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Efficacy Testing of Commercially Available Anti-snake Venoms against Echis ocellatus Venom in Northern Nigeria


Yusuf Abubakar Muhammad
Auwal Adam Bala
Shehu Yakubu Magaji
Abdullahi Ibrahim Doma
Abdullahi Rabiu Abubakar
Suleiman Yunusa Goji
Zainab Gambo Ibrahim
Ibrahim Muhammad
Sani Malami
Basheer Z.A Chedi

Abstract

Snakebites cause considerable morbidity and mortality worldwide, with the highest burden found in Sub-Saharan Africa and South Asia. The aim of this  study was to evaluate the efficacy of Echitab-PlusICP and Premium Antisnake venoms (ASVs) against Echis ocellatus snake venom. The LD50 of the venom  in experimental mice was determined using probit analysis. The anti-lethality study of the Echitab Plus-ICP ASV at doses (3, 6, 9, 12 and 15 mL/kg)  and Premium ASV at doses (0.1, 0.2, 0.3, 0.4, and 0.5 mL/kg) was carried out according to Theakston and Reid method. Three doses (0.4, 0.8,  and 1.2  mL/kg) of the venom were administered intramuscularly (i.m) and the Minimum Hemorrhagic Dose (MHD) was determined. The venom's LD50 and MHD  in experimental mice were 4 mg/kg and 0.4 mg/kg respectively. The Echitab Plus-ICP ASV at doses (3, 6, 9, and 15 mL/kg) and the Premium ASV at the  doses (0.1, 0.2, 0.3, and 0.4 mL/kg) produced 100% protection against lethality induced by the 2LD50 of the Echis ocellatus snake venom. However,  Echitab Plus-ICP ASV at a dose of 12 mL/kg and Premium ASV at the dose of 0.5 mL/kg produced 83% and 50% protection respectively. Furthermore,  Echitab-Plus-ICP and Premium ASVs at all doses produced statistically significant (p<0.05) reduction in hemorrhage-induced by 2MHD of the venom. Also,  an in-vitro hemolysis assay of the two ASVs showed significant (p<0.05) reduction in venom-induced red blood cells hemolysis. These findings suggest  that Echitab-Plus-ICP and Premium Anti-venoms are effective against envenomings caused by Echis ocellatus venom. Further experiments should be  conducted on these ASVs so as to study its necrotizing, myotoxic and pro-coagulant properties.


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eISSN: 2635-3490
print ISSN: 2476-8316