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Peroxisome proliferator-activated receptor expression is reduced in skeletal muscle in COPD
Open accessAbstract
Chronic obstructive pulmonary disease (COPD) is a multiorgan systemic disease. The systemic features are skeletal muscle weakness and cachexia, the latter being associated with systemic inflammation. The exact mechanisms underlying skeletal muscle dysfunction in COPD remain obscure. Recent evidence suggests involvement of the peroxisome proliferator-activated receptors (PPARs) and PPAR-γ coactivator (PGC)-1α in regulation of skeletal muscle morphology and metabolism, and mitochondrial transcription factor A (TFAM) has been implicated in the process of mitochondrial biogenesis. The aim of the present exploratory study was, therefore, to compare these factors in the skeletal muscle of nine healthy control subjects and 14 COPD patients stratified by cachexia. PPAR-γ, PPAR-δ and TFAM were measured at the mRNA and protein level by real-time quantitative PCR and Western blotting, respectively. PPAR-α and PGC-1α were meansured at the mRNA level. PPAR-δ and TFAM protein content, as well as PGC-1α mRNA levels, were decreased in the skeletal muscle of COPD patients compared with healthy controls. The cachectic COPD subgroup was further characterised by decreased PPAR-α mRNA expression and decreased TFAM protein and mRNA levels compared with noncachectic COPD patients. In addition, PPAR-α mRNA levels in skeletal muscle correlated negatively with inflammatory markers in plasma. Therefore, a disturbed expression of these regulatory factors may well underlie the disturbed skeletal muscle functioning in chronic obstructive pulmonary disease.
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“Remels and colleagues observed low levels of peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC1-α, the master regulator of mitochondrial biogenesis) and its downstream effector, mitochondrial transcription factor A (TFAM), in COPD quadriceps; these differences were further enhanced in cachectic COPD patients [90].”
From Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting (2023) · cites this paper as [90]
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Cites
Transcriptional co-activator PGC-1α drives the formation of slow-twitch muscle fibres
Lin, J., Wu, H., Tarr, P. T., Zhang, C.-Y., Wu, Z., Boss, O., Michael, L. F., Puigserver, P., Isotani, E., Olson, E. N., et al. (2002) · Nature · doi:10.1038/nature00904 · Cited by 2,546
Puigserver, P., & Spiegelman, B. M. (2003) · Endocrine Reviews · doi:10.1210/er.2002-0012 · Cited by 2,076
Regulation of Muscle Fiber Type and Running Endurance by PPARδ
Wang, Y.-X., Zhang, C.-L., Yu, R. T., Cho, H. K., Nelson, M. C., Bayuga-Ocampo, C. R., Ham, J., Kang, H., & Evans, R. M. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020294 · Cited by 1,089
Emerging roles of PPARS in inflammation and immunity
Daynes, R. A., & Jones, D. C. (2002) · Nature reviews. Immunology · doi:10.1038/nri912 · Cited by 926
Marquis, K., Debigaré, R., Lacasse, Y., Leblanc, P., Jobin, J., Carrier, G., & Maltais, F. (2002) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.2107031 · Cited by 840
Invited Review: Contractile activity-induced mitochondrial biogenesis in skeletal muscle
Hood, D. A. (2001) · Journal of Applied Physiology · doi:10.1152/jappl.2001.90.3.1137 · Cited by 692
Statistical guidelines for contributors to medical journals.
