2012
DOI: 10.1016/j.toxicon.2012.03.004
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Local inflammatory events induced by Bothrops atrox snake venom and the release of distinct classes of inflammatory mediators

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Cited by 78 publications
(58 citation statements)
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“…These venom components can be classified into procoagulants, anticoagulants, fibrinolytic toxins, vessel wall interactive toxins, toxins that affect platelet activity and plasma protein activators . These not only destroy tissues, but can also evoke a significant inflammatory response through cytokine release in the victim . In viperine (adders) and crotaline (rattlesnakes) species, inflammation is a major characteristic of envenoming and inflammation and coagulation are known to inadvertently activate each other …”
Section: Introductionmentioning
confidence: 99%
“…These venom components can be classified into procoagulants, anticoagulants, fibrinolytic toxins, vessel wall interactive toxins, toxins that affect platelet activity and plasma protein activators . These not only destroy tissues, but can also evoke a significant inflammatory response through cytokine release in the victim . In viperine (adders) and crotaline (rattlesnakes) species, inflammation is a major characteristic of envenoming and inflammation and coagulation are known to inadvertently activate each other …”
Section: Introductionmentioning
confidence: 99%
“…In addition, venom has been shown to have pro- and anti-inflammatory properties and has been shown to regulate the expression of inflammatory mediators such as IL-1β, IL-6, IL-10, IL-22, TNF-α, PGD2, PGE2, and TXA2 [18,19,21,41,42,43,44]. In this study, we constructed and screened an H. cyanocinctus venom gland T7 phage display library and discovered H-TL1, a natural peptide with antagonizing effects against TNF-α.…”
Section: Discussionmentioning
confidence: 99%
“…Bothrops atrox venom, for example, was shown to increase the vascular permeability in mice, inducing leukocyte influx between 1 and 8 h after i.p. injection and releasing important inflammatory mediators such as the eicosanoids PGD 2 , PGE 2 , TXA 2 , LTB 4 , the cytokines TNF-α, IL-6, IL-10, and the chemokine CCL-2 [52]. These inflammatory effects are most commonly related to phospholipases A 2 and metalloproteinases [72,73], although other classes of enzymes may also contribute to these responses [49].…”
Section: Discussionmentioning
confidence: 99%