Exp Clin Endocrinol Diabetes 2019; 127(04): 203-214
DOI: 10.1055/s-0043-122382
Review
© Georg Thieme Verlag KG Stuttgart · New York

Effects of the Reactive Metabolite Methylglyoxal on Cellular Signalling, Insulin Action and Metabolism – What We Know in Mammals and What We Can Learn From Yeast

Johanna Zemva
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
,
Daniel Pfaff
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
2   German Cancer Research Center (DKFZ), Heidelberg, Germany
,
Jan B. Groener
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
4   German Center for Diabetes Research (DZD), München-Neuherberg, Germany
,
Thomas Fleming
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
4   German Center for Diabetes Research (DZD), München-Neuherberg, Germany
,
Stephan Herzig
3   Joint Heidelberg-IDC Translational Diabetes Program, Dept. Inner Medicine I, Heidelberg University Hospital, Germany
5   Institute for Diabetes and Cancer IDC, Helmholtz Center Munich, Germany
,
Aurelio Teleman
2   German Cancer Research Center (DKFZ), Heidelberg, Germany
,
Peter P. Nawroth
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
3   Joint Heidelberg-IDC Translational Diabetes Program, Dept. Inner Medicine I, Heidelberg University Hospital, Germany
4   German Center for Diabetes Research (DZD), München-Neuherberg, Germany
,
Jens Tyedmers
1   Department of Medicine I and Clinical Chemistry, Heidelberg University Hospital, Heidelberg, Germany
› Author Affiliations
Further Information

Publication History

received 11 July 2017
revised29 September 2017

accepted 06 November 2017

Publication Date:
08 February 2018 (online)

Abstract

Levels of reactive metabolites such as reactive carbonyl and oxygen species are increased in patients with diabetes mellitus. The most important reactive dicarbonyl species, methylglyoxal (MG), formed as by-product during glucose metabolism, is more and more recognized as a trigger for the development and progression of diabetic complications. Although it is clear that MG provokes toxic effects, it is currently not well understood what cellular changes MG induces on a molecular level that may lead to pathophysiological conditions found in long-term diabetic complications. Here we review the current knowledge about the molecular effects that MG can induce in a cell. Within the mammalian system, we will focus mostly on the metabolic effects MG exerts when applied systemically to rodents or when applied in vitro to pancreatic β-cells and adipocytes. Due to the common limitations associated with complex model organisms, we then summarize how yeast as a very simple model organism can help to gain valuable comprehensive information on general defence pathways cells exert in response to MG stress. Pioneering studies in additional rather simple eukaryotic model organisms suggest that many cellular reactions in response to MG are highly conserved throughout evolution.

 
  • References

  • 1 Forbes JM, Cooper ME. Mechanisms of diabetic complications. Physiological reviews 2013; 93: 137-188
  • 2 Giacco F, Brownlee M. Oxidative stress and diabetic complications. Circulation research 2010; 107: 1058-1070
  • 3 Singh R, Barden A, Mori T. et al. Advanced glycation end-products: A review. Diabetologia 2001; 44: 129-146
  • 4 Yamagishi S, Maeda S, Matsui T. et al. Role of advanced glycation end products (AGEs) and oxidative stress in vascular complications in diabetes. Biochimica et biophysica acta 2012; 1820: 663-671
  • 5 Bierhaus A, Schiekofer S, Schwaninger M. et al. Diabetes-associated sustained activation of the transcription factor nuclear factor-kappaB. Diabetes 2001; 50: 2792-2808
  • 6 Brings S, Fleming T, Freichel M. et al. Dicarbonyls and advanced glycation end-products in the development of diabetic complications and targets for intervention. Int J Mol Sci 2017; 18 DOI: 10.3390/ijms18050984.