Altman, D. G., Gore, S. M., Gardner, M. J., & Pocock, S. (1983) · BMJ · doi:10.1136/bmj.286.6376.1489 · Cited by 662
Peroxisome proliferator‐activated receptor δ controls muscle development and oxydative capability
Luquet, S., Lopez‐Soriano, J., Holst, D., Fredenrich, A., Melki, J., Rassoulzadegan, M., & Grimaldi, P. A. (2003) · The FASEB Journal · doi:10.1096/fj.03-0269fje · Cited by 509
Tumor Necrosis Factor-Alpha Levels and Weight Loss in Chronic Obstructive Pulmonary Disease
Di Francia, M., Barbier, D., Mège, J. L., & OREHEK, J. (1994) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.150.5.7952575 · Cited by 480
Koves, T. R., Li, P., An, J., Akimoto, T., Slentz, D., Ilkayeva, O., Dohm, G. L., Yan, Z., Newgard, C. B., & Muoio, D. M. (2005) · Journal of Biological Chemistry · doi:10.1074/jbc.m507621200 · Cited by 464
Research works printed but not linked: 1
- 10.1210/me.10.11.1457 · DOI
Cited by
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Systemic manifestations and comorbidities of COPD
Barnes, P. J., & Celli, B. R. (2009) · European Respiratory Journal · doi:10.1183/09031936.00128008 · Cited by 1,863
Maltais, F., Decramer, M., Casaburi, R. H., Barreiro, E., Burelle, Y., Debigaré, R., Dekhuijzen, P. N. R., Franssen, F. M. E., Gayan‐Ramirez, G., Gea, J., et al. (2014) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201402-0373st · Cited by 1,165
Self-citationMitochondrial Damage-Associated Molecular Patterns: From Inflammatory Signaling to Human Diseases
Grazioli, S., & Pugin, J. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.00832 · Cited by 429
Cloonan, S. M., & Choi, A. M. K. (2016) · Journal of Clinical Investigation · doi:10.1172/jci81113 · Cited by 322
Skeletal muscle dysfunction in patients with chronic obstructive pulmonary disease
Hussain, S., Cheol, K., & Mofarrahi, M. (2008) · International Journal of Chronic Obstructive Pulmonary Disease · doi:10.2147/copd.s4480 · Cited by 224
Ehrenborg, E., & Krook, A. (2009) · Pharmacological Reviews · doi:10.1124/pr.109.001560 · Cited by 222
The mechanisms of cachexia underlying muscle dysfunction in COPD
Remels, A. H. V., Gosker, H. R., LANGEN, R. C. J., & Schols, A. M. W. J. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00790.2012 · Cited by 181
Self-citationvan de Bool, C., Rutten, E. P. A., van Helvoort, A., Franssen, F. M. E., Wouters, E. F. �., & Schols, A. M. W. J. (2017) · Journal of Cachexia Sarcopenia and Muscle · doi:10.1002/jcsm.12219 · Cited by 145
Self-citationMuscle function in COPD: a complex interplay
Man, W. D., Donaldson, G. C., Maddocks, M. M., Martolini, & Polkey, M. I. (2012) · International Journal of COPD · doi:10.2147/copd.s28247 · Cited by 150
Skeletal muscle effects of electrostimulation after COPD exacerbation: a pilot study
Abdellaoui, A., Prefaut, C., Gouzi, F., Couillard, A., Coisy‐Quivy, M., Hugon, G., Molinari, N., Lafontaine, T., Jonquet, O., Laoudj‐Chenivesse, D., et al. (2011) · European Respiratory Journal · doi:10.1183/09031936.00167110 · Cited by 142
Tang, K., Wagner, P. D., & Breen, E. C. (2010) · Journal of Cellular Physiology · doi:10.1002/jcp.21955 · Cited by 125
“In the experiments presented in the current study, mice exposed to just 16 weeks of cigarette smoke reproduced many of the muscle abnormalities seen in humans (Jobin et al., 1998; Maltais et al., 1998; Whittom et al., 1998; Remels et al., 2007; Gosker et al., 2009).”
