Abayomi M Ajayi 1 , Benneth Ben-Azu 1 , Samuel A Onasanwo 2 , Olusegun Adeoluwa 1,3 , Anthony Eduviere 1,4 , Olusegun G Ademowo 1 . Show Affiliations »
Abstract
PURPOSE: Ocimum gratissimum L. leaves has been traditionally used for management of febrile illnesses and symptoms typified of sickness behavior. In this work we investigated the modulatory effect of flavonoid-rich fraction of O. gratissimum leaves (EAFOg) on sickness behavior, inflammatory and oxidative stress responses in LPS-challenged mice. METHOD: O. gratissimum leaf was first extracted with n-hexane, chloroform and methanol, and EAFOg was obtained by ethylacetate partitioning of a sequentially resultant methanol extract. The effect of EAFOg (25-100 mg/kg) on acute LPS-induced neurobehavioral impairment in an open field test (OFT) and depressive-like behavior in forced swimming test (FST) was investigated. Serum nitrite and TNF-α, as well as myeloperoxidase (MPO), malondialdehyde (MDA), and reduced glutathione (GSH) levels were determined in liver and brain tissues. RESULT: EAFOg prevented the reduction in locomotor and rearing activity in OFT and the increase in immobility time in FST. The fraction significantly attenuated the elevation of serum TNF- α and nitrite levels. EAFOg reversed LPS-induced increase in MDA, MPO, and nitrite levels and attenuated GSH depletion in liver and brain tissues of mice. CONCLUSION: Flavonoid-rich fraction of O. gratissimum leaf demonstrated significant modulation of LPS-induced sickness behavior, inflammatory and oxidative stress response in mice. This suggests an important therapeutic strategy in slowing down LPS-mediated hepatic and neuronal disease processes. © Georg Thieme Verlag KG Stuttgart · New York.
PURPOSE: Ocimum gratissimum L . leaves has been traditionally used for management of febrile illnesses and symptoms typified of sickness behavior. In this work we investigated the modulatory effect of flavonoid -rich fraction of O. gratissimum leaves (EAFOg ) on sickness behavior, inflammatory and oxidative stress responses in LPS -challenged mice . METHOD: O. gratissimum leaf was first extracted with n-hexane , chloroform and methanol , and EAFOg was obtained by ethylacetate partitioning of a sequentially resultant methanol extract. The effect of EAFOg (25-100 mg/kg) on acute LPS -induced neurobehavioral impairment in an open field test (OFT) and depressive -like behavior in forced swimming test (FST) was investigated. Serum nitrite and TNF-α, as well as myeloperoxidase (MPO ), malondialdehyde (MDA ), and reduced glutathione (GSH ) levels were determined in liver and brain tissues. RESULT: EAFOg prevented the reduction in locomotor and rearing activity in OFT and the increase in immobility time in FST. The fraction significantly attenuated the elevation of serum TNF- α and nitrite levels. EAFOg reversed LPS -induced increase in MDA , MPO , and nitrite levels and attenuated GSH depletion in liver and brain tissues of mice . CONCLUSION: Flavonoid -rich fraction of O. gratissimum leaf demonstrated significant modulation of LPS -induced sickness behavior, inflammatory and oxidative stress response in mice . This suggests an important therapeutic strategy in slowing down LPS -mediated hepatic and neuronal disease processes. © Georg Thieme Verlag KG Stuttgart · New York.
Entities: Chemical
Disease
Gene
Species
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Year: 2018
PMID: 30064151 DOI: 10.1055/a-0654-5042
Source DB: PubMed Journal: Drug Res (Stuttg) ISSN: 2194-9379