Naringin protects memory impairment and mitochondrial oxidative damage against aluminum-induced neurotoxicity in rats

References

• Bondy SC. The neurotoxicity of environmental aluminum is still an issue. Neurotoxicology 2010;31(5):575–81.
   PubMed Web of Science ®Google Scholar
• Pratico D, Uryu K, Sung S, Aluminium modulates brain amyloidosis through oxidative stress in APP transgenic mice. FASEB J 2002;16(9):1138–40.
   PubMed Web of Science ®Google Scholar
• Rondeau V, Commenges D, Jacqmin-Gadda H, Dartigues JF. Relation between aluminium concentration in drinking water and Alzheimer's disease: 8 year follow up study. Am J Epidemiol 2000;152:59–66.
   PubMed Web of Science ®Google Scholar
• Kumar A, Dogra S, Prakash A. Protective effect of curcumin (Curcuma longa), against aluminium toxicity: possible behavioral and biochemical alterations in rats. Behav Brain Res 2009;205(2):384–90.
   PubMed Web of Science ®Google Scholar
• Miu AC, Benga O. Aluminium and Alzheimer's disease: a new look. J Alzheim Dis 2006;10:179–201.
   PubMed Web of Science ®Google Scholar
• Platt B, Fiddler G, Riedel G, Henderson Z. Aluminium toxicity in the rat brain: histochemical and immunocytochemical evidence. Brain Res Bull 2001;55:257–67.
   PubMed Web of Science ®Google Scholar
• Campbell A, Hamai D, Bondy SC. Differential toxicity of aluminium salts in human cell lines of neural origin: implications for neurodegeneration. Neurotoxicol 2001;22:63–71.
   PubMed Web of Science ®Google Scholar
• Exley C, Esiri MM. Severe cerebral congophilic angiopathy coincident with increased brain aluminium in a resident of Camelford, Cornwall, UK. J Neurol neurosurg Psychiatry 2006;77(7):877–9.
   PubMed Web of Science ®Google Scholar
• Blaylock RL. Aluminum induced immuno excitotoxicity in neurodevelopmental and neurodegenerative disorders. Curr Inorg Chem 2011;1(1):46–53.
   Google Scholar
• Kumar V, Bal A, Gill KD. Impairment of mitochondrial energy metabolism in different regions of rat brain following chronic exposure to aluminium. Brain Res 2008;1232:94–103.
   PubMed Web of Science ®Google Scholar
• Choe SC, Kim HS, Jeong TS, Naringin has an antiatherogenic effect with the inhibition of intercellular adhesion molecule-1 in hypercholesterolemic rabbits. J Cardiovasc Pharmacol 2001;38(6):947–55.
   Web of Science ®Google Scholar
• Jeon SM, Bok SH, Jang MK, Comparison of antioxidant effects of naringin and probucol in cholesterol fed rabbits. Clin Chim Acta 2002;317:181–90.
   PubMed Web of Science ®Google Scholar
• Kumar A, Dogra S, Prakash A. Possible effect of naringin a citrus flavonoid, against colchicine induced cognitive dysfunction and oxidative damage in rats. J Med Food 2010;(4):1–9.
   Google Scholar
• Kumar A, Prakash A, Dogra S. Naringin alleviates cognitive impairment, mitochondrial dysfunction and oxidative stress induced by d-galactose in mice. Food Chem Toxicol 2010;48(2):626–32.
   PubMed Web of Science ®Google Scholar
• Jagetia GC, Reddy TK. The grapefruit flavanone naringin protects against the radiation-induced genomic instability in the mouse bone marrow: a micronucleus study. Mutation Res 2002;519:37–48.
   PubMed Web of Science ®Google Scholar
• Jagetia GC, Venkatesha VA, Reddy TK. Naringin, a citrus flavonone, protects against radiation-induced chromosome damage in mouse bone marrow. Mutagenesis 2003;18: 337–43.
   PubMed Web of Science ®Google Scholar
• Jagetia GC, Reddy TK, Venkatesha VA, Kedlaya R. Influence of naringin on ferric iron induced oxidative damage in vitro. Clin Chim Acta 2004;347:189–97.
   PubMed Web of Science ®Google Scholar
• Jagetia A, Jagetia GC, Jha S. Naringin, a grapefruit flavanone, protects V79 cells against the bleomycin-induced genotoxicity and decline in survival. J Appl Toxicol 2007;27:122–32.
   PubMed Web of Science ®Google Scholar
• Jagetia GC, Reddy TK. Alleviation of iron induced oxidative stress by the grape fruit flavanone naringin in vitro. Chem Biol Interact 2011;190(2–3):121–8.
   Google Scholar
• Jagetia GC, Reddy TK. Modulation of radiation-induced alteration in the antioxidant status of mice by naringin. Life Sci 2005;77(7):780–94.
   PubMed Web of Science ®Google Scholar
• Prakash A, Kumar A. Effect of N-acetyl cysteine against aluminium-induced cognitive dysfunction and oxidative damage in rats. Basic Clin Pharmacol Toxicol 2009;105(2):98–104
   PubMed Web of Science ®Google Scholar
• Wills ED. Mechanism of lipid peroxide formation in animal tissues. Biochemical J 1966;99:667–76.
   PubMed Web of Science ®Google Scholar
• Green LC, Wagner DA, Glagowski J. Analysis of nitrate, nitrite and (15 N) nitrate in biological fluids. Anal Biochem 1982;126:131–8.
