Arginine and proline metabolism is associated with older adult skeletal muscle mass and altered by inflammation in primary human muscle cells
Loading...
No Access Until
Permanent Link(s)
Collections
Other Titles
Authors
Abstract
Age-related loss of skeletal muscle mass (sarcopenia) adversely affects muscle tissue-specific and whole-body homeostasis, suggesting an undefined relationship between muscle mass and whole-body circulation that underlies the etiology of sarcopenia.
To investigate, 344 metabolites and analytes were measured in serum from 19 older adults. Arginine and proline metabolism was the pathway most closely associated with skeletal muscle index (SMI), a measure of skeletal muscle mass. Subsequently, gene expression of related transport and regulatory enzymes was measured.
Younger and older adult muscle tissue had similar inflammatory signaling and gene expression of CAT-1 and CAT-2, the cationic amino acid transporters that allow arginine into muscle. However, the proinflammatory cytokine TNF-α increased CAT-2 gene expression in differentiated human primary skeletal muscle cells. TNF-α also altered the expression of arginine metabolic genes regulating polyamine synthesis and proline production.
Changes in arginine availability and metabolism may underlie the relationship between inflammation and skeletal muscle mass.
Journal / Series
Volume & Issue
Description
Sponsorship
Date Issued
2017-08-30
Publisher
Keywords
Nutrition; metabolomics; arginine metabolism; inflammation susceptibility; myoblasts; sarcopenia
Location
Effective Date
Expiration Date
Sector
Employer
Union
Union Local
NAICS
Number of Workers
Committee Chair
Thalacker-Mercer, Anna E.
Committee Co-Chair
Committee Member
Libert, Sergiy
Brenna, James Thomas
Gu, Zhenglong
Brenna, James Thomas
Gu, Zhenglong
Degree Discipline
Nutrition
Degree Name
M.S., Nutrition
Degree Level
Master of Science
Related Version
Related DOI
Related To
Related Part
Based on Related Item
Has Other Format(s)
Part of Related Item
Related To
Related Publication(s)
Link(s) to Related Publication(s)
References
Link(s) to Reference(s)
Previously Published As
Government Document
ISBN
ISMN
ISSN
Other Identifiers
Rights
Rights URI
Types
dissertation or thesis