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Published in: Neurotoxicity Research 3/2017

01-10-2017 | ORIGINAL ARTICLE

Methylglyoxal-Induced Protection Response and Toxicity: Role of Glutathione Reductase and Thioredoxin Systems

Authors: Ariana Ern Schmitz, Luiz Felipe de Souza, Barbara dos Santos, Pamela Maher, Fernanda Martins Lopes, Giovana Ferreira Londero, Fabio Klamt, Alcir Luiz Dafre

Published in: Neurotoxicity Research | Issue 3/2017

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Abstract

Thioredoxin (Trx) and glyoxalase (Glo) systems have been suggested to be molecular targets of methylglyoxal (MGO). This highly reactive endogenous compound has been associated with the development of neurodegenerative pathologies and cell death. In the present study, the glutathione (GSH), Trx, and Glo systems were investigated to understand early events (0.5–3 h) that may determine cell fate. It is shown for the first time that MGO treatment induces an increase in glutathione reductase (GR) protein in hippocampal slices (1 h) and HT22 nerve cells (0.5 and 2.5 h). Thioredoxin interacting protein (Txnip), thioredoxin reductase (TrxR), Glo1, and Glo2 were markedly increased (2- to 4-fold) in hippocampal slices and 1.2- to 1.3-fold in HT22 cells. This increase in protein levels in hippocampal slices was followed by a corresponding increase in GR, TrxR, and Glo1 activities, but not in HT22 cells. In these cells, GR and TrxR activities were decreased by MGO. This result is in agreement with the idea that MGO can affect the Trx/TrxR reducing system, and now we show that GR and Txnip can also be affected by MGO. Impairment in the GR or TrxR reducing capacity can impair peroxide removal by glutathione peroxidase and peroxiredoxin, as both peroxidases depend on reduced GSH and Trx, respectively. In this regard, inhibition of GR and TrxR by 2-AAPA or auranofin, respectively, potentiated MGO toxicity in differentiated SH-SY5Y cells. Overall, MGO not only triggers a clear defense response in hippocampal slices and HT22 cells but also impairs the Trx/TrxR and GSH/GR reducing couples in HT22 cells. The increased MGO toxicity caused by inhibition of GR and TrxR with specific inhibitors, or their inhibition by MGO treatment, supports the notion that both reducing systems are relevant molecular targets of MGO.
Literature
go back to reference Arnér ES, Zhong L, Holmgren A (1999) Preparation and assay of mammalian thioredoxin and thioredoxin reductase. Methods Enzymol 300:226–239CrossRefPubMed Arnér ES, Zhong L, Holmgren A (1999) Preparation and assay of mammalian thioredoxin and thioredoxin reductase. Methods Enzymol 300:226–239CrossRefPubMed
go back to reference Arscott LD, Veine DM, Williams CH (2000) Mixed disulfide with glutathione as an intermediate in the reaction catalyzed by glutathione reductase from yeast and as a major form of the enzyme in the cell. Biochemistry (Mosc) 39:4711–4721. doi:10.1021/bi9926431 CrossRef Arscott LD, Veine DM, Williams CH (2000) Mixed disulfide with glutathione as an intermediate in the reaction catalyzed by glutathione reductase from yeast and as a major form of the enzyme in the cell. Biochemistry (Mosc) 39:4711–4721. doi:10.​1021/​bi9926431 CrossRef