  • 7 Monnier VM, Sell DR, Genuth S. Glycation products as markers and predictors of the progression of diabetic complications. Annals of the New York Academy of Sciences 2005; 1043: 567-581
  • 8 Nowotny K, Jung T, Hohn A. et al. Advanced glycation end products and oxidative stress in type 2 diabetes mellitus. Biomolecules 2015; 5: 194-222
  • 9 Ahmed N, Thornalley PJ. Advanced glycation endproducts: What is their relevance to diabetic complications?. Diabetes, obesity & metabolism 2007; 9: 233-245
  • 10 Dhar A, Desai KM, Wu L. Alagebrium attenuates acute methylglyoxal-induced glucose intolerance in Sprague-Dawley rats. Br J Pharmacol 2010; 159: 166-175
  • 11 Sandu O, Song K, Cai W. et al. Insulin resistance and type 2 diabetes in high-fat-fed mice are linked to high glycotoxin intake. Diabetes 2005; 54: 2314-2319
  • 12 Cai W, Ramdas M, Zhu L. et al. Oral advanced glycation endproducts (AGEs) promote insulin resistance and diabetes by depleting the antioxidant defenses AGE receptor-1 and sirtuin 1. Proc Natl Acad Sci U S A 2012; 109: 15888-15893
  • 13 Nigro C, Raciti GA, Leone A. et al. Methylglyoxal impairs endothelial insulin sensitivity both in vitro and in vivo. Diabetologia 2014; 57: 1485-1494
  • 14 Dhar A, Dhar I, Jiang B. et al. Chronic methylglyoxal infusion by minipump causes pancreatic beta-cell dysfunction and induces type 2 diabetes in Sprague-Dawley rats. Diabetes 2011; 60: 899-908
  • 15 Hanssen NM, Stehouwer CD, Schalkwijk CG. Methylglyoxal and glyoxalase I in atherosclerosis. Biochemical Society transactions 2014; 42: 443-449
  • 16 Roesen P, Ferber P, Tschoepe D. Macrovascular disease in diabetes: current status. Experimental and clinical endocrinology & diabetes: official journal, German Society of Endocrinology [and] German Diabetes Association 2001; 109 (Suppl. 02) S474-S486
  • 17 Zheng F, He C, Cai W. et al. Prevention of diabetic nephropathy in mice by a diet low in glycoxidation products. Diabetes Metab Res Rev 2002; 18: 224-237
  • 18 Coughlan MT, Thorburn DR, Penfold SA. et al. RAGE-induced cytosolic ROS promote mitochondrial superoxide generation in diabetes. J Am Soc Nephrol 2009; 20: 742-752
  • 19 Morcos M, Sayed AA, Bierhaus A. et al. Activation of tubular epithelial cells in diabetic nephropathy. Diabetes 2002; 51: 3532-3544
  • 20 Berner AK, Brouwers O, Pringle R. et al. Protection against methylglyoxal-derived AGEs by regulation of glyoxalase 1 prevents retinal neuroglial and vasodegenerative pathology. Diabetologia 2012; 55: 845-854
  • 21 Curtis TM, Hamilton R, Yong PH. et al. Muller glial dysfunction during diabetic retinopathy in rats is linked to accumulation of advanced glycation end-products and advanced lipoxidation end-products. Diabetologia 2011; 54: 690-698
  • 22 Bierhaus A, Fleming T, Stoyanov S. et al. Methylglyoxal modification of Nav1.8 facilitates nociceptive neuron firing and causes hyperalgesia in diabetic neuropathy. Nature medicine 2012; 18: 926-933
  • 23 Bierhaus A, Haslbeck KM, Humpert PM. et al. Loss of pain perception in diabetes is dependent on a receptor of the immunoglobulin superfamily. J Clin Invest 2004; 114: 1741-1751
  • 24 Matafome P, Rodrigues T, Sena C. et al. Methylglyoxal in metabolic disorders: Facts, myths, and promises. Med Res Rev 2017; 37: 368-403
  • 25 Rabbani N, Thornalley PJ. Methylglyoxal, glyoxalase 1 and the dicarbonyl proteome. Amino acids 2012; 42: 1133-1142
  • 26 Rabbani N, Thornalley PJ. Dicarbonyl stress in cell and tissue dysfunction contributing to ageing and disease. Biochemical and biophysical research communications 2015; 458: 221-226
