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dc.contributor.authorDeveci, S.Ş.
dc.contributor.authorMatur, Z.
dc.contributor.authorKesim, Y.Y.
dc.contributor.authorSenturk (Şentürk), G.G.
dc.contributor.authorSargın-Kurt, G.G.
dc.contributor.authorUgur (Uğur), S.A.
dc.contributor.authorOge (Öge), A.E.
dc.date.accessioned2020-12-02T18:00:10Z
dc.date.available2020-12-02T18:00:10Z
dc.date.issued2020
dc.identifier.issn0006-8993
dc.identifier.urihttps://doi.org/10.1016/j.brainres.2020.146652
dc.identifier.urihttp://hdl.handle.net/11446/3548
dc.descriptionPubMed: 31926908en_US
dc.description.abstractThe brain-derived neurotrophic factor (BDNF) gene Val66Met polymorphism may cause impairment in short-term motor learning by reducing activity-dependent BDNF expression, which causes alterations in synaptic plasticity by changing glutamatergic and GABAergic synaptic transmissions. Sensory-motor integration (SMI) plays an important role in motor learning. in this study, we investigated the role of this polymorphism on SMI during a complex motor learning practice. Forty-three healthy participants performed standardized 5-day basketball shooting exercises under supervision. Electrophysiologic SMI studies were performed before the first day exercise (T0) and after the first and fifth day exercises (T1 and T2, respectively). SMI was studied using electrical median nerve stimulation at the wrist, followed by transcranial magnetic stimulation (TMS) of the contralateral motor cortex with various inter-stimulus intervals (ISIs). Recordings were made from the thenar and forearm flexor muscles. Participants were divided into two groups according to their BDNF genotype. Group 1 consisted of 26 subjects with the Val66Val genotype and group 2 included 17 subjects with the BDNF Met allele. Group 2 had a lower increase in basketball scores at day 5. Moreover, they had higher afferent facilitation for the responses recorded from both thenar and forearm flexor muscles at T1, but these changes could not be maintained until T2. This non-persistent early hyper-responsivity of the sensory-motor cortex in subjects with the BDNF Met allele might be explained by a transient upsurge of cortical excitability to compensate the insufficient cortical plasticity during motor learning, which could be considered as a sign of lower performance in motor skill learning. © 2020 Elsevier B.V.en_US
dc.description.sponsorshipIstanbul Üniversitesi: 49434en_US
dc.description.sponsorshipThis work was supported by a grant from Scientific Research Projects Coordination Unit of Istanbul University , Project Number: 49434.en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.identifier.doi10.1016/j.brainres.2020.146652en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectBDNF Met alleleen_US
dc.subjectBrain-derived neurotrophic factoren_US
dc.subjectMotor skill learningen_US
dc.subjectSensory-motor integrationen_US
dc.subjectTranscranial magnetic stimulationen_US
dc.titleEffect of the brain-derived neurotrophic factor gene Val66Met polymorphism on sensory-motor integration during a complex motor learning exerciseen_US
dc.typearticleen_US
dc.relation.journalBrain Researchen_US
dc.departmentDBÜen_US
dc.identifier.volume1732en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-tempDeveci, S.Ş., Departments of Neurology and Clinical Neurophysiology, Istanbul University, Istanbul Faculty of Medicine, Topkapı Mahallesi, Turgut Özal Millet Cd., 34093 Fatih, Istanbul, Turkey; Matur, Z., Departments of Neurology and Clinical Neurophysiology, Istanbul University, Istanbul Faculty of Medicine, Topkapı Mahallesi, Turgut Özal Millet Cd., 34093 Fatih, Istanbul, Turkey, Department of Neurology, Demiroglu (Demiroğlu) Bilim University, Medical Faculty, Esentepe Mahallesi, Büyükdere Cd. No:120, 34394 Şişli, Istanbul, Turkey; Kesim, Y.Y., Department of Genetics, Istanbul University, Aziz Sancar Institute of Experimental Medicine, Topkapı Mahallesi, Vakıf Gureba Cd., 34093 Şehremini, Fatih, Istanbul, Turkey; Senturk (Şentürk), G.G., Departments of Neurology and Clinical Neurophen_US


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