| Literature DB >> 34962383 |
Marta Vela1, María Adelaida García-Gimeno2, Ana Sanchis3,4, José Bono-Yagüe3,4, José Cumella1, Laura Lagartera1, Concepción Pérez1, Eva-María Priego1, Angela Campos5,6, Pascual Sanz5,6, Rafael P Vázquez-Manrique3,4,5, Ana Castro1.
Abstract
Aggregation of mutant huntingtin, because of an expanded polyglutamine track, underlies the cause of neurodegeneration in Huntington disease (HD). However, it remains unclear how some alterations at the cellular level lead to specific structural changes in HD brains. In this context, the neuroprotective effect of the activation of AMP-activated protein kinase (AMPK) appears to be a determinant factor in several neurodegenerative diseases, including HD. In the present work, we describe a series of indole-derived compounds able to activate AMPK at the cellular level. By using animal models of HD (both worms and mice), we demonstrate the in vivo efficacy of one of these compounds (IND1316), confirming that it can reduce the neuropathological symptoms of this disease. Taken together, in vivo results and in silico studies of druggability, allow us to suggest that IND1316 could be considered as a promising new lead compound for the treatment of HD and other central nervous system diseases in which the activation of AMPK results in neuroprotection.Entities:
Keywords: ADME in silico; AMPK; C. elegans models; Huntington disease mouse models; indole derivatives; neuroprotection; polyQ toxicity
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Year: 2021 PMID: 34962383 PMCID: PMC8822144 DOI: 10.1021/acschemneuro.1c00758
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418