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dc.contributor.authorMAASS, Anne
dc.contributor.authorDUEZEL, Sandra
dc.contributor.authorBRIGADSKI, Tanja
dc.contributor.authorGOERKE, Monique
dc.contributor.authorBECKE, Andreas
dc.contributor.authorSOBIERAY, Uwe
dc.contributor.authorNEUMANN, Katja
dc.contributor.authorLOVDEN, Martin
dc.contributor.authorLINDENBERGER, Ulman
dc.contributor.authorBACKMAN, Lars
dc.contributor.authorBRAUN-DULLAEUS, Ruediger
dc.contributor.authorAHRENS, Doerte
dc.contributor.authorHEINZE, Hans-Jochen
dc.contributor.authorMUELLER, Notger G.
dc.contributor.authorLESSMANN, Volkmar
dc.contributor.authorSENDTNER, Michael
dc.contributor.authorDUEZEL, Emrah
dc.date.accessioned2019-03-01T14:53:15Z
dc.date.available2019-03-01T14:53:15Z
dc.date.issued2016
dc.identifier.citationNeuroimage, 2016, Vol. 131, pp. 142-154
dc.identifier.issn1053-8119
dc.identifier.issn1095-9572en
dc.identifier.urihttps://hdl.handle.net/1814/61443
dc.descriptionPublished: May 2016
dc.description.abstractAnimal models point towards a key role of brain-derived neurotrophic factor (BDNF), insulin-like growth factor-I (IGF-I) and vascular endothelial growth factor (VEGF) in mediating exercise-induced structural and functional changes in the hippocampus. Recently, also platelet derived growth factor-C (PDGF-C) has been shown to promote blood vessel growth and neuronal survival. Moreover, reductions of these neurotrophic and angiogenic factors in old age have been related to hippocampal atrophy, decreased vascularization and cognitive decline. In a 3-month aerobic exercise study, forty healthy older humans (60 to 77 years) were pseudo-randomly assigned to either an aerobic exercise group (indoor treadmill, n=21) or to a control group (indoor progressive-muscle relaxation/stretching, n=19). As reported recently, we found evidence for fitness-related perfusion changes of the aged human hippocampus that were closely linked to changes in episodic memory function. Here, we test whether peripheral levels of BDNF, IGF-I, VEGF or PDGF-C are related to changes in hippocampal blood flow, volume and memory performance. Growth factor levels were not significantly affected by exercise, and their changes were not related to changes in fitness or perfusion. However, changes in IGF-I levels were positively correlated with hippocampal volume changes (derived by manual volumetry and voxel-based morphometry) and late verbal recall performance, a relationship that seemed to be independent of fitness, perfusion or their changes over time. These preliminary findings link IGF-I levels to hippocampal volume changes and putatively hippocampus-dependent memory changes that seem to occur over time independently of exercise. We discuss methodological shortcomings of our study and potential differences in the temporal dynamics of how IGF-1, VEGF and BDNF may be affected by exercise and to what extent these differences may have led to the negative findings reported here. (C) 2015 The Authors. Published by Elsevier Inc.
dc.description.sponsorshipGerman Center for Neurodegenerative Diseases
dc.description.sponsorshipOtto-von-Guericke University (IKND)
dc.description.sponsorshipSwedish Research Council Formas
dc.description.sponsorshipSwedish Research Council for Health, Working Life, and Welfare
dc.description.sponsorshipSwedish Brain Power, an Alexander von Humboldt Research Award
dc.format.mimetypeapplication/pdf
dc.language.isoen
dc.publisherElsevieren
dc.relation.ispartofNeuroimage
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectExercise
dc.subjectNeurotrophic factors
dc.subjectHippocampus
dc.subjectVascular plasticity
dc.subjectAging
dc.subjectGrowth-factor-Ien
dc.subjectNeurotrophic factoren
dc.subjectPhysical-exerciseen
dc.subjectVal66met polymorphismen
dc.subjectVoluntary exerciseen
dc.subjectBrain plasticityen
dc.subjectAlpha-receptoren
dc.subjectPdgf-Ccen
dc.subjectNeurogenesisen
dc.subjectIncreasesen
dc.titleRelationships of peripheral IGF-1, VEGF and BDNF levels to exercise-related changes in memory, hippocampal perfusion and volumes in older adults
dc.typeArticle
dc.identifier.doi10.1016/j.neuroimage.2015.10.084
dc.identifier.volume131
dc.identifier.startpage142
dc.identifier.endpage154
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dc.rights.licenseCreative Commons CC BY-NC-ND 4.0


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