  • 27 Rabbani N, Thornalley PJ. Dicarbonyl proteome and genome damage in metabolic and vascular disease. Biochemical Society transactions 2014; 42: 425-432
  • 28 Rabbani N, Thornalley PJ. Glyoxalase in diabetes, obesity and related disorders. Seminars in cell & developmental biology 2011; 22: 309-317
  • 29 McLellan AC, Thornalley PJ, Benn J. et al. Glyoxalase system in clinical diabetes mellitus and correlation with diabetic complications. Clin Sci (Lond) 1994; 87: 21-29
  • 30 Wang H, Meng QH, Gordon JR. et al. Proinflammatory and proapoptotic effects of methylglyoxal on neutrophils from patients with type 2 diabetes mellitus. Clin Biochem 2007; 40: 1232-1239
  • 31 Fleming T, Nawroth PP. Reactive metabolites as a cause of late diabetic complications. Biochemical Society transactions 2014; 42: 439-442
  • 32 Inoue Y, Maeta K, Nomura W. Glyoxalase system in yeasts: structure, function, and physiology. Seminars in cell & developmental biology 2011; 22: 278-284
  • 33 Giacco F, Du X, D'Agati VD. et al. Knockdown of glyoxalase 1 mimics diabetic nephropathy in nondiabetic mice. Diabetes 2014; 63: 291-299
  • 34 Kim MJ, Kim DW, Lee BR. et al. Transduced Tat-glyoxalase protein attenuates streptozotocin-induced diabetes in a mouse model. Biochemical and biophysical research communications 2013; 430: 294-300
  • 35 Chen SJ, Aikawa C, Matsui T. Quantitative analysis of methylglyoxal, glyoxal and free advanced glycation end-products in the plasma of Wistar rats during the oral glucose tolerance test. Biol Pharm Bull 2015; 38: 336-339
  • 36 Hagiwara S, Gohda T, Tanimoto M. et al. Effects of pyridoxamine (K-163) on glucose intolerance and obesity in high-fat diet C57BL/6 J mice. Metabolism 2009; 58: 934-945
  • 37 Voziyan PA, Hudson BG. Pyridoxamine as a multifunctional pharmaceutical: targeting pathogenic glycation and oxidative damage. Cell Mol Life Sci 2005; 62: 1671-1681
  • 38 Hofmann SM, Dong HJ, Li Z. et al. Improved insulin sensitivity is associated with restricted intake of dietary glycoxidation products in the db/db mouse. Diabetes 2002; 51: 2082-2089
  • 39 Cai W, He JC, Zhu L. et al. Reduced oxidant stress and extended lifespan in mice exposed to a low glycotoxin diet: association with increased AGER1 expression. Am J Pathol 2007; 170: 1893-1902
  • 40 Lu C, He JC, Cai W. et al. Advanced glycation endproduct (AGE) receptor 1 is a negative regulator of the inflammatory response to AGE in mesangial cells. Proc Natl Acad Sci U S A 2004; 101: 11767-11772
  • 41 Cai W, He JC, Zhu L. et al. AGE-receptor-1 counteracts cellular oxidant stress induced by AGEs via negative regulation of p66shc-dependent FKHRL1 phosphorylation. Am J Physiol Cell Physiol 2008; 294: C145-C152
  • 42 Cai W, Uribarri J, Zhu L. et al. Oral glycotoxins are a modifiable cause of dementia and the metabolic syndrome in mice and humans. Proc Natl Acad Sci USA 2014; 111: 4940-4945
  • 43 Vlassara H, Uribarri J. Advanced glycation end products (AGE) and diabetes: Cause, effect, or both?. Curr Diab Rep 2014; 14: 453
  • 44 Roncero-Ramos I, Delgado-Andrade C, Tessier FJ. et al. Metabolic transit of N(epsilon)-carboxymethyl-lysine after consumption of AGEs from bread crust. Food Funct 2013; 4: 1032-1039
  • 45 Guilbaud A, Niquet-Leridon C, Boulanger E. et al. How can diet affect the accumulation of advanced glycation end-products in the human body?. Foods 2016; 5 DOI: 10.3390/foods5040084.
