ePoster · Neuroscience
Anika Frank, Se Joon Choi, Siham Bouhmahouad, Jonas Bendig, David Sulzer · FENS Forum 2024
Electroconvulsive therapy (ECT) is a well-established treatment for psychiatric disorders. Recent reports show that ECT improves motor deficits in Parkinson's disease (PD), while the mechanism of action remains unclear. To investigate the effects of ECT in PD, we produced partial dopaminergic depletion by unilateral striatal injection of 6-OHDA. After three weeks, behavioral testing was performed using the open field and corridor test. Animals with a lateralized phenotype were randomized into ECT or sham treatment. After a two-week treatment interval with daily ECT, behavioral testing was repe
ePoster · Neuroscience
Alina-Mariuca Marinescu, Eshita Kamal, Peter Leary, Natasa Savic, Marie A. Labouesse · FENS Forum 2024
Abnormal reward and threat processing are key players in psychiatric conditions such as eating disorders, addiction or depression. These functions are strongly regulated by the nucleus accumbens shell (NAcSh) which integrates emotional signals to regulate motor output. Historically the NAcSh was thought to consist of 2 pathways: dopamine 1 and 2 receptor-expressing striatal projection neurons (D1, D2-SPNs) which promoted reward and aversive behavior, respectively. Yet recent work has revealed that both cell types can promote either reward or aversion, depending on the NAcSh subregion or input/
ePoster · Neuroscience
Pilar Martínez Olondo, Patricia Bonnavion, Christophe Varin, Ghazal Fakhfouri, Aurélie de Groote, Amandine Cornil, Ramiro Lorenzo López, Elsa Isingrini, Elisa Pozuelo, Kathleen Xu, Eleni Tzavara, Erika Vigneault, Sylvie Dumas, Alban de Kerchove d'Exaerde, Bruno Giros · FENS Forum 2024
The prevailing model of the basal ganglia motor control posits that the striatum, the input nucleus fo the basal ganglia, orchestrates the selection of voluntary actions through two circuits, the direct and the indirect pathways that oppose each other in thalamocortical activation. These circuits originate from two different populations of spiny projecting neurons (SPNs) projecting to different output structures and classically distinguished by differential expression of dopamine (DA) D1 receptor- and D2 receptor (D1-SPNs and D2-SPNs), respectively, regardless of SPNs co-expressing these two r