go back to reference Bevensee MO, Schwiening CJ, Boron WF (1995) Use of BCECF and propidium iodide to assess membrane integrity of acutely isolated CA1 neurons from rat hippocampus. J Neurosci Methods 58:61–75CrossRefPubMed Bevensee MO, Schwiening CJ, Boron WF (1995) Use of BCECF and propidium iodide to assess membrane integrity of acutely isolated CA1 neurons from rat hippocampus. J Neurosci Methods 58:61–75CrossRefPubMed
go back to reference Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254CrossRefPubMed Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72:248–254CrossRefPubMed
go back to reference Chang Y-C, Hsieh M-C, Wu H-J, Wu W-C, Kao Y-H (2015) Methylglyoxal, a reactive glucose metabolite, enhances autophagy flux and suppresses proliferation of human retinal pigment epithelial ARPE-19 cells. Toxicol in Vitro 29:1358–1368. doi:10.1016/j.tiv.2015.05.014 CrossRefPubMed Chang Y-C, Hsieh M-C, Wu H-J, Wu W-C, Kao Y-H (2015) Methylglyoxal, a reactive glucose metabolite, enhances autophagy flux and suppresses proliferation of human retinal pigment epithelial ARPE-19 cells. Toxicol in Vitro 29:1358–1368. doi:10.​1016/​j.​tiv.​2015.​05.​014 CrossRefPubMed
go back to reference Currais A, Farrokhi C, Dargusch R, Goujon-Svrzic M, Maher P (2016) Dietary glycemic index modulates the behavioral and biochemical abnormalities associated with autism spectrum disorder. Mol Psychiatry 21:426–436. doi:10.1038/mp.2015.64 CrossRefPubMed Currais A, Farrokhi C, Dargusch R, Goujon-Svrzic M, Maher P (2016) Dietary glycemic index modulates the behavioral and biochemical abnormalities associated with autism spectrum disorder. Mol Psychiatry 21:426–436. doi:10.​1038/​mp.​2015.​64 CrossRefPubMed
go back to reference Dafre AL, Schmitz AE, Maher P (2017) Methylglyoxal-induced AMPK activation leads to autophagic degradation of thioredoxin 1 and glyoxalase 2 in HT22 nerve cells. Free Radic Biol Med 108:270–279CrossRefPubMed Dafre AL, Schmitz AE, Maher P (2017) Methylglyoxal-induced AMPK activation leads to autophagic degradation of thioredoxin 1 and glyoxalase 2 in HT22 nerve cells. Free Radic Biol Med 108:270–279CrossRefPubMed
go back to reference Desai KM, Chang T, Wang H, Banigesh A, Dhar A, Liu J, Untereiner A, Wu L (2010) Oxidative stress and aging: is methylglyoxal the hidden enemy? Can J Physiol Pharmacol 88:273–284. doi:10.1139/Y10-001 CrossRefPubMed Desai KM, Chang T, Wang H, Banigesh A, Dhar A, Liu J, Untereiner A, Wu L (2010) Oxidative stress and aging: is methylglyoxal the hidden enemy? Can J Physiol Pharmacol 88:273–284. doi:10.​1139/​Y10-001 CrossRefPubMed
go back to reference Distler MG, Plant LD, Sokoloff G, Hawk AJ, Aneas I, Wuenschell GE, Termini J, Meredith SC, Nobrega MA, Palmer AA (2012) Glyoxalase 1 increases anxiety by reducing GABAA receptor agonist methylglyoxal. J Clin Invest 122:2306–2315. doi:10.1172/JCI61319 CrossRefPubMedPubMedCentral Distler MG, Plant LD, Sokoloff G, Hawk AJ, Aneas I, Wuenschell GE, Termini J, Meredith SC, Nobrega MA, Palmer AA (2012) Glyoxalase 1 increases anxiety by reducing GABAA receptor agonist methylglyoxal. J Clin Invest 122:2306–2315. doi:10.​1172/​JCI61319 CrossRefPubMedPubMedCentral
go back to reference Hawkes H-JK, Karlenius TC, Tonissen KF (2014) Regulation of the human thioredoxin gene promoter and its key substrates: a study of functional and putative regulatory elements. Biochim Biophys Acta BBA - Gen Subj 1840:303–314. doi:10.1016/j.bbagen.2013.09.013 CrossRef Hawkes H-JK, Karlenius TC, Tonissen KF (2014) Regulation of the human thioredoxin gene promoter and its key substrates: a study of functional and putative regulatory elements. Biochim Biophys Acta BBA - Gen Subj 1840:303–314. doi:10.​1016/​j.​bbagen.​2013.​09.​013 CrossRef
