Näytä suppeat kuvailutiedot

dc.contributor.advisorKainulainen, Heikki
dc.contributor.advisorFachada, Vasco
dc.contributor.authorAdeniran, Ajani Anuoluwapo
dc.date.accessioned2018-06-08T10:50:14Z
dc.date.available2018-06-08T10:50:14Z
dc.date.issued2018
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/58468
dc.description.abstractLow exercise capacity has been identified as a stronger predictor of morbidity and mortality relative to other commonly reported risk factors. Substrate metabolism, especially lipid storage, lipolysis and transportation in the skeletal muscles is strongly linked to aerobic capacity. The physical topographical properties of some myocellular particles and or organelles such mitochondria, lipid droplets (LDs) and perilipine-5 (Plin5) proteins in the skeletal muscle tissues have been implicated in the onset of most metabolic diseases and may also predict overall physical capacity. We tested the effect of innate high aerobic capacity (genetics) and acquired aerobic capacity (voluntary running) on the number, location and colocalization of the aforementioned particles in the gastrocnemius muscle cells, between the low and high capacity runner rats. Muscle samples from the gastrocnemius muscle of the specially bred rat model with high aerobic capacity (HCR) (n=20) and low aerobic capacity (LCR) (n=20) were used in this study. The samples were obtained from 4 equal subgroups; high capacity runner control (HCR-C) (n=10), high capacity runner receiving exercise intervention (HCR-R) (n=10), low capacity runner control (LCR-C) (n=10) and low capacity runner receiving exercise intervention (LCR-R) (n=10). Immunocytochemistry, confocal microscopy and bioinformatics were used in data collections and analysis. A one-way between subject analysis of variance (ANOVA) show statistically significant difference in the content of mitochondria (F (3,24) = 4.24, p<.0.05) and PLIN5 particles (F (3,24) = 3.8, p<.005). There were no significant differences in the number of LD (F (3,24) = 0.43, p>0.05) or in the colocalization of the LD and PLIN5 particles (F (3,24) = 1.2, p>.005) and LD and COXIV particles (F (3,24) = 1, p>.005) across the groups. The result suggests a strong interplay between genetic background and exercise stimulus. These factors may influence the skeletal muscle properties at the cellular level, effect of which may not only affect performance component but also health component of physical fitness. Physical activity may, however, enhance the cellular function or reverse genetic lags in cellular properties.en
dc.format.extent63
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.subject.othergenetics
dc.subject.otherlipid droplet
dc.subject.othercolocalization
dc.subject.otherphysical activity
dc.subject.othermetabolism
dc.titleEffects of exercise and genetics on skeletal muscle lipid metabolism with focus on the localization and association of lipid droplets, mitochondria ja PLIN5
dc.identifier.urnURN:NBN:fi:jyu-201806083123
dc.type.ontasotPro gradu -tutkielmafi
dc.type.ontasotMaster’s thesisen
dc.contributor.tiedekuntaLiikuntatieteellinen tiedekuntafi
dc.contributor.tiedekuntaFaculty of Sport and Health Sciencesen
dc.contributor.laitosLiikunta- ja terveystieteetfi
dc.contributor.laitosSport and Health Sciencesen
dc.contributor.yliopistoJyväskylän yliopistofi
dc.contributor.yliopistoUniversity of Jyväskyläen
dc.contributor.oppiaineLiikuntafysiologiafi
dc.contributor.oppiaineExercise Physiologyen
dc.rights.copyrightJulkaisu on tekijänoikeussäännösten alainen. Teosta voi lukea ja tulostaa henkilökohtaista käyttöä varten. Käyttö kaupallisiin tarkoituksiin on kielletty.fi
dc.rights.copyrightThis publication is copyrighted. You may download, display and print it for Your own personal use. Commercial use is prohibited.en
dc.type.publicationmasterThesis
dc.contributor.oppiainekoodi5011
dc.subject.ysogeneettiset tekijät
dc.subject.ysoaineenvaihdunta
dc.subject.ysofyysinen aktiivisuus
dc.subject.ysogenetic factors
dc.subject.ysometabolism
dc.subject.ysophysical activeness
dc.format.contentfulltext
dc.type.okmG2


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