Publicación:
Biochemical and Behavioral Characterization of IN14, a New Inhibitor of HDACs with Antidepressant-Like Properties

Unidades académicas

Unidad Académica
Instituto de Química Aplicada
Este instituto atiende a las necesidades de aplicación del conocimiento tanto en el área química como en los temas multidisciplinarios

Grado Académico

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Resumen

Evidence suggests that histone deacetylases (HDACs) inhibitors could be used as an effective treatment for some psychiatric and neurological conditions such as depression, anxiety and age-related cognitive decline. However, non-specific HDAC inhibiting compounds have a clear disadvantage regarding their efficacy and safety, thus the need to develop more selective ones. The present study evaluated the toxicity, the capacity to inhibit HDAC activity and antidepressant-like activity of three recently described class I HDAC inhibitors IN01, IN04 and IN14, using A. salina toxicity test, in vitro fluorometric HDAC activity assay and forced-swimming test, respectively. Our data show that IN14 possesses a better profile than the other two. Therefore, the pro-cognitive and antidepressant effects of IN14 were evaluated. In the forced-swimming test model of depression, intraperitoneal administration of IN14 (100 mg/Kg/day) for five days decreased immobility, a putative marker of behavioral despair, significantly more than tricyclic antidepressant desipramine, while also increasing climbing behavior, a putative marker of motivational behavior. On the other hand, IN14 left the retention latency in the elevated T-maze unaltered. These results suggest that novel HDAC class I inhibitor IN14 may represent a promising new antidepressant with low toxicity and encourages further studies on this compound.

Descripción

Citación

Martínez-Pacheco, H., Picazo, O., López-Torres, A., Morin, J.-P., Castro-Cerritos, K. V., Zepeda, R. C., & Roldán-Roldán, G. (2020). Biochemical and behavioral characterization of IN14, a new inhibitor of HDACs with antidepressant-like properties. Biomolecules, 10(2), 299. https://doi.org/10.3390/biom10020299

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