabolism in the C57BL/6J mouse model of diet-induced obesity. This model may prove to be helpful in future studies that explore the mechanisms that account for altered protein dynamics in obesity.

摘要

肥胖对蛋白质动力学的影响尚不清楚。我们设计了实验来检验这一假设,即肥胖会损害营养摄入后组织特异性蛋白质合成的刺激作用。将C57BL/6J小鼠随机分为2组:第1组(对照组,n = 16)喂食低脂、高碳水化合物饮食,而第2组(实验组,n = 16)随意喂食高脂、低碳水化合物饮食9周。在实验当天,所有小鼠禁食6小时,然后腹腔注射(2)H(2)O。然后将它们随机分为2个亚组,分别给予假盐水灌胃或液体餐刺激。通过将[(2)H]丙氨酸(刺激后5小时)掺入腓肠肌总蛋白、肝脏总蛋白和血浆白蛋白中来测定蛋白质合成速率。高脂喂养导致全身脂肪增加(P <.001)和附睾脂肪垫重量增加(P <.001),并使空腹血糖水平升高(P <.01)。饮食诱导的肥胖(a)不影响骨骼肌蛋白质合成的基础速率,但确实损害了营养摄入后骨骼肌蛋白质合成的激活(P <.05),并且(b)略微降低了肝脏总蛋白和血浆白蛋白合成的基础速率(P =.10),但不影响餐食刺激后两者的合成。总之,在饮食诱导肥胖的C57BL/6J小鼠模型中,组织特异性蛋白质代谢存在改变。该模型可能有助于未来探索肥胖中蛋白质动力学改变机制的研究。

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