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Neuroprotective properties of RT10, a fraction isolated from Parawixia bistriata spider venom, against excitotoxicity injury in neuron-glia cultures
Journal article   Open access   Peer reviewed

Neuroprotective properties of RT10, a fraction isolated from Parawixia bistriata spider venom, against excitotoxicity injury in neuron-glia cultures

Eduardo Octaviano Primini, José Luiz Liberato, Andreia Cristina Karklin Fontana and Wagner Ferreira Dos Santos
The journal of venomous animals and toxins including tropical diseases, v 25, pp e148818-e148818
2019
PMID: 31131008
url
http://www.scielo.br/pdf/jvatitd/v25/1678-9199-jvatitd-25-e148818.pdfView
Published, Version of Record (VoR) Open
url
https://doi.org/10.1590/1678-9199-JVATITD-1488-18View
Published, Version of Record (VoR) Open

Abstract

Parawixia bistriata excitotoxicity L-Glutamate neuroprotection RT10
Glutamate ( Glu), the major excitatory neurotransmitter in the mammalian Central Nervous System (CNS), is essential to cognitive functions. However, when Glu is accumulated in large concentrations at the synaptic cleft, it can induce excitotoxicity that results in secondary damage implicated in many neurological disorders. Current therapies for the treatment of neurological disorders are ineffective and have side effects associated with their use; therefore, there is a need to develop novel treatments. In this regard, previous studies have shown that neuroactive compounds obtained from the venom of the spider have neuroprotective effects and In this sense, this work aimed to evaluate potential neuroprotective effects of fraction RT10, obtained from this spider venom, on primary cultures of neuron and glial cells subjected to glutamate excitotoxicity insults. Primary cultures of neurons and glia were obtained from the cerebral tissue of 1-day-old postnatal Wistar rats. After 7 days (DIV), the cultures were incubated with fraction RT10 (0.002; 0.02; 0.2 and 2 µg/µL) or riluzole (100 µM) for 3-hours before application of 5 mM Glu. After 12 hours, the resazurin sodium salt (RSS) test was applied to measure metabolic activity and proliferation of living cells, whereas immunocytochemistry for MAP2 was performed to measure neuronal survival. In addition, the cells were immunolabeled with NeuN and GFAP in baseline conditions. In the RSS tests, we observed that pre-incubation with RT10 before the excitotoxic insults from -Glu resulted in neuroprotection, shown by a 10% reduction in the cell death level. RT10 was more effective than riluzole, which resulted in a cell-death reduction of 5%. Moreover, qualitative analysis of neuronal morphology (by MAP2 staining, expressed as fluorescence intensity (FI), an indirect measure of neuronal survival) indicate that RT10 reduced the toxic effects of -Glu, as shown by a 38 % increase in MAP2 fluorescence when compared to -Glu insult. On the other hand, the riluzole treatment resulted in 17% increase of MAP2 fluorescence; therefore, the neuroprotection from RT10 was more efficacious. RT10 fraction exhibits neuroprotective effects against -Glu excitotoxicity in neuron-glia cultured .

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Collaboration types
Domestic collaboration
International collaboration
Web of Science research areas
Toxicology
Tropical Medicine
Zoology
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