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Remels, A. H. V., Gosker, H. R., Schrauwen, P., Hommelberg, P. P. H., Sliwinski, P., Polkey, M., Galdiz, J., Wouters, E. F. M., Langen, R. C. J., & Schols, A. M. W. J. (2010) · The FASEB Journal · doi:10.1096/fj.09-150714 · Cited by 122
Self-citationvan den Borst, B., Slot, I. G. M., Hellwig, V. A. C. V., Vosse, B. A. H., KELDERS, M. C. J. M., Barreiro, E., Schols, A. M. W. J., & Gosker, H. R. (2012) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00508.2012 · Cited by 124
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Skeletal muscle dysfunction in COPD: clinical and laboratory observations
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Picard, M., Godin, R., Sinnreich, M., Baril, J., Bourbeau, J., Perrault, H., Taivassalo, T., & Burelle, Y. (2008) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.200807-1005oc · Cited by 95
Greulich, T., Nell, C., Koepke, J., Fechtel, J., Franke, M., Schmeck, B., Haid, D., Apelt, S., Filipovic, S., Kenn, K., et al. (2014) · BMC Pulmonary Medicine · doi:10.1186/1471-2466-14-60 · Cited by 94
Rabinovich, R., & Vilaró, J. (2010) · Current Opinion in Pulmonary Medicine · doi:10.1097/mcp.0b013e328336438d · Cited by 93
Shrikrishna, D., Astin, R., Kemp, P. R., & Hopkinson, N. S. (2012) · Clinical Science · doi:10.1042/cs20120081 · Cited by 92
Main Pathogenic Mechanisms and Recent Advances in COPD Peripheral Skeletal Muscle Wasting
Henrot, P., Dupin, I., Schilfarth, P., Esteves, P., Blervaque, L., Zysman, M., Gouzi, F., Hayot, M., Pomiès, P., & Berger, P. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076454 · Cited by 85
“Remels and colleagues observed low levels of peroxisome proliferator-activated receptor-gamma coactivator 1 alpha (PGC1-α, the master regulator of mitochondrial biogenesis) and its downstream effector, mitochondrial transcription factor A (TFAM), in COPD quadriceps; these differences were further enhanced in cachectic…”
BackgroundMolecular regulation of skeletal muscle mass
Russell, A. P. (2009) · Clinical and Experimental Pharmacology and Physiology · doi:10.1111/j.1440-1681.2009.05265.x · Cited by 80
Maddocks, M. M., Shrikrishna, D., Vitoriano, S., Natanek, S. A., Tanner, R., Hart, N., Kemp, P. R., Moxham, J., Polkey, M. I., & Hopkinson, N. S. (2014) · European Respiratory Journal · doi:10.1183/09031936.00066414 · Cited by 81
Meyer, A., Zoll, J., Charles, A. L., Charloux, A., de Blay, F., Diemunsch, P., Sibilia, J., Piquard, F., & Geny, B. (2013) · Experimental Physiology · doi:10.1113/expphysiol.2012.069468 · Cited by 90
Chaillou, T. (2018) · Frontiers in Physiology · doi:10.3389/fphys.2018.01450 · Cited by 80
New Therapies for Chronic Obstructive Pulmonary Disease
Barnes, P. J. (2010) · Medical Principles and Practice · doi:10.1159/000316368 · Cited by 78
Future Treatments for Chronic Obstructive Pulmonary Disease and Its Comorbidities
Barnes, P. J. (2008) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200807-069th · Cited by 78
MacMillan, N. J., Kapchinsky, S., Goddard, Y., Gouspillou, G., Sena, R. D. S., Jagoe, R. T., Baril, J., Carver, T. E., Andersen, R. E., Richard, R., et al. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00114 · Cited by 70
Comparative assessment of the quadriceps and the diaphragm in patients with COPD
Caron, M., Debigaré, R., Dekhuijzen, P. N. R., & Maltais, F. (2009) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00194.2009 · Cited by 69
Effects of exercise on mitochondrial DNA content in skeletal muscle of patients with COPD
Puente‐Maestu, L., Lázaro, A., Tejedor, A., Camaño, S., Fuentes, M., Cuervo, M., Navarro, B., & Agustí, A. G. N. (2010) · Thorax · doi:10.1136/thx.2010.153031 · Cited by 71
Peroxisome Proliferator-Activated Receptors as Novel Targets in Lung Disease *
Belvisi, M. G., & Hele, D. J. (2008) · CHEST Journal · doi:10.1378/chest.07-0019 · Cited by 66
Inactivation of glycogen synthase kinase-3β (GSK-3β) enhances skeletal muscle oxidative metabolism
