Kidney, heart and brain: three organs targeted by ageing and glycation
Abstract
Advanced glycation end-product (AGE) is the generic term for a heterogeneous group of derivatives arising from a non-enzymatic reaction between reducing sugars and proteins. In recent years, evidence has accumulated that incriminates AGEs in pathogenic processes associated with both chronic hyperglycaemia and age-related diseases. Regardless of their exogenous or endogenous origin, the accumulation of AGEs and their derivatives could promote accelerated ageing by leading to protein modifications and activating several inflammatory signalling pathways via AGE-specific receptors. However, it remains to be demonstrated whether preventing the accumulation of AGEs and their effects is an important therapeutic option for successful ageing. The present review gives an overview of the current knowledge on the pathogenic role of AGEs by focusing on three AGE target organs: kidney, heart and brain. For each of these organs we concentrate on an age-related disease, each of which is a major public health issue: chronic kidney disease, heart dysfunction and neurodegenerative diseases. Even though strong connections have been highlighted between glycation and age-related pathogenesis, causal links still need to be validated. In each case, we report evidence and uncertainties suggested by animal or epidemiological studies on the possible link between pathogenesis and glycation in a chronic hyperglycaemic state, in the absence of diabetes, and with exogenous AGEs alone. Finally, we present some promising anti-AGE strategies that are currently being studied.
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AGEs can be produced in renal mesangial cells and induce expression of MCP-1.
“In addition, AGEs can be produced in renal mesangial cells and induce the expression of monocyte chemoattractant protein-1 (MCP-1).”
From Advanced glycation end products (AGEs) and other adducts in aging-related diseases and alcohol-mediated tissue injury (2021) · cites this paper as [70]
AGEs activate NF-κB, MAPK, and PKC to promote mesangial proliferative inhibition, hypertrophy, and apoptosis.
“AGEs also activate NF-κB, MAPK, and protein kinase C (PKC) to promote mesangial proliferative inhibition, hypertrophy, and apoptosis70,71.”
From Advanced glycation end products (AGEs) and other adducts in aging-related diseases and alcohol-mediated tissue injury (2021) · cites this paper as [70]
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References 250 · Cited by 88
- Authors
- Frimat, M., Daroux, M., Litke, R., Nevière, R., Tessier, F. J., & Boulanger, E.
- Affiliations
- Inserm (FR)
- University of Lille, INSERM, CHU Lille, U995–LIRIC–Lille Inflammation Research International Centre, F-59000 Lille, France
- Corresponding author
- Frimat, Marie
- Venue
- Clinical Science
- Publisher
- Portland Press Ltd.
- Published
- 2017-05-17
- Volume
- 131
- Issue
- 11
- Pages
- 1069-1092
- ISSN
- 0143-5221 (ISSN-L)
- 1470-8736
- OpenAlex
- W2614693007
- Cited by
- 88
- References
- 250
- Citations by year
- 2026: 5 · 2025: 5 · 2024: 7 · 2023: 9 · 2022: 9 · 2021: 13 · 2020: 10 · 2019: 15 · 2018: 12 · 2017: 3
- FWCI
- 1.47
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Science (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Advanced Glycation End Products research
- Health Sciences › Medicine › Nephrology › Chronic Kidney Disease and Diabetes
- Life Sciences › Agricultural and Biological Sciences › Food Science › Potato Plant Research
- Keywords
- advanced glycation end products, glycation, aging, chronic hyperglycemia, chronic kidney disease, cardiac dysfunction, neurodegenerative diseases, AGE receptor, inflammation, protein modification
- MeSH terms
- Receptor for Advanced Glycation End Products, Aging, Diet, Glycosylation, Heart Diseases, Humans, Glycation End Products, Advanced, Neurodegenerative Diseases, Renal Insufficiency, Chronic, Molecular Targeted Therapy
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