The Protein and Energy Metabolic Response of Skeletal Muscle to the Low-Protein Diets in Growing Pigs

J Agric Food Chem. 2017 Oct 4;65(39):8544-8551. doi: 10.1021/acs.jafc.7b02461. Epub 2017 Sep 26.

Abstract

This study was conducted to determine the effect of low-protein diets on protein and energy metabolism in skeletal muscle, and to elucidate the underlying mechanism. A total of 18 growing pigs (average initial body weight = 36.47 kg) were individually penned and assigned to three treatments; each treatment was fed one of three diets containing either 18%, 15%, or 12% CP. The results showed that reducing dietary CP contents decreased (P < 0.05) the weight of half Longissimus dorsi (LD) muscle and serum concentration of insulin-like growth factor 1 (IGF-1). Compared with the 18% and 15% CP treatments, the 12% CP treatment suppressed (P < 0.05) the components of mammalian target of rapamycin complex 1 (mTORC1) pathway, but upregulated (P < 0.05) the mRNA levels for proteolysis-related genes, and concomitantly caused an increase (P < 0.05) in the percentage of apoptotic cells in LD muscle. Along with lower (P < 0.05) AMP/ATP ratio and greater (P < 0.05) energy charge value in LD muscle of the 12% CP treatment, there was a concurrent decrease (P < 0.05) in the proteins for AMP-activated protein kinase α (AMPKα) pathway. Likewise, these results were also observed in the Biceps femoris muscle with slightly different degree of impacts. These results indicate that the retardation effect of low-protein supply on muscle growth of growing pigs could be likely regulated by inhibiting IGF-1/mTORC1 protein synthesis cascade, along with strong alterations in energy status and AMPKα pathway.

Keywords: energy status; low-protein diet; muscle; pig; protein metabolism.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Animal Nutritional Physiological Phenomena
  • Animals
  • Apoptosis
  • Diet, Protein-Restricted / veterinary*
  • Dietary Proteins / administration & dosage
  • Energy Metabolism*
  • Insulin-Like Growth Factor I / analysis
  • Mechanistic Target of Rapamycin Complex 1 / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Muscle, Skeletal / metabolism*
  • Proteolysis
  • RNA, Messenger / analysis
  • Sus scrofa / growth & development*
  • Sus scrofa / metabolism*
  • Transcriptome

Substances

  • Dietary Proteins
  • Muscle Proteins
  • RNA, Messenger
  • Insulin-Like Growth Factor I
  • Mechanistic Target of Rapamycin Complex 1
  • AMP-Activated Protein Kinases