IFEC   20925
INSTITUTO DE FARMACOLOGIA EXPERIMENTAL DE CORDOBA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Cellular Dysfunction in a Neurotoxic Model of Parkinson´s Disease: Implications in Memory and Motor Systems
Autor/es:
MACARENA LORENA HERRERA; VICTORIA B OCCHIEPPO; ROMINA DEZA-PONZIO; VICTOR A MOLINA; NATALIA A. MARCHESE; MARÍA JOSÉ BELLINI; OSVALDO M. BASMADJIAN; MIRIAM B. VIRGOLINI; CLAUDIA B. HEREÑÚ
Lugar:
Bilbao
Reunión:
Congreso; 47th Eurpoean Brain & Behaviour Society Meeting 2017. Septiembre 2017.; 2017
Resumen:
BACKGROUND: Parkinson?s disease (PD) is the second most common neurodegenerative disorder and is characterized pathologically by the loss of dopaminergic neurons in the substantia nigra. Although motor symptoms are the main clinical features of PD, increasing evidence has shown that PD patients also have non-motor symptoms, where cognitive dysfunction is one of the most common and devastating in this neuropathology. These non-motor symptoms result from the dysfunction of interconnected systems, including the striatum, the neocortex and the hippocampus. Among the different hypothesis related to PD etiology, it is known an abnormal aldehyde dehydrogenase 2 (ALDH2) functionality in neurotransmitter degradation. This leads to the accumulation of neurotoxic metabolites, which have been associated with neuronal cell death andneurodegeneration.OBJECTIVES: 1) determine working memory and spatial memory deficits and its correlation with motor function; 2) correlate these behavioral changes with the loss of dopaminergic neurons; 3)evaluate ALDH2 expression in a 6OHDA animal model; 4) identify neuronal apoptosis in thismodelMETHODS: Male Wistar rats were bilaterally injected in dorsal striatum (CPu) with either the neurotoxic (6OHDA rats) or vehicle (SHAM rats). Twenty days after the lesion the animals were tested for working memory with the Y-maze test and short-term spatial memory with a modified version of Y-maze test. Motor function was characterized using locomotor activity with amphetamine Administration, stick and hot plate tests. At the end of the study the rats wereperfused, their brains fixed and immunohistochemistry performed for TH and ALDH2 in CPu, substantia nigra (SN), dorsal hippocampus (CA1) and prefrontal cortex (PFC) and we identifyapoptotic bodies stained with cresyl violet. All data were compared by Student´s t-test and 2-way ANOVA (p