  • 46 Cheng AS, Cheng YH, Lee CY. et al. Resveratrol protects against methylglyoxal-induced hyperglycemia and pancreatic damage in vivo. Nutrients 2015; 7: 2850-2865
  • 47 Yu W, Fu YC, Wang W. Cellular and molecular effects of resveratrol in health and disease. J Cell Biochem 2012; 113: 752-759
  • 48 Xue M, Rabbani N, Momiji H. et al. Transcriptional control of glyoxalase 1 by Nrf2 provides a stress-responsive defence against dicarbonyl glycation. The Biochemical journal 2012; 443: 213-222
  • 49 Jang S, Kwon DM, Kwon K. et al. Generation and characterization of mouse knockout for glyoxalase 1. Biochemical and biophysical research communications 2017; DOI: 10.1016/j.bbrc.2017.06.063.
  • 50 Wortmann M, Hakimi M, Fleming T. et al. A Glyoxalase-1 knockdown does not have major short term effects on energy expenditure and atherosclerosis in mice. J Diabetes Res 2016; 2016: 2981639
  • 51 Morgenstern J, Fleming T, Schumacher D. et al. Loss of glyoxalase 1 induces compensatory mechanism to achieve dicarbonyl detoxification in mammalian schwann cells. The Journal of biological chemistry 2017; 292: 3224-3238
  • 52 Sheader EA, Benson RS, Best L. Cytotoxic action of methylglyoxal on insulin-secreting cells. Biochemical pharmacology 2001; 61: 1381-1386
  • 53 Ohsugi M, Cras-Meneur C, Zhou Y. et al. Reduced expression of the insulin receptor in mouse insulinoma (MIN6) cells reveals multiple roles of insulin signaling in gene expression, proliferation, insulin content, and secretion. The Journal of biological chemistry 2005; 280: 4992-5003
  • 54 Ohsugi M, Cras-Meneur C, Zhou Y. et al. Glucose and insulin treatment of insulinoma cells results in transcriptional regulation of a common set of genes. Diabetes 2004; 53: 1496-1508
  • 55 da Silva Xavier G, Varadi A, Ainscow EK. et al. Regulation of gene expression by glucose in pancreatic beta -cells (MIN6) via insulin secretion and activation of phosphatidylinositol 3'-kinase. The Journal of biological chemistry 2000; 275: 36269-36277
  • 56 Kulkarni RN, Bruning JC, Winnay JN. et al. Tissue-specific knockout of the insulin receptor in pancreatic beta cells creates an insulin secretory defect similar to that in type 2 diabetes. Cell 1999; 96: 329-339
  • 57 Best L, Thornalley PJ. Trioses and related substances: tools for the study of pancreatic beta-cell function. Biochemical pharmacology 1999; 57: 583-588
  • 58 Cook LJ, Davies J, Yates AP. et al. Effects of methylglyoxal on rat pancreatic beta-cells. Biochemical pharmacology 1998; 55: 1361-1367
  • 59 Fiory F, Lombardi A, Miele C. et al. Methylglyoxal impairs insulin signalling and insulin action on glucose-induced insulin secretion in the pancreatic beta cell line INS-1E. Diabetologia 2011; 54: 2941-2952
  • 60 Zhao Z, Zhao C, Zhang XH. et al. Advanced glycation end products inhibit glucose-stimulated insulin secretion through nitric oxide-dependent inhibition of cytochrome c oxidase and adenosine triphosphate synthesis. Endocrinology 2009; 150: 2569-2576
  • 61 Bo J, Xie S, Guo Y. et al. Methylglyoxal Impairs Insulin Secretion of Pancreatic beta-Cells through Increased Production of ROS and Mitochondrial Dysfunction Mediated by Upregulation of UCP2 and MAPKs. J Diabetes Res 2016; 2016: 2029854
  • 62 Chan CB, Saleh MC, Koshkin V. et al. Uncoupling protein 2 and islet function. Diabetes 2004; 53 (Suppl. 01) S136-S142
  • 63 Chan CB, MacDonald PE, Saleh MC. et al. Overexpression of uncoupling protein 2 inhibits glucose-stimulated insulin secretion from rat islets. Diabetes 1999; 48: 1482-1486
  • 64 Liu J, Li J, Li WJ. et al. The role of uncoupling proteins in diabetes mellitus. J Diabetes Res 2013; 2013: 585897
