Source:http://linkedlifedata.com/resource/pubmed/id/18996140
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2008-12-26
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pubmed:abstractText |
The ability of crude venom and a basic phospholipase A(2) (LmTX-I) from Lachesis muta muta venom to increase the microvascular permeability in rat paw and skin was investigated. Crude venom or LmTX-I were injected subplantarly or intradermally and rat paw oedema and dorsal skin plasma extravasation were measured. Histamine release from rat peritoneal mast cell was also assessed. Crude venom or LmTX-I induced dose-dependent rat paw oedema and dorsal skin plasma extravasation. Venom-induced plasma extravasation was inhibited by the histamine H(1) antagonist mepyramine (6mg/kg), histamine/5-hydroxytriptamine antagonist cyproheptadine (2mg/kg), cyclooxygenase inhibitor indomethacin (5mg/kg), nitric oxide synthesis inhibitor l-NAME (100nmol/site), tachykinin NK(1) antagonist SR140333 (1nmol/site) and bradykinin B(2) receptor antagonist Icatibant (0.6mg/kg). Platelet-activating factor (PAF) antagonist PCA4248 (5mg/kg) had no effect. LmTX-I-induced skin extravasation was inhibited by cyproheptadine, mepyramine, indomethacin and PCA4248, while l-NAME and SR140333 had no effect. Additionally, both Lachesis muta muta venom and LmTX-I concentration-dependently induced histamine release from rat mast cells. In conclusion, Lachesis muta muta venom and LmTX-I increase microvascular permeability by mechanisms involving in vivo mast cell activation and arachidonic acid metabolites. Additionally, crude venom-induced responses also involve substance P, nitric oxide and bradykinin release, whether LmTX-I-induced responses involve PAF.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Crotalid Venoms,
http://linkedlifedata.com/resource/pubmed/chemical/Lachesis venom,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide,
http://linkedlifedata.com/resource/pubmed/chemical/Prostaglandin-Endoperoxide Synthases,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Bradykinin B2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Tachykinin
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0041-0101
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
53
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
69-77
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pubmed:meshHeading |
pubmed-meshheading:18996140-Animals,
pubmed-meshheading:18996140-Cell Movement,
pubmed-meshheading:18996140-Crotalid Venoms,
pubmed-meshheading:18996140-Edema,
pubmed-meshheading:18996140-Foot,
pubmed-meshheading:18996140-Inflammation,
pubmed-meshheading:18996140-Mast Cells,
pubmed-meshheading:18996140-Nitric Oxide,
pubmed-meshheading:18996140-Prostaglandin-Endoperoxide Synthases,
pubmed-meshheading:18996140-Rats,
pubmed-meshheading:18996140-Receptor, Bradykinin B2,
pubmed-meshheading:18996140-Receptors, Tachykinin,
pubmed-meshheading:18996140-Skin,
pubmed-meshheading:18996140-Viperidae
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pubmed:year |
2009
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pubmed:articleTitle |
Inflammatory oedema induced by Lachesis muta muta (Surucucu) venom and LmTX-I in the rat paw and dorsal skin.
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pubmed:affiliation |
Department of Pharmacology, Faculty of Medical Sciences (FCM), UNICAMP, PO Box 6111, 13084-971 Campinas, SP, Brazil.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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