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DOI 10.1021/acschemneuro.7b00096

Медицинская библиотека · ACS chemical neuroscience · 2017

The Marine Guanidine Alkaloid Crambescidin 816 Induces Calcium Influx and Cytotoxicity in Primary Cultures of Cortical Neurons through Glutamate Receptors.

Mendez Aida G, Juncal Andrea Boente, Silva Siguara B L, Thomas Olivier P, Martín Vázquez Víctor, Alfonso Amparo, Vieytes Mercedes R, Vale Carmen, Botana Luís M

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Crambescidin 816 is a guanidine alkaloid produced by the sponge Crambe crambe with known antitumoral activity. While the information describing the effects of this alkaloid in central neurons is scarce, Cramb816 is known to block voltage dependent calcium channels being selective for L-type channels. Moreover, Cramb816 reduced neuronal viability through an unknown mechanism. Here, we aimed to describe the toxic activity of Cramb816 in cortical neurons. Since calcium influx is considered the main mechanism responsible for neuronal cell death, the effects of Cramb816 in the cytosolic calcium concentration of cortical neurons were studied. The alkaloid decreased neuronal viability and induced a dose-dependent increase in cytosolic calcium that was also related to the presence of calcium in the extracellular media. The increase in calcium influx was age dependent, being higher in younger neurons. Moreover, this effect was prevented by glutamate receptor antagonists, which did not fully block the cytotoxic effect of Cramb816 after 24 h of treatment but completely prevented Cramb816 cytotoxicity after 10 min exposure. Therefore, the findings presented herein provide new insights into the cytotoxic effect of Cramb816 in cortical neurons.

Для цитирования: Mendez Aida G, Juncal Andrea Boente, Silva Siguara B L, Thomas Olivier P, Martín Vázquez Víctor, Alfonso Amparo, Vieytes Mercedes R, Vale Carmen, Botana Luís M. The Marine Guanidine Alkaloid Crambescidin 816 Induces Calcium Influx and Cytotoxicity in Primary Cultures of Cortical Neurons through Glutamate Receptors.. ACS chemical neuroscience. 2017. DOI: 10.1021/acschemneuro.7b00096.

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