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dc.creatorLiu,Chongbin
dc.creatorWang,Rui
dc.creatorZhang,Bo
dc.creatorHu,Chen
dc.creatorZhang,Hong
dc.date2013-01-01
dc.date.accessioned2019-05-02T21:22:12Z
dc.date.available2019-05-02T21:22:12Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602013000200011
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/82310
dc.descriptionLycopene is common in diet and known for its antioxidant activities. However, the impact of lycopene on iron metabolism is poorly investigated. In this study, we hypothesize that lycopene can prevent iron-mediated oxidative stress, proliferation and autophagy in liver and use a rat model of nutritional iron supplementation to confirm its intervention in these defence mechanisms. We found that iron supplementation induced cell proliferation predominantly in non parenchymal cells compared with hepatocytes, but not apoptosis. In addition, iron was accumulated within the hepatic lysosomes where it triggered autophagy as evidenced by the formation of autophagic vesicles detected by LC3-B staining. Iron supplementation also induced morphologic alterations of the mitochondrial membranes probably due to increased lipid peroxidation as indicated by elevated iron and malondialdehyde concentrations in serum and tissues. Lycopene reduced iron-catalyzed lipid peroxidation by decreasing the malondialdehyde level in the liver and colon and enhancing the total superoxide dismutase activities in serum and tissues. The result suggest that lycopene prevents iron-induced oxidative stress, proliferation and autophagy at both biochemical and histological levels due to its potent free radical scavenging and antioxidant properties.
dc.formattext/html
dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602013000200011
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.46 n.2 2013
dc.subjectAutophagy
dc.subjectiron supplementation
dc.subjectlycopene
dc.subjectoxidative stress
dc.subjectproliferation
dc.titleProtective effects of lycopene on oxidative stress, proliferation and autophagy in iron supplementation rats


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