The role of insulin against hydrogen peroxide-induced oxidative damages in differentiated SH-SY5Y cells

References

• Ramalingam M, Kim SJ. Reactive oxygen/nitrogen species and their functional correlations in neurodegenerative diseases. J Neural Transm 2012;119:891–910
   PubMed Web of Science ®Google Scholar
• Crossthwaite AJ, Hasan S, Williams RJ. Hydrogen peroxide-mediated phosphorylation of ERK1/2, Akt/PKB and JNK in cortical neurones: dependence on Ca2+ and PI3-kinase. J Neurochem 2002;80:24–35
   Google Scholar
• Fahn S, Cohen G. The oxidant stress hypothesis in Parkinson's disease: evidence supporting it. Ann Neurol 1992;32:804–12
   PubMed Web of Science ®Google Scholar
• Halliwell B. Reactive oxygen species and the central nervous system. J Neurochem 1992;59:1609–23
   PubMed Web of Science ®Google Scholar
• Mahesh R, Jung HW, Kim YH, Park YK. Antioxidant and neuroprotective effects of JP05, a polyherbal medicine, on hydrogen peroxide-induced oxidative injury in Neuro-2a neuroblastoma cells. Curr Top Nutraceut Res 2011;9:13–23
   Web of Science ®Google Scholar
• Mahesh R, Kim SJ. The protective effects of insulin on hydrogen peroxide-induced oxidative stress in C6 glial cells. Biomol Ther 2009;17:395–402
   Web of Science ®Google Scholar
• Bozulic L, Hemmings BA. PIKKing on PKB: regulation of PKB activity by phosphorylation. Curr Opin Cell Biol 2009;21:256–61
   PubMed Web of Science ®Google Scholar
• Meier R, Hemmings BA. Regulation of protein kinase B. J Recept Signal Transduct Res 1999;19:121–8
   PubMed Web of Science ®Google Scholar
• Hart JR, Vogt PK. Phosphorylation of AKT: a mutational analysis. Oncotarget 2011;2:467–76
   Google Scholar
• Li F, Srinivasan A, Wang Y, et al. Cell-specific induction of apoptosis by microinjection of cytochrome c. Bcl-xL has activity independent of cytochrome c release. J Biol Chem 1997;272:30299–305
   PubMed Web of Science ®Google Scholar
• Bonneau B, Prudent J, Popgeorgiev N, Gillet G. Non-apoptotic roles of Bcl-2 family: the calcium connection. Biochim Biophys Acta 2013;1833:1755–65
   PubMed Web of Science ®Google Scholar
• Reaven GM. Banting Lecture 1988. Role of insulin resistance in human disease. 1988. Nutrition 1997;13:65–6; discussion 64
   Google Scholar
• Steiner DF, Oyer PE. The biosynthesis of insulin and a probable precursor of insulin by a human islet cell adenoma. Proc Natl Acad Sci USA 1967;57:473–80
   PubMed Web of Science ®Google Scholar
• Konrad D, Rudich A, Klip A. Insulin-mediated regulation of glucose metabolism. In: Kumar S, O’Rahilly S, eds. Insulin Resistance. England: John Wiley & Sons Ltd 2005;63–85
   Google Scholar
• Baura GD, Foster DM, Porte D, et al. Saturable transport of insulin from plasma into the central nervous system of dogs in vivo. A mechanism for regulated insulin delivery to the brain. J Clin Invest 1993;92:1824–30
   PubMed Web of Science ®Google Scholar
• Devaskar SU, Giddings SJ, Rajakumar PA, et al. Insulin gene expression and insulin synthesis in mammalian neuronal cells. J Biol Chem 1994;269:8445–54
   PubMed Web of Science ®Google Scholar
• Gerozissis K. Brain insulin, energy and glucose homeostasis; genes, environment and metabolic pathologies. Eur J Pharmacol 2008;585:38–49
   PubMed Web of Science ®Google Scholar
• Plum L, Schubert M, Bruning JC. The role of insulin receptor signaling in the brain. Trends Endocrinol Metab 2005;16:59–65
   PubMed Web of Science ®Google Scholar
• Zhao WQ, Alkon DL. Role of insulin and insulin receptor in learning and memory. Mol Cell Endocrinol 2001;177:125–34
