AI Article Synopsis

  • Obestatin/GPR39 signaling is crucial in promoting skeletal muscle growth and repair through both G-protein-dependent and -independent pathways, involving various proteins.
  • This signaling helps determine the oxidative fiber type in muscles, impacting their formation and metabolic properties.
  • Increased activity of Mef2 and PGC-1α from obestatin signaling enhances muscle oxidative capacity and myofiber growth, indicating its role in muscle fiber-type programming.

Article Abstract

Obestatin/GPR39 signaling stimulates skeletal muscle growth and repair by inducing both G-protein-dependent and -independent mechanisms linking the activated GPR39 receptor with distinct sets of accessory and effector proteins. In this work, we describe a new level of activity where obestatin signaling plays a role in the formation, contractile properties and metabolic profile of skeletal muscle through determination of oxidative fiber type. Our data indicate that obestatin regulates Mef2 activity and PGC-1α expression. Both mechanisms result in a shift in muscle metabolism and function. The increase in Mef2 and PGC-1α signaling activates oxidative capacity, whereas Akt/mTOR signaling positively regulates myofiber growth. Taken together, these data indicate that the obestatin signaling acts on muscle fiber-type program in skeletal muscle.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5437042PMC
http://dx.doi.org/10.1038/s41598-017-02337-4DOI Listing

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