The DOI matches its Crossref record.
Angiogenic growth factor mRNA responses in muscle to a single bout of exercise
Abstract
A major adaptation to exercise is new capillary formation in skeletal muscle. On the basis of angiogenesis in tumors and during development, several angiogenic growth factors may be involved, including vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), and transforming growth factor-beta 1 (TGF-beta 1). In 9-wk-old female Wistar rats, mRNA expression for these three growth factors in gastrocnemius muscle was examined by quantitative Northern analysis after a single 1-h run at 15 or 20 m/min at 10 degrees incline in room air. A third group ran at 15 m/min in 12% O2, and resting control groups were included at inspired O2 fractions of 0.21 and 0.12. Exercise significantly increased mRNA levels two- to fourfold, which was evident over the first 4 h postexercise; by 8 and 24 h, mRNA levels returned to baseline. For all three factors, mRNA levels were significantly higher after exercise at 20 than at 15 m/min. Hypoxia at rest doubled VEGF and TGF-beta 1 message but had no effect on bFGF. Hypoxic exercise further raised VEGF mRNA levels but had no effect on the other factors. We suggest that VEGF, bFGF, and TGF-beta 1 may be involved in the angiogenic response to exercise and that reduced intracellular PO2 (as occurs during normoxic exercise) may be part of the stimulus to such growth factor production.
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“This paper demonstrated that a single bout of exercise can increase VEGF1 and TGFβ1 expression in muscle to promote the angiogenic response to exercise.”
From Exerkines in health, resilience and disease (2022) · cites this paper as [198]
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BackgroundResultInfluentialSelf-citationExercise stimulates neovascularization in occluded muscle without affecting bFGF content
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Kim, J., Yoon, D. H., Kim, H., Choi, M., & Song, W. J. (2016) · Integrative Medicine Research · doi:10.1016/j.imr.2016.05.001 · Cited by 22
Dai, Q., Thompson, M. A., Pippen, A. M., et al. (2002) · Vascular Medicine · doi:10.1191/1358863x02vm430oa · Cited by 20
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BackgroundGustafsson, T. P., & Sundberg, C. J. (2000) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2000.279.6.h3146 · Cited by 18
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Suzuki, J. (2004) · Acta Physiologica Scandinavica · doi:10.1111/j.1365-201x.2004.01279.x · Cited by 17
Green, H. J., Burnett, M., Kollias, H., Ouyang, J., Smith, I. C. P., & Tupling, S. (2012) · Canadian Journal of Physiology and Pharmacology · doi:10.1139/y2012-013 · Cited by 15
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Suzuki, J. (2002) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.52.409 · Cited by 14
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BackgroundVascular-Specific Growth Factor mRNA Levels in the Human Diaphragm
Alexopoulou, C., Mitrouska, I., Arvanitis, D. A., Tzanakis, Ν., Chalkiadakis, G., Melissas, J., Zervou, M. I., & Siafakas, N. M. (2005) · Respiration · doi:10.1159/000089580 · Cited by 11
Effect of neonatal surfactant therapy on lung function at school age in children born very preterm
Pelkonen, A. S., Hakulinen, A., Turpeinen, M., & Hallman, M. (1998) · Pediatric Pulmonology · doi:10.1002/(sici)1099-0496(199803)25:3 · Cited by 46
Gustafsson, T. P., PUNTSCHART, Sundberg, C. J., et al. (1999) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.1999.00515.x · Cited by 10
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Elia, A., & Lemaître, F. (2025) · European Journal of Applied Physiology · doi:10.1007/s00421-025-05752-y · Cited by 12
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Al-Horani, R., Al‐Trad, B., & Haifawi, S. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00918.2018 · Cited by 8
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Flora, R., Freisleben, H., Ferdinal, F., et al. (2012) · Medical Journal of Indonesia · doi:10.13181/mji.v21i3.493 · Cited by 6
Elchaninova, S. A., Korenyak, N. A., Pavlovskaya, L. I., et al. (2004) · Human Physiology · doi:10.1023/b:hump.0000049591.78738.55 · Cited by 6
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Song, K., Cho, H.-W., Lee, H.-K., & Cho, B. W. (2014) · Asian-Australasian Journal of Animal Sciences · doi:10.5713/ajas.2013.13821 · Cited by 4
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Vega, S. R., Hollmann, W., & Strüder, H. K. (2012) · Springer eBooks · doi:10.1007/978-1-4614-3293-7_8 · Cited by 3
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Menzies, K. J., Zaldivar‐Jolissaint, J. F., & Auwerx, J. H. (2016) · Springer eBooks · doi:10.1007/978-94-024-0962-8_9 · Cited by 2
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HUDLICKÁ, O., & Brown, M. D. (1999) · Springer eBooks · doi:10.1007/978-3-662-03776-8_6 · Cited by 2
Maasar, M., Turner, D., Gorski, P., Seaborne, R. A., Strauss, J., Shepherd, S., Cocks, M., Pillon, N. J., Zierath, J., Hulton, A., et al. (2020) · bioRxiv · doi:10.1101/2020.09.11.292805 · Cited by 3