   PubMed Web of Science ®Google Scholar
• Kim SJ, Han Y. Insulin inhibits AMPA-induced neuronal damage via stimulation of protein kinase B (Akt). J Neural Transm 2005;112:179–91
   PubMed Web of Science ®Google Scholar
• Grynkiewicz G, Poenie M, Tsien RY. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem 1985;260:3440–50
   PubMed Web of Science ®Google Scholar
• Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem 1979;95:351–8
   PubMed Web of Science ®Google Scholar
• Levine RL, Garland D, Oliver CN, et al. Determination of carbonyl content in oxidatively modified proteins. Methods Enzymol 1990;186:464–78
   PubMed Web of Science ®Google Scholar
• Ellman GL. Tissue sulfhydryl groups. Arch Biochem Biophys 1959;82:70–7
   PubMed Web of Science ®Google Scholar
• Zhang JL, Melton LD, Adaim A, Skinner MA. Cytoprotective effects of polyphenolics on H2O2-induced cell death in SH-SY5Y cells in relation to their antioxidant activities. Eur Food Res Technol 2008;228:123–31
   Google Scholar
• Jung CH, Hong MH, Kim JH, et al. Protective effect of a phenolic-rich fraction from Schisandra chinensis against H2O2-induced apoptosis in SH-SY5Y cells. J Pharm Pharmacol 2007;59:455–62
   Google Scholar
• Yu X, Li X, Jiang G, et al. Isradipine prevents rotenone-induced intracellular calcium rise that accelerates senescence in human neuroblastoma SH-SY5Y cells. Neuroscience 2013;246:243–53
   Google Scholar
• Wang W, Sun F, An Y, et al. Morroniside protects human neuroblastoma SH-SY5Y cells against hydrogen peroxide-induced cytotoxicity. Eur J Pharmacol 2009;613:19–23
   PubMed Web of Science ®Google Scholar
• Ye J, Han Y, Wang C, Yu W. Cytoprotective effect of polypeptide from Chlamys farreri on neuroblastoma (SH-SY5Y) cells following H2O2 exposure involves scavenging ROS and inhibition JNK phosphorylation. J Neurochem 2009;111:441–51
   PubMed Web of Science ®Google Scholar
• Bobermin LD, Souza DO, Gonçalves C-A, Quincozes-Santos A. Lipoic acid protects C6 cells against ammonia exposure through Na+–K+–Cl− co-transporter and PKC pathway. Toxicology In Vitro 2013;27:2041–8
   PubMed Web of Science ®Google Scholar
• Mahesh R, Jung HW, Han CH, et al. Joongpoongtang 05 (JP05) confers neuroprotection via anti-apoptotic activities in neuro-2a cells during oxygen–glucose deprivation and reperfusion. Toxicol In Vitro 2011;25:177–84
   PubMed Web of Science ®Google Scholar
• Mahesh R, Jung HW, Kim GW, et al. Cryptotanshinone from Salviae miltiorrhizae radix inhibits sodium-nitroprusside-induced apoptosis in neuro-2a cells. Phytother Res 2012;26:1211–9
   PubMed Web of Science ®Google Scholar
• Stephens L, Anderson K, Stokoe D, et al. Protein kinase B kinases that mediate phosphatidylinositol 3,4,5-trisphosphate-dependent activation of protein kinase B. Science 1998;279:710–4
   PubMed Web of Science ®Google Scholar
• Rommel C, Bodine SC, Clarke BA, et al. Mediation of IGF-1-induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways. Nat Cell Biol 2001;3:1009–13
   PubMed Web of Science ®Google Scholar
• Downward J. PI 3-kinase, Akt and cell survival. Semin Cell Dev Biol 2004;15:177–82
   PubMed Web of Science ®Google Scholar
• Sadidi M, Lentz SI, Feldman EL. Hydrogen peroxide-induced Akt phosphorylation regulates Bax activation. Biochimie 2009;91:577–85
   PubMed Web of Science ®Google Scholar
• Borner C. The Bcl-2 protein family: sensors and checkpoints for life-or-death decisions. Mol Immunol 2003;39:615–47
   PubMed Web of Science ®Google Scholar