Artículo

An alkaloid extract obtained from Phlegmariurus Saururus induces neuroprotection after status epilepticus

Danelon, Víctor Icon; Montroull, Laura Ester Icon; Vallejo, Mariana Guadalupe Icon; Cabrera, Jose Luis Icon; Agnese, Alicia Mariel ; Ortega, María Gabriela Icon; Masco, Daniel Hugo Icon

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Fecha

10/2017

Editorial

Elsevier Gmbh

Revista

Phytomedicine

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Institución organizadora

ISSN

0944-7113

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Inglés

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Resumen

Background The brain is exposed to many excitotoxic insults that can lead to neuronal damage. Among these, Epilepsy is a neurological disease that affects a large percentage of world population and is commonly associated with cognitive disorders and excitotoxic neuronal death. Most experimental strategies are focused on preventing Status Epilepticus (SE), but once it has already occurred, the key question is whether it is possible to save neurons. Purpose The aim of this study was to determine if a purified alkaloid extract (AE) obtained from Phlegmariurus saururus, a genus of Lycophyte plants (sometimes known as firmossesor fir club mosses) could induce neuroprotection following SE. Methods In vitro and in vivo techniques were applied for this purpose. Protein levels were measured by western blotting procedures. Neuronal death analysis was performed by calcein-ethidium staining and the presence of the NeuN protein as a marker for presence or absence of cells (in vitro experiments) and by Fluoro Jade B staining for the in vivo experiments. Results The effect of AE in the hippocampal neurons culture was the first determination, where we found an increase in neuronal survival and in the level of pErk and TrkB activation, 24 h after the addition of AE. In a well-established in vitro model of SE, we found that 24 h after being added to the hippocampal neuron-astrocyte co-culture, the AE induces a significant increase in neuronal survival. In addition to this, in the in vivo Li-pilocarpine model of SE, the AE induced a remarkable neuroprotection in areas such as the entorhinal cortex and hippocampal CA1 area. Conclusion These results make the AE an excellent candidate for potential clinical use in neurological disorders where memory impairment and neuronal death occurs.

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