  • 65 Gao Y, Liao G, Xiang C. et al. Effects of phycocyanin on INS-1 pancreatic beta-cell mediated by PI3K/Akt/FoxO1 signaling pathway. Int J Biol Macromol 2016; 83: 185-194
  • 66 Gao Y, Liu C, Wan G. et al. Phycocyanin prevents methylglyoxal-induced mitochondrial-dependent apoptosis in INS-1 cells by Nrf2. Food Funct 2016; 7: 1129-1137
  • 67 Chang TJ, Tseng HC, Liu MW. et al. Glucagon-like peptide-1 prevents methylglyoxal-induced apoptosis of beta cells through improving mitochondrial function and suppressing prolonged AMPK activation. Sci Rep 2016; 6: 23403
  • 68 Jia X, Wu L. Accumulation of endogenous methylglyoxal impaired insulin signaling in adipose tissue of fructose-fed rats. Mol Cell Biochem 2007; 306: 133-139
  • 69 Wu CH, Huang HW, Huang SM. et al. AGE-induced interference of glucose uptake and transport as a possible cause of insulin resistance in adipocytes. J Agric Food Chem 2011; 59: 7978-7984
  • 70 Afridi SK, Aftab MF, Murtaza M. et al. A new glycotoxins inhibitor attenuates insulin resistance in liver and fat cells. Biochemical and biophysical research communications 2016; 476: 188-195
  • 71 Zemva J, Schubert M. The role of neuronal insulin/insulin-like growth factor-1 signaling for the pathogenesis of Alzheimer's disease: possible therapeutic implications. CNS Neurol Disord Drug Targets 2014; 13: 322-337
  • 72 Yuan X, Xu C, Pan Z. et al. Butylated hydroxyanisole regulates ARE-mediated gene expression via Nrf2 coupled with ERK and JNK signaling pathway in HepG2 cells. Mol Carcinog 2006; 45: 841-850
  • 73 Keum YS, Yu S, Chang PP. et al. Mechanism of action of sulforaphane: inhibition of p38 mitogen-activated protein kinase isoforms contributing to the induction of antioxidant response element-mediated heme oxygenase-1 in human hepatoma HepG2 cells. Cancer Res 2006; 66: 8804-8813
  • 74 Eijkelenboom A, Burgering BM. FOXOs: signalling integrators for homeostasis maintenance. Nat Rev Mol Cell Biol 2013; 14: 83-97
  • 75 Hoon S, Gebbia M, Costanzo M. et al. A global perspective of the genetic basis for carbonyl stress resistance. G3 (Bethesda) 2011; 1: 219-231
  • 76 Aguilera J, Prieto JA. The Saccharomyces cerevisiae aldose reductase is implied in the metabolism of methylglyoxal in response to stress conditions. Current genetics 2001; 39: 273-283
  • 77 Maeta K, Mori K, Takatsume Y. et al. Diagnosis of cell death induced by methylglyoxal, a metabolite derived from glycolysis, in Saccharomyces cerevisiae. FEMS microbiology letters 2005; 243: 87-92
  • 78 Aguilera J, Prieto JA. Yeast cells display a regulatory mechanism in response to methylglyoxal. FEMS yeast research 2004; 4: 633-641
  • 79 Maeta K, Izawa S, Okazaki S. et al. Activity of the Yap1 transcription factor in Saccharomyces cerevisiae is modulated by methylglyoxal, a metabolite derived from glycolysis. Molecular and cellular biology 2004; 24: 8753-8764
  • 80 Zemva J, Fink CA, Fleming TH. et al. Hormesis enables cells to handle accumulating toxic metabolites during increased energy flux. Redox Biol 2017; 13: 674-686
  • 81 Maeta K, Izawa S, Inoue Y. Methylglyoxal, a metabolite derived from glycolysis, functions as a signal initiator of the high osmolarity glycerol-mitogen-activated protein kinase cascade and calcineurin/Crz1-mediated pathway in Saccharomyces cerevisiae. The Journal of biological chemistry 2005; 280: 253-260
  • 82 Gomes RA, Sousa Silva M, Vicente Miranda H. et al. Protein glycation in Saccharomyces cerevisiae. Argpyrimidine formation and methylglyoxal catabolism. The FEBS journal 2005; 272: 4521-4531
  • 83 Gomes RA, Vicente Miranda H, Silva MS. et al. Yeast protein glycation in vivo by methylglyoxal. Molecular modification of glycolytic enzymes and heat shock proteins. The FEBS journal 2006; 273: 5273-5287
