Moringa oleifera Extract Extenuates Echis ocellatus Venom-Induced Toxicities, Histopathological Impairments and Inflammation via Enhancement of Nrf2 Expression in Rats

snakebite causes more fatalities than all other African snake species combined. reportedly possesses an antivenom property. Therefore, we evaluated the effectiveness of ethanol extract (MOE) against (EOV) toxicities. Thirty male rats were grouped as follows ( = 5): Group 1 (normal control received s...

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Veröffentlicht in:Pathophysiology (Amsterdam) 2021-03, Vol.28 (1), p.98-115
Hauptverfasser: Adeyi, Akindele O, Adeyemi, Sodiq O, Effiong, Enoh-Obong P, Ajisebiola, Babafemi S, Adeyi, Olubisi E, James, Adewale S
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Sprache:eng
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Zusammenfassung:snakebite causes more fatalities than all other African snake species combined. reportedly possesses an antivenom property. Therefore, we evaluated the effectiveness of ethanol extract (MOE) against (EOV) toxicities. Thirty male rats were grouped as follows ( = 5): Group 1 (normal control received saline), groups 2 to 6 were administered intraperitoneally, 0.22 mg/kg (LD50) of EOV. Group 2 was left untreated while group 3 to 6 were treated post-envenoming with 0.2 mL of polyvalent antivenom, 200, 400, and 600 mg/kg of MOE respectively. MOE significantly ( < 0.05) normalized the altered haematological indices and blood electrolytes profiles. MOE attenuated venom-induced cellular dysfunctions, characterized by a significant increase in NRF2, and concomitant downregulation of increased antioxidant enzymes (SOD and CAT) activities in the serum and heart of the treated rats. MOE normalized the elevated TNF-α and IL-1β in serum and heart tissues. Furthermore, the IgG titre value was significantly ( < 0.5) higher in the envenomed untreated group compared to the MOE-treated groups. Hemorrhagic, hemolytic and coagulant activities of the venom were strongly inhibited by the MOE dose, dependently. Lesions noticed on tissues of vital organs of untreated rats were abolished by MOE. Our findings substantiate the effectiveness of MOE as a potential remedy against EOV toxicities.
ISSN:1873-149X
0928-4680
1873-149X
DOI:10.3390/pathophysiology28010009