D-013
YERBA MATE AND CGA ACTIVATE AMPK, PROMOTE AUTOPHAGY AND DECREASE A-SYN AGREGATION IN CELL CULTURE.
Hernán Ezequiel Hauché Pedernera1, Malena Russo1, Paula López Martin1, Melina Bordone1, Tiago Outeiro2, Juan Ferrario1
  1. Laboratorio de Neurobiología de la Enfermedad de Parkinson ,Instituto de Biociencias, Biomedicina y Biología traslacional (IB3, UBA) Ciudad Autónoma de Buenos Aires, Argentina.
  2. Department of Experimental Neurodegeneration, Center for Biostructural Imaging of Neurodegeneration, University Medical Center Goettingen, Goettingen, Germany; Max Planck Institute for Experimental Medicine, Goettingen, Germany; Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Framlington Place, Newcastle Upon Tyne NE2 4HH, UK.
Presenting Author:
Hernán Ezequiel Hauché Pedernera
hernanhauche@gmail.com
Neuroprotection is a key goal in the study of neurodegenerative diseases such as Parkinson’s disease (PD), where progressive dopaminergic neuron loss causes severe motor and cognitive deficits. Epidemiological studies suggest that consumption of Yerba Mate (Ilex paraguariensis, YM), as well as coffee and green tea, is associated with reduced PD risk. These beverages contain polyphenols, particularly chlorogenic acid (CGA), proposed to mediate neuroprotective effects. We previously showed that YM protects dopaminergic neurons in primary cultures, but the underlying mechanisms remain unclear, especially those involving neuronal survival and protein homeostasis. Here, we investigated whether YM and CGA modulate pathways relevant to neuroprotection, focusing on AMPK activation, autophagy, and α-synuclein (α-Syn) aggregation. SH-SY5Y cells were used to evaluate AMPK phosphorylation after treatment with YM or CGA, while autophagy was assessed by LC3 ICC. In parallel, α-Syn aggregation was analyzed in H4 cells co-transfected with SynT and Synphilin-1. YM and CGA increased AMPK phosphorylation, suggesting activation of survival pathways. ICC revealed more LC3-positive puncta, indicating autophagy induction. In H4 cells, YM and CGA reduced the number and size of α-Syn aggregates. Altogether, these findings support that YM and CGA stimulate AMPK signaling, promote autophagy, and attenuate protein aggregation, highlighting YM as a promising dietary candidate for further studies in PD.