go back to reference Kimura R, Okouchi M, Fujioka H, Ichiyanagi A, Ryuge F, Mizuno T, Imaeda K, Okayama N, Kamiya Y, Asai K, Joh T (2009) Glucagon-like peptide-1 (GLP-1) protects against methylglyoxal-induced PC12 cell apoptosis through the PI3K/Akt/mTOR/GCLc/redox signaling pathway. Neurosci 162:1212–1219. doi:10.1016/j.neuroscience.2009.05.025 Kimura R, Okouchi M, Fujioka H, Ichiyanagi A, Ryuge F, Mizuno T, Imaeda K, Okayama N, Kamiya Y, Asai K, Joh T (2009) Glucagon-like peptide-1 (GLP-1) protects against methylglyoxal-induced PC12 cell apoptosis through the PI3K/Akt/mTOR/GCLc/redox signaling pathway. Neurosci 162:1212–1219. doi:10.​1016/​j.​neuroscience.​2009.​05.​025
go back to reference Lopes FM, Schröder R, da Frota ML Jr, Zanotto-Filho A, Müller CB, Pires AS, Meurer RT, Colpo GD, Gelain DP, Kapczinski F, JCF M, Fernandes Mda C, Klamt F (2010) Comparison between proliferative and neuron-like SH-SY5Y cells as an in vitro model for Parkinson disease studies. Brain Res 1337:85–94. doi:10.1016/j.brainres.2010.03.102 CrossRefPubMed Lopes FM, Schröder R, da Frota ML Jr, Zanotto-Filho A, Müller CB, Pires AS, Meurer RT, Colpo GD, Gelain DP, Kapczinski F, JCF M, Fernandes Mda C, Klamt F (2010) Comparison between proliferative and neuron-like SH-SY5Y cells as an in vitro model for Parkinson disease studies. Brain Res 1337:85–94. doi:10.​1016/​j.​brainres.​2010.​03.​102 CrossRefPubMed
go back to reference Lopes FM, da Motta LL, Bastiani MAD, Pfaffenseller B, Aguiar BW, de Souza LF, Zanatta G, Vargas DM, Schönhofen P, Londero GF, de Medeiros LM, Freire VN, Dafre AL, Castro MAA, Parsons RB, Klamt F (2017) RA differentiation enhances dopaminergic features, changes redox parameters, and increases dopamine transporter dependency in 6-hydroxydopamine-induced neurotoxicity in SH-SY5Y cells. Neurotox Res 1–15. doi:10.1007/s12640-016-9699-0 Lopes FM, da Motta LL, Bastiani MAD, Pfaffenseller B, Aguiar BW, de Souza LF, Zanatta G, Vargas DM, Schönhofen P, Londero GF, de Medeiros LM, Freire VN, Dafre AL, Castro MAA, Parsons RB, Klamt F (2017) RA differentiation enhances dopaminergic features, changes redox parameters, and increases dopamine transporter dependency in 6-hydroxydopamine-induced neurotoxicity in SH-SY5Y cells. Neurotox Res 1–15. doi:10.​1007/​s12640-016-9699-0
go back to reference Lubos E, Loscalzo J, Handy DE (2010) Glutathione peroxidase-1 in health and disease: from molecular mechanisms to therapeutic opportunities. Antioxid Redox Signal 15:1957–1997. doi:10.1089/ars.2010.3586 CrossRef Lubos E, Loscalzo J, Handy DE (2010) Glutathione peroxidase-1 in health and disease: from molecular mechanisms to therapeutic opportunities. Antioxid Redox Signal 15:1957–1997. doi:10.​1089/​ars.​2010.​3586 CrossRef
go back to reference Mitozo PA, De Souza LF, Loch-Neckel G, Flesch S, Maris AF, Figueiredo CP, Dos Santos ARS, Farina M, Dafre AL (2011) A study of the relative importance of the peroxiredoxin-, catalase-, and glutathione-dependent systems in neural peroxide metabolism. Free Radic Biol Med 51:69–77. doi:10.1016/j.freeradbiomed.2011.03.017 CrossRefPubMed Mitozo PA, De Souza LF, Loch-Neckel G, Flesch S, Maris AF, Figueiredo CP, Dos Santos ARS, Farina M, Dafre AL (2011) A study of the relative importance of the peroxiredoxin-, catalase-, and glutathione-dependent systems in neural peroxide metabolism. Free Radic Biol Med 51:69–77. doi:10.​1016/​j.​freeradbiomed.​2011.​03.​017 CrossRefPubMed
