Literature DB >> 8814237

Processing of pro-tumor necrosis factor-alpha by venom metalloproteinases: a hypothesis explaining local tissue damage following snake bite.

A M Moura-da-Silva1, G D Laing, M J Paine, J M Dennison, V Politi, J M Crampton, R D Theakston.   

Abstract

Venom-induced necrosis is a common local debilitating sequela of bites by many vipers, frequently resulting in severe permanent scarring and deformity. Antivenoms are not effective under these circumstances unless administered within a few minutes of the bite; this is unlikely to occur in the rural tropics where most victims take a long time to reach medical care. We have shown that two venom zinc metalloproteinases (jararhagin from Bothrops jararaca venom and a metalloproteinase from Echis pyramidum leakeyi venom) successfully cleaved the recombinant glutathione-S-transferase-tumor necrosis factor-alpha fusion protein (GST-TNF-alpha) substrate to form biologically active TNF-alpha which was shown to be neutralized by ovine TNF-alpha Fab antibodies. This resulted in a reduction of venom-induced necrosis in mice when injected intravenously or intradermally both before and after intradermal injections of E.p.leakeyi venom. A peptidomimetic (POL 647) was also found to inhibit the Echis metalloproteinase, thus preventing the processing of the TNF precursor; this was shown using a TNF-alpha-sensitive cell culture assay and electrophoresis. These observations demonstrate the possible importance of TNF-alpha in the development of the resulting necrotic lesion and leads to the hypothesis that increased levels of venom metalloproteinases following snake bite release active TNF-alpha. This cytokine may contribute to the local necrosis and also induce the production of endogenous matrix metalloproteinases, which in turn generate a positive feedback mechanism resulting in continued cleavage of pro-TNF-alpha. The results indicate that inhibition or neutralization of endogenous TNF-alpha appears to result in a significant reduction in venom-induced necrosis. This could help to explain the clinical observations that treatment of local necrosis following snake bite by antivenom is only minimally successful.

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Year:  1996        PMID: 8814237     DOI: 10.1002/eji.1830260905

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  20 in total

1.  Antagonization of tumor necrosis factor in snake bite. A new approach for an old threat.

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Journal:  Intensive Care Med       Date:  2001-05       Impact factor: 17.440

2.  Structures of adamalysin II with peptidic inhibitors. Implications for the design of tumor necrosis factor alpha convertase inhibitors.

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3.  Effect of purified Russell's viper venom-factor X activator (RVV-X) on renal hemodynamics, renal functions, and coagulopathy in rats.

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4.  Strong myotoxic activity of Trimeresurus malabaricus venom: role of metalloproteases.

Authors:  C D Raghavendra Gowda; R Rajesh; A Nataraju; B L Dhananjaya; A R Raghupathi; T V Gowda; B K Sharath; B S Vishwanath
Journal:  Mol Cell Biochem       Date:  2006-01       Impact factor: 3.396

5.  Importance of metalloproteinases and macrophages in viper snake envenomation-induced local inflammation.

Authors:  E P Costa; P B Clissa; C F P Teixeira; A M Moura-da-Silva
Journal:  Inflammation       Date:  2002-02       Impact factor: 4.092

6.  Unified treatment algorithm for the management of crotaline snakebite in the United States: results of an evidence-informed consensus workshop.

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7.  Antisnake Venom Activity of Hibiscus aethiopicus L. against Echis ocellatus and Naja n. nigricollis.

Authors:  S S Hasson; A A Al-Jabri; T A Sallam; M S Al-Balushi; R A A Mothana
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9.  Unusual accelerated rate of deletions and insertions in toxin genes in the venom glands of the pygmy copperhead (Austrelaps labialis) from Kangaroo island.

Authors:  Robin Doley; Nguyen Ngoc Bao Tram; Md Abu Reza; R Manjunatha Kini
Journal:  BMC Evol Biol       Date:  2008-02-28       Impact factor: 3.260

10.  Increments in cytokines and matrix metalloproteinases in skeletal muscle after injection of tissue-damaging toxins from the venom of the snake Bothrops asper.

Authors:  Alexandra Rucavado; Teresa Escalante; Catarina F P Teixeira; Cristina María Fernándes; Cecilia Diaz; José María Gutiérrez
Journal:  Mediators Inflamm       Date:  2002-04       Impact factor: 4.711

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