FB2026_03 , released September 17, 2026
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Citation
Iorjiim, W.M., Makwin, L.L., Ipav, S.S., Omale, S. (2026). Kaempferol from Moringa oleifera L. increases longevity and ameliorates efavirenz-induced functional senescence in Drosophila melanogaster.  Toxicol Rep 17(): 102301.
FlyBase ID
FBrf0265778
Publication Type
Research paper
Abstract
Efavirenz acts against human immunodeficiency virus (HIV-1), induces functional senescence, and increases mortality in Drosophila melanogaster (Fruit fly). Kaempferol is a plant-derived flavonoid with neuroprotective and antioxidant properties. This study evaluated the protective effect of Kaempferol on efavirenz-induced functional senescence in D. melanogaster. Kaempferol was isolated from Moringa oleifera leaves. Adult flies (24-72 h old) were exposed to graded concentrations (1-1000 mg/10 g diet) to determine the median lethal concentration (LC50). Sublethal doses (5-50 mg/10 g diet) were used to assess longevity, acute toxicity, fecundity, locomotor performance, and biochemical parameters. For protective evaluation, flies were co-treated with efavirenz (5 mg/10 g diet) and kaempferol (10 or 20 mg/10 g diet) for 7 days. Survival, climbing ability, fecundity, antioxidant biomarkers, and acetylcholinesterase activity were subsequently measured. Kaempferol showed an LC50 of 338.60 mg/10 g diet. Additionally, it significantly improved survival, climbing ability, and reproductive capacity compared to control flies (P < 0.05). It also enhanced the antioxidant status in flies, as evidenced by a significant (P < 0.05) increase in total thiol levels, as well as glutathione S-transferase (GST), catalase (CAT), and superoxide dismutase (SOD) activities, alongside a decrease in malondialdehyde (MDA) concentration. Furthermore, Kaempferol mitigated efavirenz-induced mortality, climbing weakness, reproductive decline, and deficits in acetylcholinesterase (AChE) activity (P < 0.05). Overall, this study demonstrated the chemoprotective potential of Kaempferol against efavirenz-induced mortality and functional senescence in D. melanogaster through antioxidative mechanisms. This, to the best of our knowledge, has not been reported before.
PubMed ID
PubMed Central ID
PMC13319377 (PMC) (EuropePMC)
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Toxicol Rep
    Title
    Toxicology reports
    ISBN/ISSN
    2214-7500
    Data From Reference
    Chemicals (2)
    Human Disease Models (1)