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dc.contributor.authorStunes, Astrid Kamilla
dc.contributor.authorErben, Reinhold G.
dc.contributor.authorSchüler, Christiane
dc.contributor.authorEriksen, Erik Fink
dc.contributor.authorTice, Matthew
dc.contributor.authorVashishth, Deepak
dc.contributor.authorSyversen, Unni
dc.contributor.authorMosti, Mats Peder
dc.date.accessioned2020-01-30T07:14:58Z
dc.date.available2020-01-30T07:14:58Z
dc.date.created2020-01-13T13:38:07Z
dc.date.issued2019
dc.identifier.citationBone. 2020, 132nb_NO
dc.identifier.issn8756-3282
dc.identifier.urihttp://hdl.handle.net/11250/2638714
dc.description.abstractEstrogen deficiency causes bone loss and skeletal muscle dysfunction, and attenuates the musculoskeletal effects of exercise. The anti-diabetic drug metformin has been suggested to promote beneficial skeletal effects. To explore whether metformin can improve musculoskeletal training response during estrogen deficiency, we investigated the skeletal effects of plyometric exercise and metformin, in an ovarectomized (OVX) rat model of osteoporosis. Female Sprague Dawley rats, 12 weeks of age, rats were allocated to a sham-operated group (Sham), and four OVX groups; metformin (OVX-Met), exercise (OVX-Ex), combined metformin and exercise (OVX-MetEx) and a control group (OVX-Ctr), n = 12/group. Dual X-ray absorptiometry, micro computed tomography, fracture toughness testing, histomorphometry and plasma analyses were performed to explore skeletal effects. All intervention groups exhibited a higher gain in femoral bone mineral density (BMD) than OVX-Ctr (p < .01). The combined intervention also resulted in a higher gain in femoral and spine BMD compared to OVX-Met (p < .01). Both exercise groups displayed improved microarchitecture, including both cortical and trabecular parameters (p < .05). This was most evident in the OVX-MetEx group where several indices were at sham level or superior to OVX-Ctr (p < .05). The OVX-MetEx group also exhibited an enhanced toughening effect compared to the other OVX groups (p < .05). The beneficial skeletal effects seemed to be mediated by inhibition of bone resorption and stimulation of bone formation. The training response (i.e. jumping height) was also greater in the metformin treated rats compared to OVX-Ex (p < .01), indicating a performance-enhancing effect of metformin. Both exercise groups displayed higher lean mass than OVX-Ctr (p < .05). In conclusion, the combination of plyometric exercise and metformin improved trabecular microarchitecture and bone material properties relative to OVX controls. However, no additive effect of the combined intervention was observed compared to exercise alone.nb_NO
dc.language.isoengnb_NO
dc.publisherElseviernb_NO
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleSkeletal effects of plyometric exercise and metformin in ovariectomized ratsnb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionpublishedVersionnb_NO
dc.source.volume132nb_NO
dc.source.journalBonenb_NO
dc.identifier.doi10.1016/j.bone.2019.115193
dc.identifier.cristin1771477
dc.description.localcodeThis is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.nb_NO
cristin.unitcode1920,0,0,0
cristin.unitcode194,65,15,0
cristin.unitcode1920,15,0,0
cristin.unitnameSt. Olavs Hospital HF
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.unitnameMedisinsk klinikk
cristin.ispublishedtrue
cristin.qualitycode1


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