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Exposure to cigaret...
Exposure to cigarette smoke induces overexpression of von Hippel-Lindau tumor suppressor in mouse skeletal muscle
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- Basic, Vladimir Tomislav (författare)
- Department of Clinical Medicine, Örebro University, Örebro, Sweden
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- Tadele, Elsa (författare)
- Department of Clinical Medicine, Örebro University, Örebro, Sweden
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- Elmabsout, Ali Ateia (författare)
- Department of Clinical Medicine, Örebro University, Örebro, Sweden
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- Yao, Hongwei (författare)
- Department of Environmental Medicine, Lung Biology and Disease Program, University of Rochester Medical Center, Rochester NY, USA
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- Rahman, Irfan (författare)
- Department of Environmental Medicine, Lung Biology and Disease Program, University of Rochester Medical Center, Rochester NY, USA
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- Sirsjö, Allan, 1959- (författare)
- Örebro universitet,Institutionen för hälsovetenskap och medicin
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- Abdel-Halim, Samy M., 1961- (författare)
- Department of Environmental Medicine, Lung Biology and Disease Program, University of Rochester Medical Center, Rochester NY, USA
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(creator_code:org_t)
- Bethesda, USA : American Physiological Society, 2012
- 2012
- Engelska.
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Ingår i: American Journal of Physiology - Lung cellular and Molecular Physiology. - Bethesda, USA : American Physiological Society. - 1040-0605 .- 1522-1504. ; 303:6, s. L519-L527
- Relaterad länk:
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https://doi.org/10.1...
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https://europepmc.or...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Cigarette smoke (CS) is a well established risk factor in the development of chronic obstructive pulmonary disease (COPD). In contrast, the extent to which CS exposure contributes to the development of the systemic manifestations of COPD, such as skeletal muscle dysfunction and wasting remains largely unknown. Decreased skeletal muscle capillarization has been previously reported in early stages of COPD and might play an important role in the development of COPD-associated skeletal muscle abnormalities. To investigate the effects of chronic CS exposure on skeletal muscle capillarization and exercise tolerance a mouse model of CS exposure was used. The129/SvJ mice were exposed to CS for 6 months, and the expression of putative elements of the hypoxia-angiogenic signaling cascade as well as muscle capillarization were studied. Additionally, functional tests assessing exercise tolerance/endurance were performed in mice. Compared to controls, skeletal muscles from CS-exposed mice exhibited significantly enhanced expression of von Hippel-Lindau tumor suppressor (VHL), ubiquitin-conjugating enzyme E2D1 (UBE2D1) and prolyl hydroxylase-2 (PHD2). In contrast, hypoxia-inducible factor-1 (HIF1-α) and vascular endothelial growth factor (VEGF) expression was reduced. Furthermore, reduced muscle fiber cross-sectional area, decreased skeletal muscle capillarization, and reduced exercise tolerance were also observed in CS-exposed animals. Taken together, the current results provide evidence linking chronic CS exposure and induction of VHL expression in skeletal muscles leading towards impaired hypoxia-angiogenesis signal transduction, reduced muscle fiber cross-sectional area and decreased exercise tolerance.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Hälsovetenskap -- Sjukgymnastik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Health Sciences -- Physiotherapy (hsv//eng)
Nyckelord
- Capillaries
- chronic obstructive pulmonary disease
- hypoxia inducible factor-1 alpha
- pulmonary cachexia syndrome
- vascular endothelial growth factor
- Biomedicin
- Biomedicine
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
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