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Regulation of human metabolism by hypoxia-inducible factor

Research output: Contribution to journalArticlepeer-review

Federico Formenti, Dumitru Constantin-Teodosiu, Yaso Emmanuel, Jane Cheeseman, Keith L Dorrington, Lindsay Martin Edwards, Sandy M Humphreys, Terence R J Lappin, Mary-Frances McMullin, Christopher J. McNamara, Wendy Mills, John Murphy, David F O'Connor, Melanie J Percy, Peter J. Ratcliffe, Thomas G Smith, Marilyn Treacy, Keith N Frayn, Paul L Greenhaff, Fredrik Karpe & 2 more Kieran Clarke, Peter A. Robbins

Original languageEnglish
Pages (from-to)12722-12727
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Issue number28
Published13 Jul 2010


  • PNAS-2010-Formenti-12722-7

    PNAS_2010_Formenti_12722_7.pdf, 701 KB, application/pdf

    Uploaded date:30 Jun 2016

    Version:Final published version

King's Authors


The hypoxia-inducible factor (HIF) family of transcription factors directs a coordinated cellular response to hypoxia that includes the transcriptional regulation of a number of metabolic enzymes. Chuvash polycythemia (CP) is an autosomal recessive human disorder in which the regulatory degradation of HIF is impaired, resulting in elevated levels of HIF at normal oxygen tensions. Apart from the polycythemia, CP patients have marked abnormalities of cardiopulmonary function. No studies of integrated metabolic function have been reported. Here we describe the response of these patients to a series of metabolic stresses: exercise of a large muscle mass on a cycle ergometer, exercise of a small muscle mass (calf muscle) which allowed noninvasive in vivo assessments of muscle metabolism using (31)P magnetic resonance spectroscopy, and a standard meal tolerance test. During exercise, CP patients had early and marked phosphocreatine depletion and acidosis in skeletal muscle, greater accumulation of lactate in blood, and reduced maximum exercise capacities. Muscle biopsy specimens from CP patients showed elevated levels of transcript for pyruvate dehydrogenase kinase, phosphofructokinase, and muscle pyruvate kinase. In cell culture, a range of experimental manipulations have been used to study the effects of HIF on cellular metabolism. However, these approaches provide no potential to investigate integrated responses at the level of the whole organism. Although CP is relatively subtle disorder, our study now reveals a striking regulatory role for HIF on metabolism during exercise in humans. These findings have significant implications for the development of therapeutic approaches targeting the HIF pathway.

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