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Pomegranate extract prevents skeletal muscle of mice against wasting induced by acute TNF‐α injection
Author(s) -
Rodriguez Julie,
Caille Olivier,
Ferreira Daneel,
Francaux Marc
Publication year - 2017
Publication title -
molecular nutrition and food research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.495
H-Index - 131
eISSN - 1613-4133
pISSN - 1613-4125
DOI - 10.1002/mnfr.201600169
Subject(s) - skeletal muscle , inflammation , tumor necrosis factor alpha , pharmacology , c2c12 , chemistry , wasting , endocrinology , medicine , myogenesis
Scope We investigated whether punicalagin‐rich pomegranate extract (PE) protects skeletal muscle of mice against inflammation induced by an acute injection of TNF‐α. Results Mice fed with PE or standard chow during 6 wk were injected with TNF‐α (100 ng/g) or vehicle and sacrificed 6 h later. Prior supplementation with PE prevented the loss of tibialis anterior mass induced by TNF‐α. In skeletal muscle, the activation of the NF‐κB signaling and the induction of cytokines mRNA were reduced in mice having received PE. In those mice, the activity of the Akt/mTORC1 pathway and the protein synthesis were maintained after TNF‐α injection whereas markers involved in the ubiquitin proteasome pathway were less activated. As urolithin A was the only punicalagin metabolite detectable in plasma of mice supplemented with PE, we performed in vitro experiments using a murine cell line (C2C12) to provide evidence that urolithin A is likely the active compound protecting skeletal muscle against TNF‐α‐induced inflammation. Conclusion (focus on nutritional relevance) These results suggest that supplementation with a punicalagin‐rich PE may protect skeletal muscle against an acute inflammation.