The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy

The glyoxalase system is critical for the detoxification of advanced glycation end-products (AGEs). AGEs are toxic compounds resulting from the non-enzymatic modification of biomolecules by sugars or their metabolites through a process called glycation. AGEs have adverse effects on many tissues, pla...

Full description

Bibliographic Details
Main Authors: Gemma Aragonès, Sheldon Rowan, Sarah G. Francisco, Elizabeth A. Whitcomb, Wenxin Yang, Giuliana Perini-Villanueva, Casper G. Schalkwijk, Allen Taylor, Eloy Bejarano
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/10/8/1852
id doaj-4952ec86a10c4e1eb7a448087ba35769
record_format Article
spelling doaj-4952ec86a10c4e1eb7a448087ba357692021-08-26T13:36:51ZengMDPI AGCells2073-44092021-07-01101852185210.3390/cells10081852The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing StrategyGemma Aragonès0Sheldon Rowan1Sarah G. Francisco2Elizabeth A. Whitcomb3Wenxin Yang4Giuliana Perini-Villanueva5Casper G. Schalkwijk6Allen Taylor7Eloy Bejarano8Laboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USADepartment of Internal Medicine, CARIM School for Cardiovascular Diseases, Maastricht University Medical Centre, 6200 MD Maastricht, The NetherlandsLaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USALaboratory for Nutrition and Vision Research, USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02155, USAThe glyoxalase system is critical for the detoxification of advanced glycation end-products (AGEs). AGEs are toxic compounds resulting from the non-enzymatic modification of biomolecules by sugars or their metabolites through a process called glycation. AGEs have adverse effects on many tissues, playing a pathogenic role in the progression of molecular and cellular aging. Due to the age-related decline in different anti-AGE mechanisms, including detoxifying mechanisms and proteolytic capacities, glycated biomolecules are accumulated during normal aging in our body in a tissue-dependent manner. Viewed in this way, anti-AGE detoxifying systems are proposed as therapeutic targets to fight pathological dysfunction associated with AGE accumulation and cytotoxicity. Here, we summarize the current state of knowledge related to the protective mechanisms against glycative stress, with a special emphasis on the glyoxalase system as the primary mechanism for detoxifying the reactive intermediates of glycation. This review focuses on glyoxalase 1 (GLO1), the first enzyme of the glyoxalase system, and the rate-limiting enzyme of this catalytic process. Although GLO1 is ubiquitously expressed, protein levels and activities are regulated in a tissue-dependent manner. We provide a comparative analysis of GLO1 protein in different tissues. Our findings indicate a role for the glyoxalase system in homeostasis in the eye retina, a highly oxygenated tissue with rapid protein turnover. We also describe modulation of the glyoxalase system as a therapeutic target to delay the development of age-related diseases and summarize the literature that describes the current knowledge about nutritional compounds with properties to modulate the glyoxalase system.https://www.mdpi.com/2073-4409/10/8/1852glycative stressglyoxalase systemagingproteotoxicity
collection DOAJ
language English
format Article
sources DOAJ
author Gemma Aragonès
Sheldon Rowan
Sarah G. Francisco
Elizabeth A. Whitcomb
Wenxin Yang
Giuliana Perini-Villanueva
Casper G. Schalkwijk
Allen Taylor
Eloy Bejarano
spellingShingle Gemma Aragonès
Sheldon Rowan
Sarah G. Francisco
Elizabeth A. Whitcomb
Wenxin Yang
Giuliana Perini-Villanueva
Casper G. Schalkwijk
Allen Taylor
Eloy Bejarano
The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
Cells
glycative stress
glyoxalase system
aging
proteotoxicity
author_facet Gemma Aragonès
Sheldon Rowan
Sarah G. Francisco
Elizabeth A. Whitcomb
Wenxin Yang
Giuliana Perini-Villanueva
Casper G. Schalkwijk
Allen Taylor
Eloy Bejarano
author_sort Gemma Aragonès
title The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
title_short The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
title_full The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
title_fullStr The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
title_full_unstemmed The Glyoxalase System in Age-Related Diseases: Nutritional Intervention as Anti-Ageing Strategy
title_sort glyoxalase system in age-related diseases: nutritional intervention as anti-ageing strategy
publisher MDPI AG
series Cells
issn 2073-4409
publishDate 2021-07-01
description The glyoxalase system is critical for the detoxification of advanced glycation end-products (AGEs). AGEs are toxic compounds resulting from the non-enzymatic modification of biomolecules by sugars or their metabolites through a process called glycation. AGEs have adverse effects on many tissues, playing a pathogenic role in the progression of molecular and cellular aging. Due to the age-related decline in different anti-AGE mechanisms, including detoxifying mechanisms and proteolytic capacities, glycated biomolecules are accumulated during normal aging in our body in a tissue-dependent manner. Viewed in this way, anti-AGE detoxifying systems are proposed as therapeutic targets to fight pathological dysfunction associated with AGE accumulation and cytotoxicity. Here, we summarize the current state of knowledge related to the protective mechanisms against glycative stress, with a special emphasis on the glyoxalase system as the primary mechanism for detoxifying the reactive intermediates of glycation. This review focuses on glyoxalase 1 (GLO1), the first enzyme of the glyoxalase system, and the rate-limiting enzyme of this catalytic process. Although GLO1 is ubiquitously expressed, protein levels and activities are regulated in a tissue-dependent manner. We provide a comparative analysis of GLO1 protein in different tissues. Our findings indicate a role for the glyoxalase system in homeostasis in the eye retina, a highly oxygenated tissue with rapid protein turnover. We also describe modulation of the glyoxalase system as a therapeutic target to delay the development of age-related diseases and summarize the literature that describes the current knowledge about nutritional compounds with properties to modulate the glyoxalase system.
topic glycative stress
glyoxalase system
aging
proteotoxicity
url https://www.mdpi.com/2073-4409/10/8/1852
work_keys_str_mv AT gemmaaragones theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT sheldonrowan theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT sarahgfrancisco theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT elizabethawhitcomb theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT wenxinyang theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT giulianaperinivillanueva theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT caspergschalkwijk theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT allentaylor theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT eloybejarano theglyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT gemmaaragones glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT sheldonrowan glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT sarahgfrancisco glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT elizabethawhitcomb glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT wenxinyang glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT giulianaperinivillanueva glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT caspergschalkwijk glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT allentaylor glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
AT eloybejarano glyoxalasesysteminagerelateddiseasesnutritionalinterventionasantiageingstrategy
_version_ 1721194356825653248