Theeuwes, W. F., Gosker, H. R., LANGEN, R. C. J., Verhees, K. J. P., Pansters, N., Schols, A. M. W. J., & Remels, A. H. V. (2017) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2017.09.018 · Cited by 63
Self-citationRemels, A. H. V., Gosker, H. R., van der Velden, J. L. J., LANGEN, R. C. J., & Schols, A. M. W. J. (2007) · Clinics in Chest Medicine · doi:10.1016/j.ccm.2007.06.003 · Cited by 62
Self-citationSexually-dimorphic targeting of functionally-related genes in COPD
Glass, K., Quackenbush, J. F., Silverman, E. K., Celli, B. R., Rennard, S. I., Yuan, G., & DeMeo, D. L. (2014) · BMC Systems Biology · doi:10.1186/s12918-014-0118-y · Cited by 59
Exercise and muscle dysfunction in COPD: implications for pulmonary rehabilitation
Man, W. D., Kemp, P. R., Moxham, J., & Polkey, M. I. (2009) · Clinical Science · doi:10.1042/cs20080660 · Cited by 61
Castillero, E., Nieto‐Bona, M. P., Fernández‐Galaz, C., Martı́n, A. I., López-Menduiña, M., Granado, M., Villanúa, M. Á., & López‐Calderón, A. (2011) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00590.2010 · Cited by 59
Yin, Y., Hou, G., Li, E., Wang, Q., & Kang, J. (2014) · Respiratory Research · doi:10.1186/1465-9921-15-28 · Cited by 57
Measuring and monitoring skeletal muscle function in COPD: current perspectives
Marklund, S., Bui, K.-L., & Nyberg, A. (2019) · International Journal of COPD · doi:10.2147/copd.s178948 · Cited by 55
Aniwidyaningsih, W., Varraso, R., Cano, N., & Pison, C. (2008) · Current Opinion in Clinical Nutrition and Metabolic Care · doi:10.1097/mco.0b013e3283023d37 · Cited by 53
Functional crosstalk of PGC-1 coactivators and inflammation in skeletal muscle pathophysiology
Eisele, P. S., & Handschin, C. (2013) · Seminars in Immunopathology · doi:10.1007/s00281-013-0406-4 · Cited by 54
Leermakers, P. A., Schols, A. M. W. J., Kneppers, A. E. M., Kelders, M. C. J. M., de Theije, C. C., Lainscak, M., & Gosker, H. R. (2018) · Scientific Reports · doi:10.1038/s41598-018-33471-2 · Cited by 53
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Taivassalo, T., & Hussain, S. N. A. (2016) · Chest · doi:10.1016/j.chest.2015.11.021 · Cited by 59
Altered mitochondrial regulation in quadriceps muscles of patients with COPD
Naimi, A. I., Bourbeau, J., Perrault, H., Baril, J., Wright‐Paradis, C., Rossi, A. M., Taivassalo, T., Sheel, A. W., Rabøl, R., Dela, F., et al. (2010) · Clinical Physiology and Functional Imaging · doi:10.1111/j.1475-097x.2010.00988.x · Cited by 51
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Nam, H.-S., Izumchenko, E., Dasgupta, S., & Hoque, M. O. (2017) · Biomarkers in Medicine · doi:10.2217/bmm-2016-0373 · Cited by 52
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Zhang, L., Valizadeh, H., Alipourfard, I., Bidares, R., Maleki, L. A., & Ahmadi, M. (2020) · COPD Journal of Chronic Obstructive Pulmonary Disease · doi:10.1080/15412555.2020.1780576 · Cited by 51
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Self-citationSkeletal Muscle Dysfunction in Patients with Chronic Obstructive Pulmonary Disease
Kim, H. C., Lee, G. D., & Hwang, Y. S. (2010) · Tuberculosis & respiratory diseases · doi:10.4046/trd.2010.68.3.125 · Cited by 50
Salazar‐Degracia, A., Busquets, S., Argilés, J. M. A., Bargalló-Gispert, N., López-Soriano, F. J., & Barreiro, E. (2018) · Biochimie · doi:10.1016/j.biochi.2018.04.009 · Cited by 50
Resveratrol and metabolic health in COPD: A proof-of-concept randomized controlled trial
Beijers, R. J. H. C. G., Gosker, H. R., Sanders, K. J. C., de Theije, C. C., KELDERS, M. C. J. M., Clarke, G. A., Cryan, J. F., van den Borst, B., & Schols, A. M. W. J. (2020) · Clinical Nutrition · doi:10.1016/j.clnu.2020.01.002 · Cited by 48
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Wang, M., Xie, Z., Xu, J., & Feng, Z. (2020) · Clinica Chimica Acta · doi:10.1016/j.cca.2020.06.007 · Cited by 46
Konokhova, Y., Spendiff, S., Jagoe, R. T., Aare, S., Kapchinsky, S., MacMillan, N. J., Rozakis, P., Picard, M., Aubertin-Leheudre, M., Pion, C. H., et al. (2016) · Skeletal Muscle · doi:10.1186/s13395-016-0083-9 · Cited by 46
Locomotor Muscles in COPD: The Rationale for Rehabilitative Exercise Training