   PubMed Web of Science ®Google Scholar
• Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70–7.
   PubMed Web of Science ®Google Scholar
• Kono Y. Generation of Superoxide radical during auto-oxidation of hydroxylamine and an assay for Superoxide dismutase. Arch Biochem Biophys 1978;186:189–95.
   PubMed Web of Science ®Google Scholar
• Luck H. Catalase. In: Bergmeyer HJ, ed. Methods of enzymatic analysis. 3rd ed. New York: Academic Press; 1971;III:885–893.
   Google Scholar
• Habig WH, Jakoby WB. Assays for differentiation of glutathione-S-transferases. Methods Enzymol 1981;77:398–405.
   PubMedGoogle Scholar
• Ellman GL, Courtney V, Andres RM. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol 1961;7:88–95.
   PubMed Web of Science ®Google Scholar
• Gornall AG, Bardawill CT. David MM. Determination of serum proteins by means of Biuret reaction. J Biol Chem 1949;177:751–66.
   PubMed Web of Science ®Google Scholar
• King TE, Howard RL. Preparations and properties of soluble NADH dehydrogenases from cardiac muscle Methods Enzymol 1967;10:275–94.
   Google Scholar
• King TE. Preparation of succinate dehydrogenase and reconstitution of succinate oxidase Methods Enzymol 1967;10: 322–31.
   Google Scholar
• Liu Y, Peterson DA, Kimura H, Schubert D. Mechanisms of cellular 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolinium bromide (MTT) reduction J Neurochem 1997;69:581–93.
   PubMed Web of Science ®Google Scholar
• Sottocasa GL, Kuylenstierna B, Ernster L, Bergstrand A. An electron-transport system associated with the outer membrane of liver mitochondria. A biochemical and morphological study. J Cell Biol 1967;32:415–38.
   PubMed Web of Science ®Google Scholar
• Zumkley H, Bertram HP, Lison A, Aluminum, zinc and copper concentrations in plasma in chronic renal insufficiency. Clin Nephrol 1979;12:18–21.
   PubMed Web of Science ®Google Scholar
• Canales JJ, Corbalàn R, Montoliu C, Aluminium impairs the glutamate-nitric oxide-cGMP pathway in cultured neurons and in rat brain in vivo: molecular mechanisms and implications for neuropathology. J Inorgan Biochem 2001;87:63–9.
   PubMed Web of Science ®Google Scholar
• Yokel RA. The toxicology of aluminium in the brain: a review. Neurotoxicology 2000;21(5):813–28.
   PubMed Web of Science ®Google Scholar
• Rabe A, Moon HL, Shek J, Wisniewski HM. Learning deficit in immature rabbits with aluminium induced neurofibrillary changes. Exp Neurol 1982;76:441–6. doi:10.1016/ 0014-4886(82)90220-5.
   PubMed Web of Science ®Google Scholar
• Bolla KI, Briefel G, Spector D, Neurocognitive effects of aluminum. Arch Neurol 1992;49(10):1021–6.
   PubMedGoogle Scholar
• Reddy PH. Mitochondrial dysfunction in aging and Alzheimer's disease: strategies to protect neurons. Antioxid Redox Signal 2007;9:1647–58.
   PubMed Web of Science ®Google Scholar
• Tomljenovic L. Aluminum and Alzheimer's disease: after a century of controversy, is their a plausable link? J Alzheimer's Dis 2011;23:567–98.
   PubMed Web of Science ®Google Scholar
• Rajadurai M, Prince PSM. Preventive effect of naringin on lipid peroxides and antioxidants in isoproterenol –induced cardiotoxicity in Wistar rats: biochemical and histopathological evidences. Toxicol 2006;228:259–68.
   PubMed Web of Science ®Google Scholar
• Jeon SM, Park YB, Choi MS. Antihypercholesterolaemic property of naringin alters plasma and tissue lipids, cholesterol regulating enzymes, fecal sterol and tissue morphology in rabbits. Clin Nutr 2004;23:1025–34.
   PubMed Web of Science ®Google Scholar
• Choi SY, Ko HC, Ko SY, Correlation between flavonoid content and the NO production inhibitory activity of peel extracts from various citrus fruits. Biol Pharm Bull 2007;30(4):772–8.
   PubMed Web of Science ®Google Scholar
• Mercer LD, Kelly BL, Horne MK, Beart PM. Dietary polyphenols protect dopamine neurons from oxidative insults and apoptosis: investigations in primary mesencephalic cultures. Biochem Pharmacol 2005;69:339–45.
   PubMed Web of Science ®Google Scholar
• Kroyer G. The antioxidant activity of citrus fruit peels. Z Ernahrungswiss 1986;25:63–9.
   PubMedGoogle Scholar
• Zatta P, Ibn-Lkhayat M, Zambenedetti P, In vivo and in vitro effects of aluminium on the activity of mouse brain acetylcholinesterase. Brain Res Bull 2002;59:41–5.
   PubMed Web of Science ®Google Scholar
• Kumar S. Biphasic effect of aluminium on cholinergic enzyme of rat brain. Neurosci Lett 1998;248:121–3.
   PubMed Web of Science ®Google Scholar
• Gulya K, Rakonczay Z, Kasa P. Cholinotoxic effects of aluminium in rat brain. J Neurochem 1990;54: 1020–6.
   PubMed Web of Science ®Google Scholar