  • 84 Hoon S, Smith AM, Wallace IM. et al. An integrated platform of genomic assays reveals small-molecule bioactivities. Nature chemical biology 2008; 4: 498-506
  • 85 Inoue Y, Kimura A. Identification of the structural gene for glyoxalase I from Saccharomyces cerevisiae. The Journal of biological chemistry 1996; 271: 25958-25965
  • 86 Bito A, Haider M, Hadler I. et al. Identification and phenotypic analysis of two glyoxalase II encoding genes from Saccharomyces cerevisiae, GLO2 and GLO4, and intracellular localization of the corresponding proteins. The Journal of biological chemistry 1997; 272: 21509-21519
  • 87 Aguilera J, Rodriguez-Vargas S, Prieto JA. The HOG MAP kinase pathway is required for the induction of methylglyoxal-responsive genes and determines methylglyoxal resistance in Saccharomyces cerevisiae. Molecular microbiology 2005; 56: 228-239
  • 88 Inoue Y, Tsujimoto Y, Kimura A. Expression of the glyoxalase I gene of Saccharomyces cerevisiae is regulated by high osmolarity glycerol mitogen-activated protein kinase pathway in osmotic stress response. The Journal of biological chemistry 1998; 273: 2977-2983
  • 89 Albertyn J, Hohmann S, Thevelein JM. et al. GPD1, which encodes glycerol-3-phosphate dehydrogenase, is essential for growth under osmotic stress in Saccharomyces cerevisiae, and its expression is regulated by the high-osmolarity glycerol response pathway. Molecular and cellular biology 1994; 14: 4135-4144
  • 90 Norbeck J, Pahlman AK, Akhtar N. et al. Purification and characterization of two isoenzymes of DL-glycerol-3-phosphatase from Saccharomyces cerevisiae. Identification of the corresponding GPP1 and GPP2 genes and evidence for osmotic regulation of Gpp2p expression by the osmosensing mitogen-activated protein kinase signal transduction pathway. The Journal of biological chemistry 1996; 271: 13875-13881
  • 91 Phillips SA, Thornalley PJ. The formation of methylglyoxal from triose phosphates. Investigation using a specific assay for methylglyoxal. Eur J Biochem 1993; 212: 101-105
  • 92 Bankapalli K, Saladi S, Awadia SS. et al. Robust glyoxalase activity of Hsp31, a ThiJ/DJ-1/PfpI family member protein, is critical for oxidative stress resistance in Saccharomyces cerevisiae. The Journal of biological chemistry 2015; 290: 26491-26507
  • 93 Tsai CJ, Aslam K, Drendel HM. et al. Hsp31 Is a Stress Response Chaperone That Intervenes in the Protein Misfolding Process. The Journal of biological chemistry 2015; 290: 24816-24834
  • 94 Delaunay A, Pflieger D, Barrault MB. et al. A thiol peroxidase is an H2O2 receptor and redox-transducer in gene activation. Cell 2002; 111: 471-481
  • 95 Nomura W, Maeta K, Kita K. et al. Role of Gcn4 for adaptation to methylglyoxal in Saccharomyces cerevisiae: Methylglyoxal attenuates protein synthesis through phosphorylation of eIF2alpha. Biochemical and biophysical research communications 2008; 376: 738-742
  • 96 Nomura W, Maeta K, Kita K. et al. Methylglyoxal activates Gcn2 to phosphorylate eIF2alpha independently of the TOR pathway in Saccharomyces cerevisiae. Applied microbiology and biotechnology 2010; 86: 1887-1894
  • 97 Nomura W, Inoue Y. Methylglyoxal activates the target of rapamycin complex 2-protein kinase C signaling pathway in Saccharomyces cerevisiae. Molecular and cellular biology 2015; 35: 1269-1280
  • 98 Yoshida A, Wei D, Nomura W. et al. Reduction of glucose uptake through inhibition of hexose transporters and enhancement of their endocytosis by methylglyoxal in Saccharomyces cerevisiae. The Journal of biological chemistry 2012; 287: 701-711
