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Role of crotoxin in coagulation: novel insights into anticoagulant mechanisms and impairment of inflammation-induced coagulation

BACKGROUND: Snake venom phospholipases A(2) (svPLA(2)) are biologically active toxins, capable of triggering and modulating a wide range of biological functions. Among the svPLA(2)s, crotoxin (CTX) has been in the spotlight of bioprospecting research due to its role in modulating immune response and...

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Detalles Bibliográficos
Autores principales: Gimenez, Bruna Terada, Cezarette, Gabriel Neves, Bomfim, Aline de Sousa, Monteiro, Wuelton Marcelo, Russo, Elisa Maria de Sousa, Frantz, Fabiani Gai, Sampaio, Suely Vilela, Sartim, Marco Aurelio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centro de Estudos de Venenos e Animais Peçonhentos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7702976/
https://www.ncbi.nlm.nih.gov/pubmed/33293940
http://dx.doi.org/10.1590/1678-9199-JVATITD-2020-0076
Descripción
Sumario:BACKGROUND: Snake venom phospholipases A(2) (svPLA(2)) are biologically active toxins, capable of triggering and modulating a wide range of biological functions. Among the svPLA(2)s, crotoxin (CTX) has been in the spotlight of bioprospecting research due to its role in modulating immune response and hemostasis. In the present study, novel anticoagulant mechanisms of CTX, and the modulation of inflammation-induced coagulation were investigated. METHODS: CTX anticoagulant activity was evaluated using platelet poor plasma (PPP) and whole blood (WB), and also using isolated coagulation factors and complexes. The toxin modulation of procoagulant and pro-inflammatory effects was evaluated using the expression of tissue factor (TF) and cytokines in lipopolysaccharide (LPS)-treated peripheral blood mononuclear cells (PBMC) and in WB. RESULTS: The results showed that CTX impaired clot formation in both PPP and WB, and was responsible for the inhibition of both intrinsic (TF/factor VIIa) and extrinsic (factor IXa/factor VIIIa) tenase complexes, but not for factor Xa and thrombin alone. In addition, the PLA(2) mitigated the prothrombinase complex by modulating the coagulation phospholipid role in the complex. In regards to the inflammation-coagulation cross talk, the toxin was capable of reducing the production of the pro-inflammatory cytokines IL-1β, IL-6 and TNF-α, and was followed by decreased levels of TF and procoagulant activity from LPS-treated PBMC either isolated or in WB. CONCLUSION: The results obtained in the present study recognize the toxin as a novel medicinal candidate to be applied in inflammatory diseases with coagulation disorders.