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Journal of animal science2009; 87(8); 2528-2535; doi: 10.2527/jas.2009-1845

Developmental changes in the concentrations of glutamine and other amino acids in plasma and skeletal muscle of the Standardbred foal.

Abstract: Glutamine is concentrated within skeletal muscle, where it has been proposed to play a regulatory role in maintaining protein homeostasis. The work presented here addressed the hypothesis that glutamine would be the most abundant free alpha-AA in plasma and skeletal muscle in the foal during the first year of life. Glycine, however, was the most abundant free alpha-AA in plasma at birth and between 3 and 12 mo of age. The concentration of glutamine, the second most abundant AA at birth, increased through the first 7 d (P < 0.05) and then returned to values similar to those at birth. This resulted in glutamine being the most abundant free alpha-AA in plasma from 1 d through 1 mo of age. The most abundant free alpha-AA in skeletal muscle at birth was glutamine, but the concentration fell by more than 50% by d 15 and continued to decrease, reaching about one-third of the original values by 1 yr of age (P < 0.05). Glutamine synthetase was barely detectable in skeletal muscle at birth, but the abundance increased rapidly within 15 d of birth. The concentration of glycine, the second most abundant alpha AA in muscle at birth, decreased by about 40% by d 15 (P < 0.05) and then stabilized at this value throughout the year. In contrast, glutamate, alanine, and serine concentrations, the third, fourth, and fifth most abundant free alpha-AA in muscle at birth, respectively, increased to new stable concentrations between 3 and 6 mo of age (P < 0.05). This resulted in alanine being the most abundant free alpha-AA in skeletal muscle at 12 mo of age, followed by glutamate, glutamine, and glycine. The decrease in intramuscular glutamine content, particularly during the first 2 wk after birth, is not compatible with a regulatory role for glutamine in muscle protein synthesis because it occurred at the time of maximum growth in these animals. The findings that, at certain times of development, glutamine was not the most abundant free alpha-AA in the foal is novel and signifies that intramuscular glutamine may have functions specific to muscle type and mammalian species.
Publication Date: 2009-04-24 PubMed ID: 19395517DOI: 10.2527/jas.2009-1845Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research study focuses on the changes in the concentration of the amino acid glutamine in the plasma and skeletal muscle of Standardbred foals during their first year of life. It was observed that while the concentration of glutamine was initially the highest, other amino acids like glycine and alanine became more abundant over time.

Study Focus

  • The study primarily aimed at testing the hypothesis that glutamine would be the most concentrated alpha-amino acid (alpha-AA) in the plasma and skeletal muscle of foals during their first year.
  • It also investigated the regulatory role of glutamine in maintaining protein balance in the skeletal muscle.

Key Observations and Findings

  • Contrary to the initial hypothesis, glycine was found to be the most abundant alpha-AA in the plasma at birth and between 3 to 12 months of age.
  • Glutamine, while being the second most abundant AA at birth, increased during the first 7 days and became the most abundant alpha-AA in plasma from 1 day to 1 month of age.
  • In the skeletal muscle, glutamine’s concentration which was the highest at birth, fell by more than half by day 15 and reduced to about one-third of the original values by the end of the year.
  • Glutamine synthetase, which is vital for the synthesis of glutamine, was barely detectable in the skeletal muscle at birth but saw a rapid increase within 15 days of birth.
  • By the end of 12 months, alanine turned out to be the most abundant alpha-AA in the skeletal muscle, followed by glutamate, glutamine, and glycine.

Conclusions and Implications

  • The findings contradict the proposed regulatory role of glutamine in muscle protein synthesis, given the decrease in its concentration when the maximum growth was observed.
  • The results indicated that, at certain stages of development, glutamine was not the most abundant alpha-AA, suggesting it may have specific functions depending on the muscle type and species.
  • The study emphasizes a possible significant role of other amino acids like glycine and alanine in the foal’s development and growth, warranting further investigation.

Cite This Article

APA
Manso Filho HC, McKeever KH, Gordon ME, Manso HE, Lagakos WS, Wu G, Watford M. (2009). Developmental changes in the concentrations of glutamine and other amino acids in plasma and skeletal muscle of the Standardbred foal. J Anim Sci, 87(8), 2528-2535. https://doi.org/10.2527/jas.2009-1845

Publication

ISSN: 1525-3163
NlmUniqueID: 8003002
Country: United States
Language: English
Volume: 87
Issue: 8
Pages: 2528-2535

Researcher Affiliations

Manso Filho, H C
  • Department of Animal Sciences, Rutgers the State University of New Jersey, New Brunswick, NJ 08901, USA.
McKeever, K H
    Gordon, M E
      Manso, H E
        Lagakos, W S
          Wu, G
            Watford, M

              MeSH Terms

              • Animals
              • Body Composition
              • Female
              • Gene Expression Regulation, Developmental / physiology
              • Gene Expression Regulation, Enzymologic / physiology
              • Glutamate-Ammonia Ligase / metabolism
              • Glutamine / blood
              • Horses / growth & development
              • Horses / metabolism
              • Male
              • Muscle, Skeletal / metabolism

              Citations

              This article has been cited 1 times.
              1. Knight LS, Piibe Q, Lambie I, Perkins C, Yancey PH. Betaine in the Brain: Characterization of Betaine Uptake, its Influence on Other Osmolytes and its Potential Role in Neuroprotection from Osmotic Stress. Neurochem Res 2017 Dec;42(12):3490-3503.
                doi: 10.1007/s11064-017-2397-3pubmed: 28918494google scholar: lookup