Literature DB >> 16758767

Monosodium glutamate-induced oxidative damage and genotoxicity in the rat: modulatory role of vitamin C, vitamin E and quercetin.

E O Farombi1, O O Onyema.   

Abstract

Monosodium glutamate (MSG) continues to function as a flavor enhancer in West African and Asian diets. The present study examines the modulatory effects of dietary antioxidant vitamin C (VIT C), vitamin E (VIT E) and quercetin on MSG-induced oxidative damage in the liver, kidney and brain of rats. In addition, the effect of these antioxidants on the possible genotoxicity of MSG was investigated in a rat bone marrow micronuclei model. MSG administered intraperitoneally at a dose of 4 mg/g body wt markedly increase malondialdehyde (MDA) formation in the liver, the kidney and brain of rats. Simultaneous administration of VIT C, VIT E and quercetin to MSG-treated rats significantly reduced this increase in MDA induced by MSG. VIT E reduced lipid peroxidation most in the liver followed by VIT C and then quercetin, while VIT C and quercetin showed a greater ability to protect the brain from membrane damage than VIT E. The decreased glutathione (GSH) level elicited by MSG in the three organs corresponded with marked increase in the activity of glutathione-S-transferase (GST). While MSG increased (P < 0.001) the activities of superoxide dismutase and catalase in the liver, it decreased significantly the activities of these enzymes in the kidney and the brain. The three antioxidants were effective at ameliorating the effects of MSG on GSH levels and the enzymes in the three organs examined. While MSG increased the activity of glucose-6-phosphatase in the liver and kidneys of rats (P < 0.001), the activity of the enzyme was abysmally low in the brain. There were marked increases in the activities of alanine aminotransferase, aspartate aminotransferase and gamma-glutamyl transferase in rats treated with MSG. The antioxidants tested protected against MSG-induced liver toxicity significantly. MSG at a dose of 4 mg/g significantly (P < 0.01) induced the formation of micronucleated polychromatic erythrocytes (MNPCEs). Co-treatment of rats with VIT C and quercetin inhibited the induction of MNPCEs by MSG (P < 0.001). VIT E failed to protect against MSG-induced genotoxicity. The results indicate that dietary antioxidants have protective potential against oxidative stress induced by MSG and, in addition, suggest that active oxygen species may play an important role in its genotoxicity.

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Year:  2006        PMID: 16758767     DOI: 10.1191/0960327106ht621oa

Source DB:  PubMed          Journal:  Hum Exp Toxicol        ISSN: 0960-3271            Impact factor:   2.903


  24 in total

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Journal:  Acta Pharmacol Sin       Date:  2012-03-26       Impact factor: 6.150

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Journal:  Compr Rev Food Sci Food Saf       Date:  2019-05-08       Impact factor: 12.811

4.  Protective Effect of Calendula officinalis L. Flowers Against Monosodium Glutamate Induced Oxidative Stress and Excitotoxic Brain Damage in Rats.

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5.  Effect of different doses of monosodium glutamate on the thyroid follicular cells of adult male albino rats: a histological study.

Authors:  Hanaa A Khalaf; Eetmad A Arafat
Journal:  Int J Clin Exp Pathol       Date:  2015-12-01

6.  Protective effect of Trigonella foenum-graecum Linn. on monosodium glutamate-induced dyslipidemia and oxidative stress in rats.

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Journal:  Indian J Pharmacol       Date:  2013 Mar-Apr       Impact factor: 1.200

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8.  Aqueous Extract of Black Maca (Lepidium meyenii) on Memory Impairment Induced by Ovariectomy in Mice.

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Journal:  Evid Based Complement Alternat Med       Date:  2011-02-14       Impact factor: 2.629

9.  Prediabetic changes in gene expression induced by aspartame and monosodium glutamate in Trans fat-fed C57Bl/6 J mice.

Authors:  Kate S Collison; Nadine J Makhoul; Marya Z Zaidi; Angela Inglis; Bernard L Andres; Rosario Ubungen; Soad Saleh; Futwan A Al-Mohanna
Journal:  Nutr Metab (Lond)       Date:  2013-06-19       Impact factor: 4.169

10.  Quercetin protects islet β-cells from oxidation-induced apoptosis via Sirt3 in T2DM.

Authors:  Jian-Yun Wang; Ya-Xing Nie; Bing-Zheng Dong; Zhi-Chen Cai; Xuan-Kai Zeng; Lei Du; Xia Zhu; Xiao-Xing Yin
Journal:  Iran J Basic Med Sci       Date:  2021-05       Impact factor: 2.699

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