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We hypothesized that the muscle protein anabolic resistance to amino acids occurs in older adults and that RET could overcome such anabolic resistance by enhancing mTORC1 signaling and MPSactivity." "We found that RET enhanced MPS during muscle protein anabolism in aging and that this may explain some of the aging-related decline in muscle mass," said Dr. Zavala. "Furthermore, we found that RET increases the synthesis of the protein substrates the primary target of the anabolic and catabolic mechanisms of muscle protein anabolic resistance." The researchers found that anabolic resistance could improve muscle mass by stimulating mTORC1 (muscle spiking) and mAMPK (anabolic phosphatase kinase) activity, which stimulates mTORC1 signaling to induce mTORC1-driven phosphorylation of p70S6K-AKT and p45S6K-AKT. Thus, they found that these protein substrates are crucial for skeletal muscle anabolism. "This is the first evidence that the effects of RET on the anabolic resistance to amino acids also extend to the degradation of substrate protein substrates, which we have previously shown in older adults. These findings are relevant both for older adults' capacity to synthesize these substrates for cellular function and for elderly muscle aging," said Zavala. In turn, the researchers studied the effect of mTORC1-driven mAMPK signaling on RET at the mRNA level in rat skeletal muscle. They found that RET suppressed AMPK in muscle and at the mRNA level, which supports their hypothesis that mTORC1 increases activation of mAMPK and mAMPK stimulates RET. RET stimulates phosphorylation and cAMP production of p70S6K-AKT and p45S6K's and enhanced this phosphorylation by stimulating the expression of mTORC1; thus, RET could enhance muscle protein anabolic resistance to amino acids. In addition to increasing p70S6K-AKT as well as mAMPK, the authors found that RET suppressed p45S6K-AKT activity. Finally, mTORC1 could inhibit AMPK's effects by targeting phosphorylation, which limits the effects of RET on muscle protein anabolic resistance to amino acids. "An important observation of RET is its ability to enhance mTORC1 signaling so that protein substrates could be degraded as part of skeletal muscle maintenance." said Zavala. "An implication of this is that RET may enhance muscle protein anabolism in aging and possibly may provide a mechanism for enhancing muscle mass after sarcopenia and bone homeostasis declines, which are important Similar articles:
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