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Published in: Diabetologia 8/2015

Open Access 01-08-2015 | Commentary

Vascular AGE-ing by methylglyoxal: the past, the present and the future

Author: Casper G. Schalkwijk

Published in: Diabetologia | Issue 8/2015

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Abstract

Over the years, new research has elucidated the importance of the very fast formation of AGEs by the highly reactive methylglyoxal (MGO). It has become clear that MGO triggers maladaptive responses in vascular tissue. To counteract the deleterious effects of MGO, organisms have an enzymatic glyoxalase defence system in which MGO is converted to d-lactate, with glyoxalase 1 (GLO1) as the key enzyme in this system. Significant progress has been made towards the understanding of the MGO–GLO1 pathway in the pathogenesis of vascular disease in diabetes. This commentary highlights some lines of current research and future perspectives. The work conducted so far is only the starting point—in the coming 50 years, the MGO–GLO1 pathway will be the subject of intensified research, with special focus on pathophysiological pathways, the use of this system for early screening and risk prediction, and the development of intervention strategies for preventing vascular complications in people with and without diabetes. This is one of a series of commentaries under the banner ‘50 years forward’, giving personal opinions on future perspectives in diabetes, to celebrate the 50th anniversary of Diabetologia (1965–2015).
Literature
1.
go back to reference Guariguata L, Whiting DR, Hambleton I et al (2014) IDF Diabetes Atlas: global estimates of diabetes prevalence for 2013 and projections for 2035. Diabetes Res Clin Pract 103:137–149PubMedCrossRef Guariguata L, Whiting DR, Hambleton I et al (2014) IDF Diabetes Atlas: global estimates of diabetes prevalence for 2013 and projections for 2035. Diabetes Res Clin Pract 103:137–149PubMedCrossRef
2.
go back to reference Monnier VM, Cerami A (1981) Nonenzymatic browning in vivo: possible process for aging of long-lived proteins. Science 211:491–493PubMedCrossRef Monnier VM, Cerami A (1981) Nonenzymatic browning in vivo: possible process for aging of long-lived proteins. Science 211:491–493PubMedCrossRef
3.
go back to reference Shinohara M, Thornalley PJ, Giardino I et al (1998) Overexpression of glyoxalase-I in bovine endothelial cells inhibits intracellular advanced glycation endproduct formation and prevents hyperglycemia-induced increases in macromolecular endocytosis. J Clin Invest 101:1142–1147PubMedCentralPubMedCrossRef Shinohara M, Thornalley PJ, Giardino I et al (1998) Overexpression of glyoxalase-I in bovine endothelial cells inhibits intracellular advanced glycation endproduct formation and prevents hyperglycemia-induced increases in macromolecular endocytosis. J Clin Invest 101:1142–1147PubMedCentralPubMedCrossRef
4.
go back to reference Rabbani N, Thornalley PJ (2014) Measurement of methylglyoxal by stable isotopic dilution analysis LC-MS/MS with corroborative prediction in physiological samples. Nat Protoc 9:1969–1979 Rabbani N, Thornalley PJ (2014) Measurement of methylglyoxal by stable isotopic dilution analysis LC-MS/MS with corroborative prediction in physiological samples. Nat Protoc 9:1969–1979
5.
go back to reference Cavalot F, Pagliarino A, Valle M et al (2011) Postprandial blood glucose predicts cardiovascular events and all-cause mortality in type 2 diabetes in a 14-year follow-up: lessons from the San Luigi Gonzaga Diabetes Study. Diabetes Care 34:2237–2243PubMedCentralPubMedCrossRef Cavalot F, Pagliarino A, Valle M et al (2011) Postprandial blood glucose predicts cardiovascular events and all-cause mortality in type 2 diabetes in a 14-year follow-up: lessons from the San Luigi Gonzaga Diabetes Study. Diabetes Care 34:2237–2243PubMedCentralPubMedCrossRef
6.
go back to reference Maessen DE, Hanssen NM, Scheijen JL et al (2015) Post-glucose load plasma α-dicarbonyl concentrations are increased in individuals with impaired glucose metabolism and type 2 diabetes: The CODAM study. Diabetes Care 38:913–920 Maessen DE, Hanssen NM, Scheijen JL et al (2015) Post-glucose load plasma α-dicarbonyl concentrations are increased in individuals with impaired glucose metabolism and type 2 diabetes: The CODAM study. Diabetes Care 38:913–920
