Peroxiredoxin2 Deficiency Aggravates Aging-Induced Insulin Resistance and Declines Muscle Strength.


Journal

The journals of gerontology. Series A, Biological sciences and medical sciences
ISSN: 1758-535X
Titre abrégé: J Gerontol A Biol Sci Med Sci
Pays: United States
ID NLM: 9502837

Informations de publication

Date de publication:
16 01 2019
Historique:
received: 31 10 2017
accepted: 03 05 2018
pubmed: 8 5 2018
medline: 2 11 2019
entrez: 8 5 2018
Statut: ppublish

Résumé

This study examined the role of peroxiredoxin2 (Prx2) in aging-induced insulin resistance and reduction in skeletal muscle function in young (2-month-old) and old (24-month-old) Prx2 knockout (KO) and wild-type mice. Plasma insulin levels increased with aging in Prx2 KO mice but not in wild-type mice. Insulin sensitivity in the whole-body and skeletal muscle as assessed with the hyperinsulinemic-euglycemic clamp was lower in Prx2 KO mice than in wild-type mice in the old group but was not significantly different between the two genotypes in the young group. Insulin-induced activation of intracellular signaling molecules was also suppressed in old Prx2 KO mice compared to their wild-type littermates. Oxidative stress, inflammation, and p53 expression levels in skeletal muscle were higher in Prx2 KO mice than in wild-type mice in the old group but were not different between the two genotypes in the young group. p53 expression was negatively correlated with skeletal muscle insulin sensitivity in old mice. Skeletal muscle mass was similar between the two genotypes but grip strength was reduced in old Prx2 KO mice compared to old wild-type mice. These results suggest that Prx2 plays a protective role in aging-induced insulin resistance and declines in muscle strength by suppressing oxidative stress.

Identifiants

pubmed: 29733327
pii: 4992680
doi: 10.1093/gerona/gly113
doi:

Substances chimiques

Homeodomain Proteins 0
Insulin 0
Prrx2 protein, mouse 0
RNA 63231-63-0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

147-154

Auteurs

Hye-Na Cha (HN)

Department of Physiology, College of Medicine, Yeungnam University, Daegu, Korea.
Smart-Aging Convergence Research Center, College of Medicine, Yeungnam University, Daegu, Korea.

Soyoung Park (S)

Department of Physiology, College of Medicine, Yeungnam University, Daegu, Korea.
Smart-Aging Convergence Research Center, College of Medicine, Yeungnam University, Daegu, Korea.

Yongwook Dan (Y)

Weinberg College of Art and Sciences, Northwestern University, Chicago, Illinois.

Jae-Ryong Kim (JR)

Smart-Aging Convergence Research Center, College of Medicine, Yeungnam University, Daegu, Korea.
Department of Biochemistry and Molecular Biology, College of Medicine, Yeungnam University, Daegu, Korea.

So-Young Park (SY)

Department of Physiology, College of Medicine, Yeungnam University, Daegu, Korea.
Smart-Aging Convergence Research Center, College of Medicine, Yeungnam University, Daegu, Korea.

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Classifications MeSH