IBIOBA - MPSP   22718
INSTITUTO DE INVESTIGACION EN BIOMEDICINA DE BUENOS AIRES - INSTITUTO PARTNER DE LA SOCIEDAD MAX PLANCK
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Neuroprotective effect of Yerba mate (Ilex paraguariensis) on cultured dopaminergic neurons, from in vitro to Drosophila models of Parkinson?s disease
Autor/es:
MARIANA FERRARIO; OSCAR GERSHANIK; JUAN FERRARIO; PEDRO BALLESTERO; MARCELA SCHENK; ALEJANDRA BERNARDI; SANDRA GUERRERO; IRENE TARAVINI; NARA I. MURARO
Lugar:
Ciudad de Córdoba
Reunión:
Congreso; XXXIII Congreso Anual de la Sociedad Argentina de Investigación en Neurociencias; 2018
Institución organizadora:
Sociedad Argentina de Investigación en Neurociencias
Resumen:
Parkinson's disease (PD) is the second worldwide neurodegenerative disorder in prevalence. Its origin is unknown, but its pathophysiological characteristic is the progressive degeneration of dopamine-releasing neurons (nDA) of the Substantia nigra pars compacta. Recently, a study conducted in Argentina revealed that the consumption of yerba mate (YM) has an inverse association with the risk of developing PD. With the aim of demonstrating the putative neuroprotective properties of YM on nDA, we are undertaking experimental approaches both in vitro and in vivo. First, we studied the survival of mouse nDA on primary cultures treated with YM extract, and found that YM provides higher neuroprotection over nDA than other known agents, such as caffeine. To delve into the basis of this neuroprotection, we have also tested some of the major compounds of the YM extract, such as chlorogenic acid and theobromine.Given these promising results, we hypothesized that the YM extract could also protect nDA in vivo from the degeneration caused by the expression of a-syn in a Drosophila melanogaster model of PD, and improve the related locomotor deficit. To reach this goal, we have set up the administration of YM to these flies and produced preliminary behavioral and histological data. Our results demonstrate that YM protects nDA in vitro and set the grounds to study such effect on a simply, but very powerful, in vivo model of PD.