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      Nutrient regulation of somatic growth in teleost fish. The interaction between somatic growth, feeding and metabolism

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      Molecular and Cellular Endocrinology
      Elsevier BV

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          mTOR signaling in growth control and disease.

          The mechanistic target of rapamycin (mTOR) signaling pathway senses and integrates a variety of environmental cues to regulate organismal growth and homeostasis. The pathway regulates many major cellular processes and is implicated in an increasing number of pathological conditions, including cancer, obesity, type 2 diabetes, and neurodegeneration. Here, we review recent advances in our understanding of the mTOR pathway and its role in health, disease, and aging. We further discuss pharmacological approaches to treat human pathologies linked to mTOR deregulation. Copyright © 2012 Elsevier Inc. All rights reserved.
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            A PGC1α-dependent myokine that drives browning of white fat and thermogenesis

            Exercise benefits a variety of organ systems in mammals, and some of the best-recognized effects of exercise on muscle are mediated by the transcriptional coactivator PGC1α Here we show that PGC1α expression in muscle stimulates an increase in expression of Fndc5, a membrane protein that is cleaved and secreted as a new hormone, irisin. Irisin acts on white adipose cells in culture and in vivo to stimulate UCP1 expression and a broad program of brown fat-like development. Irisin is induced with exercise in mice and humans, and mildly increased irisin levels in blood cause an increase in energy expenditure in mice with no changes in movement or food intake. This results in improvements in obesity and glucose homeostasis. Irisin could be a protein therapeutic for human metabolic disease and other disorders that are improved with exercise.
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              Positional cloning of the mouse obese gene and its human homologue.

              The mechanisms that balance food intake and energy expenditure determine who will be obese and who will be lean. One of the molecules that regulates energy balance in the mouse is the obese (ob) gene. Mutation of ob results in profound obesity and type II diabetes as part of a syndrome that resembles morbid obesity in humans. The ob gene product may function as part of a signalling pathway from adipose tissue that acts to regulate the size of the body fat depot.
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                Author and article information

                Journal
                Molecular and Cellular Endocrinology
                Molecular and Cellular Endocrinology
                Elsevier BV
                03037207
                December 2020
                December 2020
                : 518
                : 111029
                Article
                10.1016/j.mce.2020.111029
                32941926
                90ee4675-7dbc-4dae-b684-1144aaa09920
                © 2020

                https://www.elsevier.com/tdm/userlicense/1.0/

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