EVALUATION OF ANTIVENOM ACTIVITY OF CALOTROPIS GIGANTEA PLANT EXTRACT AGAINST VIPERA RUSSELLI SNAKE VENOM
AbstractEthnopharmacological relevance: Calotropis gigantea is usedtraditionally to treat common diseases such as fever, rheumatism, indigestion, cough, cold, eczema, asthma, elephantiasis, nausea, vomiting and diarrhoea, either alone or with other medicines
Aim of the study: To evaluate the antivenom activity of Calotropis gigantea plantextract against Vipera russelli snake venom
Materials and methods: The lyophilized snake venom of Vipera Russelli was dissolved in saline and required concentrations were prepared. Lyophilized polyvalent snake venom antiserum was used as reference serum. The methanolic extract of Calotropis gigantea was evaluated for its efficacy to neutralize various actions of the venom like lethality, necrotizing activity, edema forming activity and haemorrahgic activity.
Results: Oral administration of C. gigantea plant extract at dose levels 200 and 400 mg/kg body weight effectively neutralized the lethal effect of 2LD50 and 3LD50 of V. russelli venom in mice (in-vivo neutralization). In in-vitro studies, the plant extract at all dose levels, i.e. 100, 200 and 400mg/kg body weight effectively neutralized 2LD50 and 3 LD50 of Vipera russelli venom. Oral administration of the plant extract at various dose levels was found to effectively inhibit the induction of haemorrhage and necrosis by the venom. At doses 200 and 400 mg/kg, the antinecrotic effect of plant extract was significant. The effect of methanolic extract of C. gigantea against edema induced by viperid venom was studied at 60, 120, 180 and 240 minutes. Plant extract at dose levels 200mg/kg and 400mg/kg showed significant anti-inflammatory activity at 240 min, and effect was comparable with that produced by the antivenom.
Conclusion: Present study confirms the anti snake venom activity of alcoholic extract of C. gigantea.
Article Information
57
2272-2279
676KB
1915
English
IJPSR
Nimmy Chacko*, Mohammed Ibrahim , Prerana Shetty and C.S. Shastry
Department of Pharmacology, Department of Pharmaceutical Chemistry, NGSM Institute of Pharmaceutical Sciences, Paneer, Deralakatte, Manglore, Karnataka, India
27 March, 2012
18 May, 2012
22 June, 2012
http://dx.doi.org/10.13040/IJPSR.0975-8232.3(7).2272-79
01 July, 2012