COGNITIVE AND MOTOR DYSFUNCTION IN zQ175 HUNTINGTON´S DISEASE MICE

BRUNO, JULIETA; LÓPEZ COUSELO FEDERICO; RIVAS DIEGO; PALMIERI MATEO; SABA JULIETA; CARNIGLIA LILA; DURAND DANIELA; LASAGA MERCEDES; CARUSO CARLA

Mar del Plata

Congreso; REUNIÓN CONJUNTA SAIC SAI&FAIC SAFIS 2022; 2022

SAIC

Huntington’s Disease is a neurodegenerative genetic disorder caused by CAG repeat expansion in the huntingtin gene that generates motor, cognitive and psyquiatric symptoms in humans. In thiswork, our objective was to evaluate sex differences in cognitive and motor function of zQ175 knock-in (HD) and wild type (WT) mice at 4 or 8 months (M) of age. We tested their behavior by using the open field test, the gait analysis, and the novel object recognition (NOR) test. Results: In the open field test, HD female mice traveled less distance, moved more slowly (p