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J Venom Res
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03-04 April 2019, Oxford
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Heparin at low concentration acts as antivenom against Bothrops jararacussu venom and bothropstoxin-I neurotoxic and myotoxic actions

Research Report 


J Venom Res 
(2010), Vol 1, 54-60

doi:

Published online: 15 October 2010

Full Text: (html | XML | pdf 226kb)

Heparin at low concentration acts as antivenom against Bothrops jararacussu venom and bothropstoxin-I neurotoxic and myotoxic actions

Sandro Rostelato-Ferreira †, Gildo Bernardo Leite †, Adélia Cristina Oliveira Cintra ‡, Maria Alice da Cruz-Höfl ing §, Léa Rodrigues-Simioni †, Yoko Oshima-Franco †δ*

† Departamento de Farmacologia, Faculdade de Ciências Médicas, CP 6111, Universidade Estadual de Campinas – UNICAMP, Brasil

‡ Departamento de Análises Clínicas, Toxicológica e Bromatológica, Faculdade de Ciências Farmacêuticas, Universidade de São Paulo, Ribeirão Preto, SP, Brasil

§ Departamento de Histologia e Embriologia, Instituto de Biologia, C.P. 6109, Universidade Estadual de Campinas – UNICAMP, CEP 13083-970 Campinas, SP, Brasil

δ Curso de Farmácia, Universidade de Sorocaba, Sorocaba, SP, Brasil

*Correspondence to: Yoko Oshima-Franco, Email: yofranco@terra.com.br, Tel: +55 019 3521 9533, Fax: +55 019 3289 2968

Received: 03 September 2010, Accepted: 27 September 2010

© Copyright The Authors

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ABSTRACT

IHeparin has been shown to antagonize myotoxic effects of crotaline venoms. Here a very low heparin concentration (LHC) was examined in its ability to antagonize the neurotoxic/myotoxic effects of Bothrops jararacussu venom and its phospholipase A2 myotoxin, bothropstoxin-I (BthTX-I), in an in vitro nervemuscle preparation and in mice gastrocnemius. Normalization of results was done by assays with commercial antibothropic antivenom (CBA). LHC (1 IU/ml) added to the incubation bath reduced by 4- and 4.5-fold (vs 2.8- and 2.5-fold by CBA) the neuromuscular paralysis, by 5.4 and 4.4-fold (vs 2.5- and 13.3-fold by CBA) the percentage of fi bers damaged and by 6- and 1.7-fold (vs 30- and 1.6-fold by CBA) the CK activity induced by B. jararacussu and BthTX-I, respectively. Protamine sulphate added 15min after the incubation of the preparation
with LHC+venom, avoided the LHC neutralizing effect against venom neurotoxicity. This strongly attests that given the polycationic nature of protamine, it probably complexed with the polyanionic heparin making it unattainable for binding to basic components of venom, reducing toxicity. Since heparin antagonism is generally stronger against venom effects than is myotoxin we discuss that other venom components than the BthTX-I are likely target for the antagonism promoted by the polyanionic heparin.

KEYWORDS: Antagonism , neuromuscular junction , neutralization , protamine

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