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Neurosci Lett ; 835: 137843, 2024 Jul 13.
Article in English | MEDLINE | ID: mdl-38821201

ABSTRACT

Neuropsychological studies report anxiety and depression like symptoms in patients suffering from lifestyle disorder but its impact on locomotor function lacks clarity. Our study investigates locomotor deficits resulting due to perturbations in cerebellum of high fat diet (HFD), chronodisruption (CD) or a combination (HCD) model of lifestyle disorder. Significant downregulation in levels of cerebellar clock genes (Bmal-1, Clock, Per 1 and Per 2) and Bdnf-Trkb pathway genes (Bdnf, TrkB and Syn1 levels) were recorded. Further, locomotor deficits were observed in all the three experimental groups as evidenced by actimeter test, pole test and wire hanging test. Nuclear pyknosis of Purkinje cells, their derangement and inflammation were the hallmark of cerebellar tissue of all the three experimental groups. Taken together, this study generates important links between cerebellar clock oscillations, locomotor function and Bdnf-TrkB signaling.


Subject(s)
Brain-Derived Neurotrophic Factor , Cerebellum , Receptor, trkB , Signal Transduction , Brain-Derived Neurotrophic Factor/metabolism , Brain-Derived Neurotrophic Factor/genetics , Animals , Receptor, trkB/metabolism , Receptor, trkB/genetics , Cerebellum/metabolism , Male , Diet, High-Fat/adverse effects , Locomotion/physiology , Purkinje Cells/metabolism
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