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  • 1.
    Olsson, M Charlotte
    et al.
    Uppsala University, Department of Neuroscience, Clinical Neurophysiology, Ing 85 3 tr., 751 85 Uppsala, Sweden.
    Krüger, Martina
    University of Münster, Physiology and Biophysics Unit, Schlossplatz 5, D-48149 Münster, Germany .
    Meyer, Lars-Henrik
    University of Münster, Physiology and Biophysics Unit, Schlossplatz 5, D-48149 Münster, Germany .
    Ahnlund, Lena
    Rehabilitation Medicine, 75185 Uppsala, Sweden.
    Gransberg, Lennart
    Uppsala University, Department of Neuroscience, Clinical Neurophysiology, Ing 85 3 tr., 751 85 Uppsala, Sweden.
    Linke, Wolfgang A
    University of Münster, Physiology and Biophysics Unit, Schlossplatz 5, D-48149 Münster, Germany.
    Larsson, Lars
    Uppsala University, Department of Neuroscience, Clinical Neurophysiology, Ing 85 3 tr., 751 85 Uppsala, Sweden.
    Fibre type-specific increase in passive muscle tension in spinal cord-injured subjects with spasticity2006In: Journal of Physiology, ISSN 0022-3751, E-ISSN 1469-7793, Vol. 577, no 1, p. 339-352Article in journal (Refereed)
  • 2.
    Russell, Aaron P.
    et al.
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Lamon, Severine
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Boon, Hanneke
    Department of Molecular Medicine and Surgery, Integrative Physiology, Karolinska Institutet, Stockholm, Sweden.
    Wada, Shogo
    Division of Regenerative Medical Engineering, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
    Güller, Isabelle
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Brown, Erin L.
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Chibalin, Alexander V.
    Department of Molecular Medicine and Surgery, Integrative Physiology, Karolinska Institutet, Stockholm, Sweden.
    Zierath, Juleen R.
    Department of Molecular Medicine and Surgery, Integrative Physiology, Karolinska Institutet, Stockholm, Sweden.
    Snow, Rod J.
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Stepto, Nigel
    School of Sports and Exercise Science, Victoria University, Footscray, Australia.
    Wadley, Glenn D.
    Centre for Physical Activity and Nutrition Research, School of Exercise and Nutrition Sciences, Deakin University, Burwood, Australia.
    Akimoto, Takayuki
    Division of Regenerative Medical Engineering, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
    Regulation of miRNAs in human skeletal muscle following acute endurance exercise and short-term endurance training2013In: Journal of Physiology, ISSN 0022-3751, E-ISSN 1469-7793, Vol. 591, no 18, p. 4637-4653Article in journal (Refereed)
    Abstract [en]

    The identification of microRNAs (miRNAs) has established new mechanisms that control skeletal muscle adaptation to exercise. The present study investigated the mRNA regulation of components of the miRNA biogenesis pathway (Drosha, Dicer and Exportin-5), muscle enriched miRNAs, (miR-1, -133a, -133b and -206), and several miRNAs dysregulated in muscle myopathies (miR-9, -23, -29, -31 and -181). Measurements were made in muscle biopsies from nine healthy untrained males at rest, 3 h following an acute bout of moderate-intensity endurance cycling and following 10 days of endurance training. Bioinformatics analysis was used to predict potential miRNA targets. In the 3 h period following the acute exercise bout, Drosha, Dicer and Exportin-5, as well as miR-1, -133a, -133-b and -181a were all increased. In contrast miR-9, -23a, -23b and -31 were decreased. Short-term training increased miR-1 and -29b, while miR-31 remained decreased. Negative correlations were observed between miR-9 and HDAC4 protein (r=-0.71; P= 0.04), miR-31 and HDAC4 protein (r =-0.87; P= 0.026) and miR-31 and NRF1 protein (r =-0.77; P= 0.01) 3 h following exercise. miR-31 binding to the HDAC4 and NRF1 3′ untranslated region (UTR) reduced luciferase reporter activity. Exercise rapidly and transiently regulates several miRNA species in muscle. Several of these miRNAs may be involved in the regulation of skeletal muscle regeneration, gene transcription and mitochondrial biogenesis. Identifying endurance exercise-mediated stress signals regulating skeletal muscle miRNAs, as well as validating their targets and regulatory pathways post exercise, will advance our understanding of their potential role/s in human health. © 2013 The Authors. The Journal of Physiology © 2013 The Physiological Society.

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