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dc.contributor.authorKivelä, Riikka
dc.contributor.authorSilvennoinen, Mika
dc.contributor.authorLehti, Maarit
dc.contributor.authorJalava, Sanni
dc.contributor.authorVihko, Veikko
dc.contributor.authorKainulainen, Heikki
dc.date.accessioned2012-11-20T11:57:25Z
dc.date.available2012-11-20T11:57:25Z
dc.date.issued2008-05-01fi
dc.identifier.citationKivelä, R., Silvennoinen, M., Lehti, M., Jalava, S., Vihko, V., & Kainulainen, H. (2008). Exercise-induced expression of angiogenic growth factors in skeletal muscle and in capillaries of healthy and diabetic mice. Cardiovascular Diabetology, 7 (13). Retrieved from http://www.cardiab.com/content/7/1/13fi
dc.identifier.urihttp://dx.doi.org/10.1186/1475-2840-7-13
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/40383
dc.description.abstractBackground. Diabetes has negative, and exercise training positive, effects on the skeletal muscle vasculature, but the mechanisms are not yet fully understood. In the present experiment the effects of running exercise on the mRNA expression of pro- and antiangiogenic factors were studied in healthy and diabetic skeletal muscle. The responses in capillaries and muscle fibers, collected from the muscle with laser capture microdissection, were also studied separately. Methods. Healthy and streptozotocin-induced diabetic mice were divided into sedentary and exercise groups. Exercise was a single bout of 1 h running on a treadmill. Gastrocnemius muscles were harvested 3 h and 6 h post exercise, and angiogenesis-related gene expressions were analyzed with real-time PCR. In addition to muscle homogenates, capillaries and muscle fibers were collected from the muscle with laser capture microdissection method and analyzed for vascular endothelial growth factor-A (VEGF-A) and thrombospondin-1 (TSP-1) mRNA expression. Results. Of the proangiogenic factors, VEGF-A and VEGF receptor-2 (VEGFR-2) mRNA expression increased significantly (P < 0.05) in healthy skeletal muscle 6 h post exercise. VEGF-B also showed a similar trend (P = 0.08). No significant change was observed post exercise in diabetic muscles in the expression of VEGF-A, VEGFR-2 or VEGF-B. The expression of angiogenesis inhibitor TSP-1 and angiogenic extracellular matrix protein Cyr61 were significantly increased in diabetic muscles (P < 0.05–0.01). Capillary mRNA expression resembled that in the muscle homogenates, however, the responses were greater in capillaries compared to muscle homogenates and pure muscle fibers. Conclusion. The present study is the first to report the effects of a single bout of exercise on the expression of pro- and antiangiogenic factors in diabetic skeletal muscle, and it provides novel data about the separate responses in capillaries and muscle fibers to exercise and diabetes. Diabetic mice seem to have lower angiogenic responses to exercise compared to healthy mice, and they show markedly increased expression of angiogenesis inhibitor TSP-1. Furthermore, exercise-induced VEGF-A expression was shown to be greater in capillaries than in muscle fibers.fi
dc.language.isoeng
dc.publisherBioMed Central (BMC)
dc.relation.ispartofseriesCardiovascular Diabetology
dc.subject.otherdiabetes
dc.subject.otherkapillaari
dc.subject.otherliikunta
dc.subject.othergeeniekspressio
dc.titleExercise-induced expression of angiogenic growth factors in skeletal muscle and in capillaries of healthy and diabetic micefi
dc.typeArticle
dc.identifier.urnURN:NBN:fi:jyu-201804202287
dc.contributor.laitosLiikuntabiologian laitosfi
dc.contributor.laitosDepartment of Biology of Physical Activityen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.identifier.doi10.1186/1475-2840-7-13
dc.date.updated2012-11-15T14:54:25Z
dc.rights.holderRiikka Kivelä et al.; licensee BioMed Central Ltd.
dc.type.coarjournal article
dc.description.reviewstatuspeerReviewed
dc.relation.issn1471-2148
dc.type.versionpublishedVersion
dc.rights.copyright© 2008 Kivelä et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
dc.rights.accesslevelopenAccessfi
dc.rights.urlhttp://creativecommons.org/licenses/by/2.0


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