FB2026_03 , released September 17, 2026
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Arogundade, T.T., Olatomide, O.D., Adeleye, D.A., Nwoke, E., Adim, V.C., Omotefe, A., Bayo-Olugbami, A.A., Omotoso, D.R., Gbadamosi, I. (2026). Quercetin parallels ascorbic acid in neuroprotection against manganese-induced toxicity in Drosophila melanogaster.  BMC Complement Med Ther 26(1): 195.
FlyBase ID
FBrf0265474
Publication Type
Research paper
Abstract
Quercetin (QCT) is a dietary flavonoid with reported antioxidant and neuroprotective properties, but direct comparisons with established antioxidants, such as ascorbic acid (AA), under chemically induced neurotoxic stress are limited. We compared Quercetin and AA in adult D. melanogaster using a manganese (Mn)-sensitized model to capture Parkinson-like motor and biochemical vulnerability. Treatment groups comprised: Control; Mn (15 mM); AA (10 mM); Quercetin 0.5 mM/3.0 mM; AA + Mn; Quercetin 0.5 mM/3.0 mM + Mn. Each vial represented an independent biological replicate (mixed sex); biochemical and genomic assays were performed using n = 4 vials/group. Outcomes included survival, locomotor performance (RING), redox endpoints (GSH/GSSG, H2O2, MDA, SOD, CAT), neuromodulators (AChE, dopamine), DNA fragmentation index (DFI), and advanced glycation end-products (AGEs). Omnibus tests (ANOVA or Kruskal-Wallis) were followed by Tukey HSD or Dunn-style pairwise comparisons; two pre-specified pooled contrasts were tested with Welch comparisons and effect sizes reported (mean differences, 95% CI, Cohen’s d); pooled p-values were adjusted (Holm, BH). Quercetin and AA produced comparable protective effects, as both preserved climbing behaviour and partially restored the redox balance versus Mn. One Tukey-adjusted pairwise result reached significance (Control vs. quercetin low + Mn for DFI, p_adj = 0.049). A pooled contrast showed reduced H2O2 for Quercetin (Q_all vs. AA_all: mean diff = 0.498 µmol·g[-1], 95% CI 0.153–0.844; Welch t(13.27) = 3.11, p = 0.0082; d ≈ 1.38), but this and other pooled signals did not survive conservative family-wise correction across all pooled tests. In conclusion, although they are overall comparable, our data suggest that quercetin may have a superior, specific effect on reducing H2O2 and protecting DNA integrity (DFI). These endpoints are now prioritized for confirmatory studies. [Figure: see text] The online version contains supplementary material available at 10.1186/s12906-026-05378-3. Quercetin and ascorbic acid (vitamin C) produced comparable neuroprotective effects in manganese-sensitized D. melanogaster, preserving locomotor performance and attenuating oxidative stress. A pooled contrast indicated a considerable reduction in H₂O₂ and DFI with Quercetin compared to AA, suggesting that H₂O₂ and DFI might be prioritized endpoints. Several endpoints (GSSG/GSH balance, AGEs) showed large effect sizes favouring quercetin in pooled contrasts. However, these signals did not survive conservative family-wise correction across the whole test family; therefore, the results are hypothesis-generating. The online version contains supplementary material available at 10.1186/s12906-026-05378-3.
PubMed ID
PubMed Central ID
PMC13202915 (PMC) (EuropePMC)
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    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    BMC Complement Med Ther
    Title
    BMC complementary medicine and therapies
    ISBN/ISSN
    2662-7671
    Data From Reference
    Chemicals (3)
    Genes (1)
    Human Disease Models (1)