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Journal Article

Citation

Oliveira RS, Leal AP, Ogata B, Moreira de Almeida CG, dos Santos DS, Lorentz LH, Moreira CM, de Castro Figueiredo Bordon K, Arantes EC, dos Santos TG, Dal Belo CA, Vinadé L. Neurotoxicology 2018; 65: 264-271.

Affiliation

Laboratório de Neurobiologia e Toxinologia, LANETOX, Universidade Federal do Pampa (UNIPAMPA), Av. Antônio Trilha 1847, 97300-000, São Gabriel, RS, Brazil.

Copyright

(Copyright © 2018, Elsevier Publishing)

DOI

10.1016/j.neuro.2017.11.006

PMID

29174112

Abstract

The biological activity of Rhinella icterica toxic secretion (RITS) was evaluated on chick neuromuscular junctions, rat heart́s tissue and mice hippocampal slices. At chick biventer cervicis preparation, RITS (5, 10 and 20μg/mL) produced a concentration-independent irreversible neuromuscular blockade, which was preceded by a transitory increase of muscle twitch tension with the lowest concentration, in 120minutes recordings. In this set of experiments, RITS incubation partially prevented the curare neuromuscular blockade. The assessment of chick biventer cervicis muscle acetylcholinesterase (AChE) in the presence of RITS showed a significant inhibition of the enzyme, similarly to neostigmine. The incubation of muscles with digoxin or ouabain mimicked the poison activity by increasing the amplitude of the twitches followed by a progressive depression of the muscle strength. In addition, RITS demonstrated a digitalic-like activity, by inhibiting significantly the cardiac Na+, K+-ATPase. When the central nervous system was accessed, RITS induced an increase in the cell viability, in the lowest concentration. In addition, the poison protected slices subject to oxygen/glucose deprivation. Altogether, these data indicate that the poisonous extract of R. icterica is able to interfere with peripheral and central neurotransmission, probably due to a direct interaction with AChE, calcium channels and Na+, K+-ATPase. A further investigation upon the poison toxic components will unveil the components involved in such a pharmacological activity and the potential biotechnological application of this poison.

Copyright © 2017 Elsevier B.V. All rights reserved.


Language: en

Keywords

Toad poison; neuromuscular blockade; neuroprotection; vertebrates

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