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Frontrunners in novel pharmacotherapy of COPD
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Current views in chronic obstructive pulmonary disease pathogenesis and management
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Wang, J., Wang, F., Zhang, P., Liu, H., He, J., Zhang, C., Fan, M., & Chen, X. (2016) · Bioscience Biotechnology and Biochemistry · doi:10.1080/09168451.2016.1254531 · Cited by 43
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Slot, I. G. M., Schols, A. M. W. J., Vosse, B. A. H., KELDERS, M. C. J. M., & Gosker, H. R. (2014) · Cellular Signalling · doi:10.1016/j.cellsig.2014.04.016 · Cited by 46
Self-citationChacon‐Cabrera, A., Lund‐Palau, H., Gea, J., & Barreiro, E. (2016) · PLoS ONE · doi:10.1371/journal.pone.0164951 · Cited by 42
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Self-citationWang, Y., Li, P., Cao, Y., Liu, C., Wang, J., & Wu, W. (2022) · Aging and Disease · doi:10.14336/ad.2022.0603 · Cited by 41
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Mitochondrial biology in airway pathogenesis and the role of NRF2
Cho, H., & Kleeberger, S. R. (2019) · Archives of Pharmacal Research · doi:10.1007/s12272-019-01182-5 · Cited by 39
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Becker, J., Delayre‐Orthez, C., Frossard, N., & Pons, F. (2007) · Pulmonary Pharmacology & Therapeutics · doi:10.1016/j.pupt.2007.08.001 · Cited by 35
Hoeks, J., Arany, Z. P., Phielix, E., Moonen‐Kornips, E., Hesselink, M. K. C., & Schrauwen, P. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.22812 · Cited by 36
Self-citationGreulich, T., Kehr, K., Nell, C., Koepke, J., Haid, D., Koehler, U., Koehler, K., Filipovic, S., Kenn, K., Vogelmeier, C. F., et al. (2014) · Respiratory Research · doi:10.1186/1465-9921-15-36 · Cited by 34
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Self-citationPeng, H., Yang, M. H., Chen, Z.-Y., Chen, P., Guan, C., Xiang, X.-D., Cai, S., Chen, Y., & Fang, X. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082739 · Cited by 34
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Metadata
- Authors
- Remels, A. H., Schrauwen, P., Broekhuizen, R., Willems, J., Kersten, S., Gosker, H. R., & Schols, A. M.
- Affiliations
- Maastricht University (NL)
- Venue
- European Respiratory Journal
- Publisher
- European Respiratory Society (ERS)
- Published
- 2007-04-25
- Volume
- 30
- Issue
- 2
- Pages
- 245-252
- ISSN
- 0903-1936 (ISSN-L)
- 1399-3003
- OpenAlex
- W2137507155
- Cited by
- 168
- References
- 35
- Citations by year
- 2026: 2 · 2025: 8 · 2024: 1 · 2023: 2 · 2022: 5 · 2021: 4 · 2020: 13 · 2019: 9 · 2018: 8 · 2017: 12 · 2016: 12 · 2015: 6 · 2014: 12 · 2013: 14 · 2012: 10
- FWCI
- 4.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- European Respiratory Journal (publishedVersion)
- PubMed (publishedVersion)
- Research Publications (Maastricht University) (publishedVersion, other-oa)
- Socio-Environmental Systems Modeling (submittedVersion)
- Research Publications (Maastricht University) (submittedVersion, other-oa)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Muscle Physiology and Disorders
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Chronic Obstructive Pulmonary Disease (COPD) Research
- Health Sciences › Medicine › Physiology (medical) › Nutrition and Health in Aging
- Keywords
- chronic obstructive pulmonary disease, skeletal muscle, cachexia, PPARγ, PPARδ, PPARα, PGC-1α, TFAM, mitochondrial biogenesis, muscle weakness, systemic inflammation, gene expression
- MeSH terms
- Aged, Analysis of Variance, Body Composition, DNA-Binding Proteins, Enzyme-Linked Immunosorbent Assay, Female, Humans, Male, Middle Aged, Phenotype, Respiratory Function Tests, Transcription Factors, Tumor Necrosis Factor-alpha, Blotting, Western, Case-Control Studies, Muscle, Skeletal, Reverse Transcriptase Polymerase Chain Reaction, Mitochondrial Proteins, Pulmonary Disease, Chronic Obstructive, Peroxisome Proliferator-Activated Receptors
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