go back to reference Okouchi M, Okayama N, Aw T (2005) Hyperglycemia potentiates carbonyl stress-induced apoptosis in naive PC-12 cells: relationship to cellular redox and activator protease factor-1 expression. Curr Neurovasc Res 2:375–386. doi:10.2174/156720205774962665 Okouchi M, Okayama N, Aw T (2005) Hyperglycemia potentiates carbonyl stress-induced apoptosis in naive PC-12 cells: relationship to cellular redox and activator protease factor-1 expression. Curr Neurovasc Res 2:375–386. doi:10.​2174/​1567202057749626​65
go back to reference Qiao S, Dennis M, Song X, Vadysirisack DD, Salunke D, Nash Z, Yang Z, Liesa M, Yoshioka J, Matsuzawa S-I, Shirihai OS, Lee RT, Reed JC, Ellisen LW (2015) A REDD1/TXNIP pro-oxidant complex regulates ATG4B activity to control stress-induced autophagy and sustain exercise capacity. Nat Commun 6:7014. doi:10.1038/ncomms8014 CrossRefPubMedPubMedCentral Qiao S, Dennis M, Song X, Vadysirisack DD, Salunke D, Nash Z, Yang Z, Liesa M, Yoshioka J, Matsuzawa S-I, Shirihai OS, Lee RT, Reed JC, Ellisen LW (2015) A REDD1/TXNIP pro-oxidant complex regulates ATG4B activity to control stress-induced autophagy and sustain exercise capacity. Nat Commun 6:7014. doi:10.​1038/​ncomms8014 CrossRefPubMedPubMedCentral
go back to reference Rabbani N, Xue M, Thornalley PJ (2016a) Methylglyoxal-induced dicarbonyl stress in aging and disease: first steps towards glyoxalase 1-based treatments. Clin Sci 130:1677–1696. doi:10.1042/CS20160025 CrossRefPubMed Rabbani N, Xue M, Thornalley PJ (2016a) Methylglyoxal-induced dicarbonyl stress in aging and disease: first steps towards glyoxalase 1-based treatments. Clin Sci 130:1677–1696. doi:10.​1042/​CS20160025 CrossRefPubMed
go back to reference Racker E (1951) The mechanism of action of glyoxalase. J Biol Chem 190:685–696PubMed Racker E (1951) The mechanism of action of glyoxalase. J Biol Chem 190:685–696PubMed
go back to reference Rodnight R, Gonçalves CA, Leal R, Rocha E, Salbego CG, Wofchuk ST (1991) Chapter 11: Regional distribution and properties of an enzyme system in rat brain that phosphorylates ppH-47, an insoluble protein highly labelled in tissue slices from the hippocampus. In: Routtenberg WHG and A (ed) Progress in Brain Research. Elsevier, pp 157–167 Rodnight R, Gonçalves CA, Leal R, Rocha E, Salbego CG, Wofchuk ST (1991) Chapter 11: Regional distribution and properties of an enzyme system in rat brain that phosphorylates ppH-47, an insoluble protein highly labelled in tissue slices from the hippocampus. In: Routtenberg WHG and A (ed) Progress in Brain Research. Elsevier, pp 157–167
go back to reference Selenius M, Rundlöf A-K, Olm E, Fernandes AP, Björnstedt M (2010) Selenium and the selenoprotein thioredoxin reductase in the prevention, treatment and diagnostics of cancer. Antioxid Redox Signal 12:867–880. doi:10.1089/ars.2009.2884 CrossRefPubMed Selenius M, Rundlöf A-K, Olm E, Fernandes AP, Björnstedt M (2010) Selenium and the selenoprotein thioredoxin reductase in the prevention, treatment and diagnostics of cancer. Antioxid Redox Signal 12:867–880. doi:10.​1089/​ars.​2009.​2884 CrossRefPubMed
go back to reference Thornalley PJ (1996) Pharmacology of methylglyoxal: formation, modification of proteins and nucleic acids, and enzymatic detoxification—a role in pathogenesis and antiproliferative chemotherapy. Gen Pharmacol 27:565–573CrossRefPubMed Thornalley PJ (1996) Pharmacology of methylglyoxal: formation, modification of proteins and nucleic acids, and enzymatic detoxification—a role in pathogenesis and antiproliferative chemotherapy. Gen Pharmacol 27:565–573CrossRefPubMed
