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氨基酸和胰岛素是新生仔猪肌肉蛋白质合成的调节因子。

Amino acids and insulin are regulators of muscle protein synthesis in neonatal pigs.

作者信息

Davis T A, Suryawan A, Orellana R A, Fiorotto M L, Burrin D G

机构信息

United States Department of Agriculture/Agriculture Research Service Children's Nutrition Research Center, Baylor College of Medicine, Houston, TX 77030, USA.

出版信息

Animal. 2010;4(11):1790-1796. doi: 10.1017/S1751731110000984.

Abstract

The stage of development between birth and weaning in mammals is a period of very rapid growth that is crucial for the long-term well-being of the animal. The rate of protein deposition in neonatal animals is very high because dietary protein is efficiently utilized to increase body protein mass. Our studies in neonatal pigs have shown that this high efficiency of protein deposition is largely due to the marked increase in protein synthesis after feeding, and this response is particularly profound in the skeletal muscle. The enhanced stimulation of muscle protein synthesis in neonates after feeding is independently mediated by the rise in insulin and amino acids and this response declines with age. Intracellular signaling components that respond to the postprandial rise in amino acids and insulin have been identified and their activation has been shown to be elevated in skeletal muscle of neonatal pigs after a meal and to decrease with development. The enhanced activation of these components in the amino acid and insulin signaling pathways in neonatal muscle contributes to the high rate of muscle protein synthesis and rapid gain in skeletal muscle mass in newborn pigs, which are essential determinants of efficient growth during development.

摘要

哺乳动物从出生到断奶的发育阶段是一个生长非常迅速的时期,对动物的长期健康至关重要。新生动物的蛋白质沉积率非常高,因为膳食蛋白质被有效地用于增加身体蛋白质质量。我们对新生仔猪的研究表明,这种高蛋白沉积效率很大程度上归因于进食后蛋白质合成的显著增加,并且这种反应在骨骼肌中尤为明显。新生动物进食后肌肉蛋白质合成的增强刺激是由胰岛素和氨基酸的升高独立介导的,并且这种反应会随着年龄的增长而下降。已经确定了对餐后氨基酸和胰岛素升高作出反应的细胞内信号成分,并且它们的激活在新生仔猪进食后的骨骼肌中升高,并随着发育而降低。新生肌肉中氨基酸和胰岛素信号通路中这些成分的增强激活有助于新生仔猪肌肉蛋白质的高合成率和肌肉质量的快速增加,而这是发育过程中高效生长的重要决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df27/3139366/c7dfbecbd1a0/nihms306146f1.jpg

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