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The standard aqueous stem bark extract of Mangifera indica L. inhibits toxic PLA(2) – NN-XIb-PLA(2) of Indian cobra venom

The aqueous extract of Mangifera indica is known to possess diverse medicinal properties, which also includes anti-snake venom activities. However, its inhibitory potency and mechanism of action on multi-toxic snake venom phospholipases A(2)s are still unknown. Therefore, the objective of this study...

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Detalles Bibliográficos
Autores principales: Dhananjaya, Bhadrapura Lakkappa, Sudarshan, Shivalingaiah, Dongol, Yashad, More, Sunil S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4881193/
https://www.ncbi.nlm.nih.gov/pubmed/27275129
http://dx.doi.org/10.1016/j.jsps.2016.04.026
Descripción
Sumario:The aqueous extract of Mangifera indica is known to possess diverse medicinal properties, which also includes anti-snake venom activities. However, its inhibitory potency and mechanism of action on multi-toxic snake venom phospholipases A(2)s are still unknown. Therefore, the objective of this study was to evaluate the modulatory effect of standard aqueous bark extract of M. indica on NN-XIb-PLA(2) of Indian cobra venom. The in vitro sPLA(2), in situ hemolytic and in vivo edema inhibition effect were carried out as described. Also the effect of substrate and calcium concentration was carried out. M. indica extract dose dependently inhibited the GIA sPLA(2) (NN-XIb-PLA(2)) activity with an IC(50) value of 7.6 μg/ml. M. indica extract effectively inhibited the indirect hemolytic activity up to 98% at ∼40 μg/ml concentration. Further, M. indica extract (0–50 μg/ml) inhibited the edema formed in a dose dependent manner. When examined as a function of increased substrate and calcium concentration, there was no relieve of inhibitory effect of M. indica extract on the NN-XIb-PLA(2). Further, the inhibition was irreversible as evident from binding studies. The in vitro inhibition is well correlated with in situ and in vivo edema inhibiting activities of M. indica. As the inhibition is independent of substrate and calcium and was irreversible, it can be concluded that M. indica extract mode of inhibition could be due to direct interaction of components present in the extract with the PLA(2) enzyme. The aqueous extract of M. indica effectively inhibits svPLA(2) enzymatic and its associated toxic activities, which substantiate their anti-snake venom properties. Further in-depth studies on the role and mechanism of the principal constituents present in the extract, responsible for the anti-PLA(2) activity will be interesting to develop them into potent antisnake component and also as an anti-inflammatory agent.