  • 99 Roy A, Hashmi S, Li Z. et al. The glucose metabolite methylglyoxal inhibits expression of the glucose transporter genes by inactivating the cell surface glucose sensors Rgt2 and Snf3 in yeast. Mol Biol Cell 2016; 27: 862-871
  • 100 Morcos M, Du X, Pfisterer F. et al. Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegans. Aging cell 2008; 7: 260-269
  • 101 Schlotterer A, Kukudov G, Bozorgmehr F. et al. C. elegans as model for the study of high glucose- mediated life span reduction. Diabetes 2009; 58: 2450-2456
  • 102 Lee SJ, Murphy CT, Kenyon C. Glucose shortens the life span of C. elegans by downregulating DAF-16/FOXO activity and aquaporin gene expression. Cell metabolism 2009; 10: 379-391
  • 103 Mendler M, Schlotterer A, Morcos M. et al. Understanding diabetic polyneuropathy and longevity: What can we learn from the nematode Caenorhabditis elegans? Experimental and clinical endocrinology & diabetes: official journal. German Society of Endocrinology [and] German Diabetes Association 2012; 120: 182-183
  • 104 Wongchai K, Schlotterer A, Lin J. et al. Protective Effects of Liraglutide and Linagliptin in C. elegans as a New model for glucose-induced neurodegeneration. Hormone and metabolic research=Hormon- und Stoffwechselforschung=Hormones et metabolisme 2016; 48: 70-75
  • 105 Chaudhuri J, Bose N, Gong J. et al. A Caenorhabditis elegans model elucidates a conserved role for trpa1-nrf signaling in reactive alpha-dicarbonyl detoxification. Current biology: CB 2016; 26: 3014-3025
  • 106 Mendler M, Riedinger C, Schlotterer A. et al. Reduction in ins-7 gene expression in non-neuronal cells of high glucose exposed Caenorhabditis elegans protects from reactive metabolites, preserves neuronal structure and head motility, and prolongs lifespan. Journal of diabetes and its complications 2017; 31: 304-310
  • 107 Dietrich N, Kolibabka M, Busch S. et al. The DPP4 inhibitor linagliptin protects from experimental diabetic retinopathy. PLoS One 2016; 11: e0167853
  • 108 Garrido D, Rubin T, Poidevin M. et al. Fatty acid synthase cooperates with glyoxalase 1 to protect against sugar toxicity. PLoS genetics 2015; 11: e1004995
  • 109 Gnerer JP, Kreber RA, Ganetzky B. wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death. Proc Natl Acad Sci USA 2006; 103: 14987-14993
  • 110 Ahmed N, Battah S, Karachalias N. et al. Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency. Biochimica et biophysica acta 2003; 1639: 121-132
  • 111 Lee JY, Song J, Kwon K. et al. Human DJ-1 and its homologs are novel glyoxalases. Human molecular genetics 2012; 21: 3215-3225
  • 112 Richarme G, Mihoub M, Dairou J. et al. Parkinsonism-associated protein DJ-1/Park7 is a major protein deglycase that repairs methylglyoxal- and glyoxal-glycated cysteine, arginine, and lysine residues. The Journal of biological chemistry 2015; 290: 1885-1897
  • 113 Richarme G, Marguet E, Forterre P. et al. DJ-1 family Maillard deglycases prevent acrylamide formation. Biochemical and biophysical research communications 2016; 478: 1111-1116
  • 114 Richarme G, Liu C, Mihoub M. et al. Guanine glycation repair by DJ-1/Park7 and its bacterial homologs. Science (New York, NY) 2017; DOI: 10.1126/science.aag1095.
  • 115 Pfaff DH, Fleming T, Nawroth P. et al. Evidence Against a Role for the Parkinsonism-associated Protein DJ-1 in Methylglyoxal Detoxification. The Journal of biological chemistry 2017; 292: 685-690
  • 116 Richarme G, Dairou J. Parkinsonism-associated protein DJ-1 is a bona fide deglycase. Biochemical and biophysical research communications 2017; 483: 387-391
  • 117 Jorgens K, Stoll SJ, Pohl J. et al. High tissue glucose alters intersomitic blood vessels in zebrafish via methylglyoxal targeting the VEGF receptor signaling cascade. Diabetes 2015; 64: 213-225