J
Jonathan S. T. Woodhead
Researcher at University of Auckland
Publications - 21
Citations - 457
Jonathan S. T. Woodhead is an academic researcher from University of Auckland. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 7, co-authored 13 publications receiving 150 citations.
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Journal ArticleDOI
Circulatory exosomal miRNA following intense exercise is unrelated to muscle and plasma miRNA abundances.
Randall F. D'Souza,Jonathan S. T. Woodhead,Nina Zeng,Cherie Blenkiron,Troy L. Merry,David Cameron-Smith,David Cameron-Smith,Cameron J. Mitchell +7 more
TL;DR: The uniqueness of the exosomal miRNA response suggests its relevance as a sample pool that needs to be further explored in better understanding biological functions.
Journal ArticleDOI
MOTS-c is an exercise-induced mitochondrial-encoded regulator of age-dependent physical decline and muscle homeostasis
Joseph C. Reynolds,Rochelle W. Lai,Jonathan S. T. Woodhead,James H. Joly,Cameron J. Mitchell,Cameron J. Mitchell,David Cameron-Smith,Ryan Lu,Pinchas Cohen,Nicholas A. Graham,Bérénice A. Benayoun,Troy L. Merry,Troy L. Merry,Changhan Lee,Changhan Lee +14 more
TL;DR: In this paper, the authors showed that mitochondrial-encoded MOTS-c can significantly enhance physical performance in young (2 mo), middle-age (12 mo), and old (22 mo) mice.
Journal ArticleDOI
Mitochondrial-derived peptides in energy metabolism.
Troy L. Merry,Alex Chan,Jonathan S. T. Woodhead,Joseph C. Reynolds,Hiroshi Kumagai,Hiroshi Kumagai,Hiroshi Kumagai,Su-Jeong Kim,Changhan Lee,Changhan Lee +9 more
TL;DR: The evidence that endogenous MDPs are sensitive to changes in metabolism is reviewed, showing that metabolic conditions like obesity, diabetes and aging are associated with lower circulating MSPs and treatment of rodents with humanin, MOTS-c and SHLP2 can enhance insulin sensitivity and offer protection against a range of age-associated metabolic disorders.
Posted ContentDOI
MOTS-c is an Exercise-Induced Mitochondrial-Encoded Regulator of Age-Dependent Physical Decline and Muscle Homeostasis
Joseph C. Reynolds,Rochelle W. Lai,Jonathan S. T. Woodhead,James H. Joly,Cameron J. Mitchell,Cameron J. Mitchell,David Cameron-Smith,Ryan Lu,Pinchas Cohen,Nicholas A. Graham,Bérénice A. Benayoun,Troy L. Merry,Changhan Lee,Changhan Lee +13 more
TL;DR: MOTS-c is an exercise-induced mitochondrial-encoded peptide that significantly enhanced physical performance when administered to young, middle- aged, and old mice, indicating that aging is regulated by genes that are encoded not only in the nuclear genome, but also in the mitochondrial genome.
Journal ArticleDOI
Peripheral blood mononuclear cells do not reflect skeletal muscle mitochondrial function or adaptation to high-intensity interval training in healthy young men.
Christopher P. Hedges,Jonathan S. T. Woodhead,H. W. Wang,Cameron J. Mitchell,David Cameron-Smith,Anthony J. R. Hickey,Troy L. Merry +6 more
TL;DR: It is shown that in healthy young men, peripheral blood mononuclear cells do not reflect skeletal muscle mitochondrial function and do not adapt in response to a training intervention that increases Muscle mitochondrial function, suggesting PBMCs are a poor marker of muscle mitochondrialfunction in humans.