Indole-3-propionic acid mitigates chlorpyrifos-mediated neurotoxicity by modulating cholinergic and redox-regulatory systems, inflammatory stress, apoptotic responses and DNA damage in rats

dc.contributor.authorOwumi, S. E.
dc.contributor.authorAdedara, I. A.
dc.contributor.authorOyelere, A. K.
dc.date.accessioned2026-02-10T14:57:14Z
dc.date.issued2022
dc.description.abstractThis study probed the neuroprotective influence of indole-3-propionic acid (IPA) in rats exposed to chlorpyrifos (CPF) alone at 5 mg/kg body weight or co-administered with IPA at 12.5 and 25 mg/kg for 14 days. Behavioral data indicated that IPA significantly (p < 0.05) abated CPF-mediated anxiogenic-like behaviors with concomitant improvement in the locomotor and exploratory behaviors as substantiated by track plots and heat maps data. Also, IPA mitigated CPF-mediated diminution in cholinergic and antioxidant defense systems whereas it mark- edly improved thioredoxin level and thioredoxin reductase activity in cerebral and cerebellar tissues of the animals. Co-administration of IPA significantly enhanced anti-inflammatory cytokine, interleukin-10 but sup- pressed oxidative and inflammatory stress, caspase-9 and caspase-3 activation with concomitant reduction in 8- hydroxy-2'-deoxyguanosine (8-OHdG) level and histological damage. Collectively, IPA-mediated neuro- protection involves modulation of cholinergic and redox-regulatory systems, inflammatory stress, apoptotic re- sponses and DNA damage in cerebrum and cerebellum of rats.
dc.identifier.issn1382-6689
dc.identifier.otherui_art_owumi_indole_2022
dc.identifier.otherEnvironmental Toxicology and Pharmacology 89 (103786)
dc.identifier.urihttps://repository.ui.edu.ng/handle/123456789/12070
dc.language.isoen
dc.publisherElsevier B.V.
dc.subjectChlorpyrifos
dc.subjectIndole-3-propionic acid
dc.subjectAcetylcholinesterase
dc.subjectRedox-regulatory systems
dc.subject8-hydroxy-2'-deoxyguanosine
dc.titleIndole-3-propionic acid mitigates chlorpyrifos-mediated neurotoxicity by modulating cholinergic and redox-regulatory systems, inflammatory stress, apoptotic responses and DNA damage in rats
dc.typeArticle

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