Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 1998;7(5):339-46.
doi: 10.1080/09629359890866.

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

Affiliations
Comparative Study

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

S F Barros et al. Mediators Inflamm. 1998.

Abstract

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.

PubMed Disclaimer

Similar articles

Cited by

References

    1. J Exp Med. 1967 Dec 1;126(6):1027-48 - PubMed
    1. Immunol Today. 1997 May;18(5):231-40 - PubMed
    1. Rev Inst Med Trop Sao Paulo. 1986 Jul-Aug;28(4):220-7 - PubMed
    1. J Immunol. 1988 Sep 1;141(5):1576-81 - PubMed
    1. Science. 1989 Mar 17;243(4897):1464-6 - PubMed

Publication types

MeSH terms