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Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.

We have provided evidence that: (a) lethality of mice to crude Bothrops venom varies according the isogenic strain (A/J > C57Bl/6 > A/Sn > BALB/c > C3H/HePas > DBA/2 > C3H/He); (b)BALB/c mice (LD50=100.0 microg) were injected i.p. with 50 microg of venom produced IL-6, IL-10, INF-g...

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Autores principales: Barros, S F, Friedlanskaia, I, Petricevich, V L, Kipnis, T L
Formato: Texto
Lenguaje:English
Publicado: 1998
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781860/
https://www.ncbi.nlm.nih.gov/pubmed/9883969
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author Barros, S F
Friedlanskaia, I
Petricevich, V L
Kipnis, T L
author_facet Barros, S F
Friedlanskaia, I
Petricevich, V L
Kipnis, T L
author_sort Barros, S F
collection PubMed
description We have provided evidence that: (a) lethality of mice to crude Bothrops venom varies according the isogenic strain (A/J > C57Bl/6 > A/Sn > BALB/c > C3H/HePas > DBA/2 > C3H/He); (b)BALB/c mice (LD50=100.0 microg) were injected i.p. with 50 microg of venom produced IL-6, IL-10, INF-gamma, TNF-alpha and NO in the serum. In vitro the cells from the mice injected and challenged with the venom only released IL-10 while peritoneal macrophages released IL-10, INF-gamma and less amounts of IL-6; (c) establishment of local inflammation and necrosis induced by the venom, coincides with the peaks of TNF-alpha, IFN-gamma and NO and the damage was neutralized when the venom was incubated with a monoclonal antibody against a 60 kDa haemorrhagic factor. These results suggest that susceptibility to Bothrops atrox venom is genetically dependent but MHC independent; that IL-6, IL-10, TNF-alpha, IFN-gamma and NO can be involved in the mediation of tissue damage; and that the major venom component inducers of the lesions are haemorrhagins.
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spelling pubmed-17818602007-01-25 Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom. Barros, S F Friedlanskaia, I Petricevich, V L Kipnis, T L Mediators Inflamm Research Article We have provided evidence that: (a) lethality of mice to crude Bothrops venom varies according the isogenic strain (A/J > C57Bl/6 > A/Sn > BALB/c > C3H/HePas > DBA/2 > C3H/He); (b)BALB/c mice (LD50=100.0 microg) were injected i.p. with 50 microg of venom produced IL-6, IL-10, INF-gamma, TNF-alpha and NO in the serum. In vitro the cells from the mice injected and challenged with the venom only released IL-10 while peritoneal macrophages released IL-10, INF-gamma and less amounts of IL-6; (c) establishment of local inflammation and necrosis induced by the venom, coincides with the peaks of TNF-alpha, IFN-gamma and NO and the damage was neutralized when the venom was incubated with a monoclonal antibody against a 60 kDa haemorrhagic factor. These results suggest that susceptibility to Bothrops atrox venom is genetically dependent but MHC independent; that IL-6, IL-10, TNF-alpha, IFN-gamma and NO can be involved in the mediation of tissue damage; and that the major venom component inducers of the lesions are haemorrhagins. 1998 /pmc/articles/PMC1781860/ /pubmed/9883969 Text en
spellingShingle Research Article
Barros, S F
Friedlanskaia, I
Petricevich, V L
Kipnis, T L
Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title_full Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title_fullStr Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title_full_unstemmed Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title_short Local inflammation, lethality and cytokine release in mice injected with Bothrops atrox venom.
title_sort local inflammation, lethality and cytokine release in mice injected with bothrops atrox venom.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1781860/
https://www.ncbi.nlm.nih.gov/pubmed/9883969
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