go back to reference Thornalley PJ (2003) Glyoxalase I-structure, function and a critical role in the enzymatic defence against glycation. Biochem Soc Trans 31:1343–1348CrossRefPubMed Thornalley PJ (2003) Glyoxalase I-structure, function and a critical role in the enzymatic defence against glycation. Biochem Soc Trans 31:1343–1348CrossRefPubMed
go back to reference Wang X, Desai K, Chang T, Wu L (2005) Vascular methylglyoxal metabolism and the development of hypertension. J Hypertens 23:1565–1573CrossRefPubMed Wang X, Desai K, Chang T, Wu L (2005) Vascular methylglyoxal metabolism and the development of hypertension. J Hypertens 23:1565–1573CrossRefPubMed
go back to reference Wang X-L, Lau WB, Yuan Y-X, Wang Y-J, Yi W, Christopher TA, Lopez BL, Liu H-R, Ma X-L (2010) Methylglyoxal increases cardiomyocyte ischemia-reperfusion injury via glycative inhibition of thioredoxin activity. Am J Physiol - Endocrinol Metab 299:E207–E214. doi:10.1152/ajpendo.00215.2010 PubMedPubMedCentral Wang X-L, Lau WB, Yuan Y-X, Wang Y-J, Yi W, Christopher TA, Lopez BL, Liu H-R, Ma X-L (2010) Methylglyoxal increases cardiomyocyte ischemia-reperfusion injury via glycative inhibition of thioredoxin activity. Am J Physiol - Endocrinol Metab 299:E207–E214. doi:10.​1152/​ajpendo.​00215.​2010 PubMedPubMedCentral
go back to reference Wu L, Juurlink BHJ (2002) Increased methylglyoxal and oxidative stress in hypertensive rat vascular smooth muscle cells. Hypertens Dallas Tex 1979 39:809–814 Wu L, Juurlink BHJ (2002) Increased methylglyoxal and oxidative stress in hypertensive rat vascular smooth muscle cells. Hypertens Dallas Tex 1979 39:809–814
go back to reference Xue M, Rabbani N, Momiji H, Imbasi P, Anwar MM, Kitteringham N, Park BK, Souma T, Moriguchi T, Yamamoto M, Thornalley PJ (2012) Transcriptional control of glyoxalase 1 by Nrf2 provides a stress-responsive defence against dicarbonyl glycation. Biochem J 443:213–222. doi:10.1042/BJ20111648 CrossRefPubMed Xue M, Rabbani N, Momiji H, Imbasi P, Anwar MM, Kitteringham N, Park BK, Souma T, Moriguchi T, Yamamoto M, Thornalley PJ (2012) Transcriptional control of glyoxalase 1 by Nrf2 provides a stress-responsive defence against dicarbonyl glycation. Biochem J 443:213–222. doi:10.​1042/​BJ20111648 CrossRefPubMed
go back to reference Yoshihara E, Masaki S, Matsuo Y, Chen Z, Tian H, Yodoi J (2014) Thioredoxin/Txnip: redoxisome, as a redox switch for the pathogenesis of diseases. Inflammation 4:514. doi:10.3389/fimmu.2013.00514 Yoshihara E, Masaki S, Matsuo Y, Chen Z, Tian H, Yodoi J (2014) Thioredoxin/Txnip: redoxisome, as a redox switch for the pathogenesis of diseases. Inflammation 4:514. doi:10.​3389/​fimmu.​2013.​00514
Metadata
Title
Methylglyoxal-Induced Protection Response and Toxicity: Role of Glutathione Reductase and Thioredoxin Systems
Authors
Ariana Ern Schmitz
Luiz Felipe de Souza
Barbara dos Santos
Pamela Maher
Fernanda Martins Lopes
Giovana Ferreira Londero
Fabio Klamt
Alcir Luiz Dafre
Publication date
01-10-2017
Publisher
Springer US
Published in
Neurotoxicity Research / Issue 3/2017
Print ISSN: 1029-8428
Electronic ISSN: 1476-3524
DOI
https://doi.org/10.1007/s12640-017-9738-5

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