7.
go back to reference Hanssen NM, Beulens JW, van Dieren S et al (2015) Plasma advanced glycation end products are associated with incident cardiovascular events in individuals with type 2 diabetes: a case-cohort study with a median follow-up of 10 years (EPIC-NL). Diabetes 64:257–265PubMedCrossRef Hanssen NM, Beulens JW, van Dieren S et al (2015) Plasma advanced glycation end products are associated with incident cardiovascular events in individuals with type 2 diabetes: a case-cohort study with a median follow-up of 10 years (EPIC-NL). Diabetes 64:257–265PubMedCrossRef
8.
go back to reference Makinen VP, Civelek M, Meng Q et al (2014) Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. PLoS Genet 10: e1004502PubMedCentralPubMedCrossRef Makinen VP, Civelek M, Meng Q et al (2014) Integrative genomics reveals novel molecular pathways and gene networks for coronary artery disease. PLoS Genet 10: e1004502PubMedCentralPubMedCrossRef
9.
go back to reference Rabbani N, Thornalley PJ (2014) Dicarbonyl proteome and genome damage in metabolic and vascular disease. Biochem Soc Trans 42:425–432PubMedCrossRef Rabbani N, Thornalley PJ (2014) Dicarbonyl proteome and genome damage in metabolic and vascular disease. Biochem Soc Trans 42:425–432PubMedCrossRef
10.
go back to reference Hanssen NM, Wouters K, Huijberts MS et al (2014) Higher levels of advanced glycation endproducts in human carotid atherosclerotic plaques are associated with a rupture-prone phenotype. Eur Heart J 35:1137–1146PubMedCrossRef Hanssen NM, Wouters K, Huijberts MS et al (2014) Higher levels of advanced glycation endproducts in human carotid atherosclerotic plaques are associated with a rupture-prone phenotype. Eur Heart J 35:1137–1146PubMedCrossRef
11.
go back to reference Morcos M, Du X, Pfisterer F, Hutter H et al (2008) Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegans. Aging Cell 7:260–269PubMedCrossRef Morcos M, Du X, Pfisterer F, Hutter H et al (2008) Glyoxalase-1 prevents mitochondrial protein modification and enhances lifespan in Caenorhabditis elegans. Aging Cell 7:260–269PubMedCrossRef
12.
go back to reference Xue J, Ray R, Singer D et al (2014) The receptor for advanced glycation end products (RAGE) specifically recognizes methylglyoxal-derived AGEs. Biochemistry 53:3327–3335PubMedCentralPubMedCrossRef Xue J, Ray R, Singer D et al (2014) The receptor for advanced glycation end products (RAGE) specifically recognizes methylglyoxal-derived AGEs. Biochemistry 53:3327–3335PubMedCentralPubMedCrossRef
13.
go back to reference El-Osta A, Brasacchio D, Yao D et al (2008) Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia. J Exp Med 205:2409–2417PubMedCentralPubMedCrossRef El-Osta A, Brasacchio D, Yao D et al (2008) Transient high glucose causes persistent epigenetic changes and altered gene expression during subsequent normoglycemia. J Exp Med 205:2409–2417PubMedCentralPubMedCrossRef
14.
go back to reference Bierhaus A, Fleming T, Stoyanov S et al (2012) Methylglyoxal modification of Nav1.8 facilitates nociceptive neuron firing and causes hyperalgesia in diabetic neuropathy. Nat Med 18:926–933PubMedCrossRef Bierhaus A, Fleming T, Stoyanov S et al (2012) Methylglyoxal modification of Nav1.8 facilitates nociceptive neuron firing and causes hyperalgesia in diabetic neuropathy. Nat Med 18:926–933PubMedCrossRef
15.
go back to reference Xue M, Rabbani N, Momiji H et al (2012) Transcriptional control of glyoxalase 1 by Nrf2 provides a stress-responsive defence against dicarbonyl glycation. Biochem J 443:213–222PubMedCrossRef Xue M, Rabbani N, Momiji H et al (2012) Transcriptional control of glyoxalase 1 by Nrf2 provides a stress-responsive defence against dicarbonyl glycation. Biochem J 443:213–222PubMedCrossRef
Metadata
Title
Vascular AGE-ing by methylglyoxal: the past, the present and the future
Author
Casper G. Schalkwijk
Publication date
01-08-2015
Publisher
Springer Berlin Heidelberg
Published in
Diabetologia / Issue 8/2015
Print ISSN: 0012-186X
Electronic ISSN: 1432-0428
DOI
https://doi.org/10.1007/s00125-015-3597-5

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