Silymarin, a natural antioxidant, protects cerebral cortex against manganese-induced neurotoxicity in adult rats
Identifieur interne : 001865 ( Main/Exploration ); précédent : 001864; suivant : 001866Silymarin, a natural antioxidant, protects cerebral cortex against manganese-induced neurotoxicity in adult rats
Auteurs : Yassine Chtourou [Tunisie] ; Hamadi Fetoui [Tunisie] ; Mediha Sefi [Tunisie] ; Khaled Trabelsi [Tunisie] ; Mohamed Barkallah [Tunisie] ; Tahia Boudawara [Tunisie] ; Héla Kallel [Tunisie] ; Najiba Zeghal [Tunisie]Source :
- BioMetals [ 0966-0844 ] ; 2010-12.
English descriptors
Abstract
Manganese (Mn) is an essential element for biological systems, nevertheless occupational exposure to high levels of Mn can lead to neurodegenerative disorders, characterized by serious oxidative and neurotoxic effects with similarities to Parkinson's disease. The aim of this study was to investigate the potential effects of silymarin (SIL), an antioxidant flavonoid, against manganese chloride induced neurotoxicity both in vivo (cerebral cortex of rats) and in vitro (Neuro2a cells). Twenty-eight male Wistar rats were randomly divided into four groups: the first group (C) received vehicle solution (i.p.) served as controls. The second group (Mn) received orally manganese chloride (20 mg/ml). The third group (Mn + SIL) received both Mn and SIL. The fourth group (SIL) received only SIL (100 mg/kg/day, i.p.). Animals exposed to Manganese chloride showed a significant increase in TBARS, NO, AOPP and PCO levels in cerebral cortex. These changes were accompanied by a decrease of enzymatic (SOD, CAT, GPx) and non-enzymatic (GSH, NpSH, Vit C) antioxidants. Co-administration of silymarin to Mn-treated rats significantly improved antioxidant enzyme activities and attenuated oxidative damages observed in brain tissue. The potential effect of SIL to prevent Mn induced neurotoxicity was also reflected by the microscopic study, indicative of its neuroprotective effects. We concluded that silymarin possesses neuroprotective potential, thus validating its use in alleviating manganese-induced neurodegenerative effects.
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DOI: 10.1007/s10534-010-9345-x
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</desc></org></tutelle></tutelles></hal:affiliation><country>Tunisie</country></affiliation></author></analytic><idno type="DOI">10.1007/s10534-010-9345-x</idno><series><title level="j">BioMetals</title><idno type="ISSN">0966-0844</idno><imprint><date type="datePub">2010-12</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="mix" xml:lang="en"><term> Cerebral cortex</term><term> Oxidative stress</term><term> Silymarin</term><term>Manganese toxicity</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Manganese (Mn) is an essential element for biological systems, nevertheless occupational exposure to high levels of Mn can lead to neurodegenerative disorders, characterized by serious oxidative and neurotoxic effects with similarities to Parkinson's disease. The aim of this study was to investigate the potential effects of silymarin (SIL), an antioxidant flavonoid, against manganese chloride induced neurotoxicity both in vivo (cerebral cortex of rats) and in vitro (Neuro2a cells). Twenty-eight male Wistar rats were randomly divided into four groups: the first group (C) received vehicle solution (i.p.) served as controls. The second group (Mn) received orally manganese chloride (20 mg/ml). The third group (Mn + SIL) received both Mn and SIL. The fourth group (SIL) received only SIL (100 mg/kg/day, i.p.). Animals exposed to Manganese chloride showed a significant increase in TBARS, NO, AOPP and PCO levels in cerebral cortex. These changes were accompanied by a decrease of enzymatic (SOD, CAT, GPx) and non-enzymatic (GSH, NpSH, Vit C) antioxidants. Co-administration of silymarin to Mn-treated rats significantly improved antioxidant enzyme activities and attenuated oxidative damages observed in brain tissue. The potential effect of SIL to prevent Mn induced neurotoxicity was also reflected by the microscopic study, indicative of its neuroprotective effects. We concluded that silymarin possesses neuroprotective potential, thus validating its use in alleviating manganese-induced neurodegenerative effects.</div></front></TEI><affiliations><list><country><li>Tunisie</li></country></list><tree><country name="Tunisie"><noRegion><name sortKey="Chtourou, Yassine" sort="Chtourou, Yassine" uniqKey="Chtourou Y" first="Yassine" last="Chtourou">Yassine Chtourou</name></noRegion><name sortKey="Barkallah, Mohamed" sort="Barkallah, Mohamed" uniqKey="Barkallah M" first="Mohamed" last="Barkallah">Mohamed Barkallah</name><name sortKey="Boudawara, Tahia" sort="Boudawara, Tahia" uniqKey="Boudawara T" first="Tahia" last="Boudawara">Tahia Boudawara</name><name sortKey="Fetoui, Hamadi" sort="Fetoui, Hamadi" uniqKey="Fetoui H" first="Hamadi" last="Fetoui">Hamadi Fetoui</name><name sortKey="Kallel, Hela" sort="Kallel, Hela" uniqKey="Kallel H" first="Héla" last="Kallel">Héla Kallel</name><name sortKey="Sefi, Mediha" sort="Sefi, Mediha" uniqKey="Sefi M" first="Mediha" last="Sefi">Mediha Sefi</name><name sortKey="Trabelsi, Khaled" sort="Trabelsi, Khaled" uniqKey="Trabelsi K" first="Khaled" last="Trabelsi">Khaled Trabelsi</name><name sortKey="Zeghal, Najiba" sort="Zeghal, Najiba" uniqKey="Zeghal N" first="Najiba" last="Zeghal">Najiba Zeghal</name></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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