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哺乳期解偶联蛋白表达的抑制:瘦素的作用

Inhibition of uncoupling protein expression during lactation: role of leptin.

作者信息

Xiao Xiao Qiu, Grove Kevin L, Grayson Bernadette E, Smith M Susan

机构信息

Division of Neuroscience, Oregon National Primate Research Center, Oregon Health and Science University, 505 NW 185th Avenue, Beaverton, OR 97006, USA.

出版信息

Endocrinology. 2004 Feb;145(2):830-8. doi: 10.1210/en.2003-0836. Epub 2003 Nov 6.

Abstract

Uncoupling proteins (UCPs) are mitochondrial proteins that play a role in regulation of energy expenditure by uncoupling respiration from ATP synthesis. Lactation is a physiological condition characterized by negative energy balance due to the loss of energy sources to the production of milk. The objective of the current study was to investigate whether UCP mRNA and protein expressions were altered during lactation compared with those after 48 h of fasting. Lactation significantly reduced serum leptin levels, and removal of pups for 48 h increased serum leptin to higher levels than those observed in control rats. Compared with control rats, mRNA expression of UCP1 and UCP3 in brown adipose tissue (BAT) was dramatically reduced during lactation and fasting. The reduction in mRNAs was reflected by a lowered UCP1 protein level, and to some extent, UCP3 protein. Treatment of lactating rats with exogenous leptin (3 mg/kg) or removal of pups for 48 h completely reversed the down-regulation of UCP1 and UCP3 mRNA expression in BAT, and pup removal led to a recovery of protein expression. In contrast to BAT, UCP3 expression in skeletal muscle was increased in fasted rats and decreased during lactation. Similar changes were observed in serum free fatty acid levels. These changes are consistent with the idea that the utilization of free fatty acids as a fuel source is spared during lactation. As in BAT, leptin treatment and removal of pups were able to restore changes in mRNA expression of UCP3 in skeletal muscle during lactation. The present results suggest that the inhibition of leptin secretion during lactation is involved in the down-regulation of UCP expression in BAT and skeletal muscle, which, in turn, is responsible for the decrease in metabolic fuel oxidation and thermogenesis.

摘要

解偶联蛋白(UCPs)是线粒体蛋白,通过使呼吸与ATP合成解偶联,在能量消耗调节中发挥作用。哺乳是一种生理状态,其特征是由于能量用于产奶而导致能量负平衡。本研究的目的是调查与禁食48小时后相比,哺乳期间UCP mRNA和蛋白表达是否发生改变。哺乳显著降低血清瘦素水平,而将幼崽移除48小时会使血清瘦素水平升高至高于对照大鼠的水平。与对照大鼠相比,棕色脂肪组织(BAT)中UCP1和UCP3的mRNA表达在哺乳和禁食期间显著降低。mRNA的减少反映在UCP1蛋白水平降低,在一定程度上也反映在UCP3蛋白水平降低。用外源性瘦素(3 mg/kg)处理哺乳大鼠或移除幼崽48小时可完全逆转BAT中UCP1和UCP3 mRNA表达的下调,移除幼崽导致蛋白表达恢复。与BAT相反,禁食大鼠骨骼肌中UCP3表达增加,而在哺乳期间降低。血清游离脂肪酸水平也观察到类似变化。这些变化与以下观点一致,即哺乳期间游离脂肪酸作为燃料来源的利用被节省下来。与BAT一样,瘦素处理和移除幼崽能够恢复哺乳期间骨骼肌中UCP3 mRNA表达的变化。目前的结果表明,哺乳期间瘦素分泌的抑制参与了BAT和骨骼肌中UCP表达的下调,这反过来又导致代谢燃料氧化和产热减少。

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