Poster Session III. - K: Theoretical and Translational Medicine
Abbas Anna
Institute of Translational Medicine
Anna Anoir Abbas1, Idris J. Jimoh2, Anikó Göblös3, Roger A. Barker4, Zoltán L. Veréb3, Johan Jakobsson5, Lajos Kemény6, Tibor Pankotai6, Judit Mária Molnár2, Karolina Pircs7
1: HCEMM, Semmelweis University
2: Semmelweis University
3: University of Szeged
4: University of Cambridge
5: Lund University
6: HCEMM, University of Szeged
7: HCEMM, Semmelweis University, Lund University
Huntington’s disease (HD) is an uncurable autosomal dominant progressive neurodegenerative disorder. The role of the dopaminergic system in developing HD symptoms is crucial, as the central dopaminergic pathways are overactivated in HD. Several drugs can reduce dopaminergic overactivity. However, their effectivity on psychiatric symptoms is limited. Moreover, the treatment of apathy and cognitive symptoms still remains challenging in HD. Cariprazine, a third-generation antipsychotic, is acting as a dopamine D3 and D2 receptor agonist. Previous results showed a positive effect in HD patients after cariprazine treatment. Clinical studies indicated positive effects in early-stage HD patients after cariprazine treatment in some psychiatric symptoms such as depressed mood, apathy and cognitive function in patients. Moreover, cariprazine also improved dopamine imbalance in the prefrontal cortex.
In this study, we investigate the effects of cariprazine using a novel in vitro model of HD, employing donor-derived aged induced neurons (iNs). Our objective is to elucidate the putative therapeutic effects of cariprazine and its mechanism of action, with a particular focus on autophagy. Using a reverse translational approach, we applied cariprazine treatment to iNs directly reprogrammed from fibroblasts of healthy controls, drug-naïve HD patients, and cariprazine-treated HD patients. High-content automated microscopy coupled with immunocytochemistry was employed for morphological and autophagy analyses. Our findings indicate that cariprazine treatment ameliorates the neurite abnormalities characteristic of HD-iNs. Furthermore, cariprazine modulated autophagic processes, suggesting a potential role in restoring subcellular autophagic dynamics. Notably, treatment with cariprazine led to a reduction in HTT gene expression. Comparative analyses with other D2/D3 antipsychotic agents suggest that these effects are attributed to the unique structural properties of cariprazine. This study provides compelling evidence supporting the therapeutic potential of cariprazine in HD.