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Yan, Z., Okutsu, M., Akhtar, Y., Lira, V. A., Lambert, B. S., Shimkus, K. L., Fluckey, J. D., Riechman, S. E., Bannai, M., Ohyama, K., et al. (2011) · Cited by 1
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Simonson, T. S. (2019) · CHEST Journal · doi:10.1016/j.chest.2018.09.029 · Cited by 1
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Anton, J. E. (2010) · TigerPrints (Clemson University)
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Kwak, H. B. (2008) · OakTrust (Texas A&M University Libraries)
Groover, A. L. (2014) · KU ScholarWorks (University of Kansas)
Patel, A. N., & Genovese, J. A. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-272-4_17
Cotter, E. J. (2005) · Dublin City University Open Access Institutional Repository (Dublin City University)
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Flora, R., Zulkarnain, M., Ardi, Y., Sorena, E., Wati, R., Wena, S., Juliansyah, R. A., & Slamet, S. (2015) · International Journal of Public Health Science (IJPHS) · doi:10.11591/ijphs.v4i3.4734
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Suzuki, J. (2013) · The Journal of Physical Fitness and Sports Medicine · doi:10.7600/jpfsm.2.237
Pilania, N. (2011) · doi:10.31274/etd-180810-1976
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BackgroundRole of vascular plasticity in muscle remodeling in the child
Gitiaux, C. (2015) · theses.fr (ABES) · doi:10.70675/6a10c0d4z3afaz49efza017z843ffa5759f2
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Banek, C. T. (2014) · Scholars' Bank (University of Oregon)
Prior, B. M., Yang, H. T., Terjung, R. L., Raue, U., Jemioło, B., Yang, Y., Trappe, S. W., Wiley, M. M., Muthukumar, V., Griffin, T. M., et al. (2015)
Benoît, H., Wagner, P. D., Gavin, T. P., et al. (2015)
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Bartłomiejczyk, I., & Przybylski, J. (2006)
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Innere, A., Pädiatrie, A., Direktor, Ä., et al. (2007)
Minier, S. L. (2004) · Research Exchange (Washington State University)
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Heinemeier, K. M., Langberg, H., Olesen, J. L., Kjær, M., Sun, Y., Thoreson, A. R., Stephen, S., Zhao, C., An, K., Peter, C. T., et al. (2011)
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Peters, K. G., Kraus, W. E., Annex, B. H., et al. (2016)
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Liu, S. T. K. (2014) · YorkSpace (York University)
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Grano, M., & Colaianni, G. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.11218-8
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Addinsall, A. B. (2018) · Own your potential (DEAKIN)
Yau, S., Patten, A. R., Sharp, Z., & Christie, B. R. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801977-1.00005-2
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Joo, B. S., Son, J., Park, M. J., Joo, J. K., Kim, C. W., & Lee, K.-S. (2017) · Clinical and Experimental Obstetrics & Gynecology · doi:10.12891/ceog3491.2017
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Stary, C. M. (2006) · eScholarship (California Digital Library)
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“Its expression can be induced in a wide variety of cell types and tissues [143], including muscle fibers [144, 145], myofibroblasts [146], endothelial cells [119, 147], and vascular smooth muscle cells [132].”
Metadata
- Authors
- Breen, E. C., Johnson, E. C., Wagner, H., Tseng, H. M., Sung, L. A., & Wagner, P. D.
- Affiliations
- University of California San Diego (US)
- Venue
- Journal of Applied Physiology
- Publisher
- American Physiological Society
- Published
- 1996-07-01
- Volume
- 81
- Issue
- 1
- Pages
- 355-361
- ISSN
- 0161-7567 (ISSN-L)
- 8750-7587
- 1522-1601
- OpenAlex
- W2137609684
- Cited by
- 302
- References
- 0
- Citations by year
- 2026: 3 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 5 · 2021: 8 · 2020: 7 · 2019: 6 · 2018: 5 · 2017: 5 · 2016: 15 · 2015: 21 · 2014: 13 · 2013: 13 · 2012: 13
- FWCI
- 22.86
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Applied Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health (5r01hl046910-04)
- National Heart, Lung, and Blood Institute (P01HL017731, 2-PO1-HL-17731, 5-RO1-HL-46910)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Health Sciences › Medicine › Physiology (medical) › Exercise and Physiological Responses
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Keywords
- exercise-induced angiogenesis, angiogenic factors, vascular endothelial growth factor, basic fibroblast growth factor, TGF-β1, hypoxic exercise, hypoxia, intracellular oxygen tension, mRNA expression, gastrocnemius, single bout exercise
- MeSH terms
- Animals, Hypoxia, Physical Exertion, Female, Half-Life, RNA, Messenger, Blotting, Northern, Transforming Growth Factor beta, Fibroblast Growth Factor 2, Endothelial Growth Factors, Rats, Wistar, In Situ Hybridization, Muscle, Skeletal, Rats
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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