Kidney, heart and brain: three organs targeted by ageing and glycation
Marie Frimat1,2, Maité Daroux3,4, Rachel Litke3,5
1University of Lille, INSERM, CHU Lille, U995-LIRIC-Lille Inflammation Research International Centre, F-59000 Lille, France marie.frimat@chru-lille.fr eric.boulanger@univ-lille2.fr.
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.
Insights
Advanced glycation end-products (AGEs) contribute to aging and chronic diseases by modifying proteins and activating inflammatory pathways. Preventing AGE accumulation may be a therapeutic strategy for healthy aging, though causal links require further validation.
Area of Science:
- Biochemistry
- Pathology
- Gerontology
Background:
- Advanced glycation end-products (AGEs) form from non-enzymatic reactions between sugars and proteins.
- AGE accumulation is implicated in chronic hyperglycemia and age-related diseases.
- AGEs can accelerate aging via protein modification and inflammatory signaling.
Purpose of the Study:
- To review the pathogenic role of AGEs in age-related diseases.
- To focus on AGEs' impact on the kidney, heart, and brain.
- To explore the therapeutic potential of preventing AGE accumulation for successful aging.
Main Methods:
- Literature review of current knowledge on AGEs.
- Focus on age-related diseases: chronic kidney disease, heart dysfunction, neurodegenerative diseases.
- Analysis of evidence from animal and epidemiological studies.
Main Results:
- AGEs are linked to protein modifications and inflammation, potentially accelerating aging.
- Strong associations exist between glycation and age-related pathogenesis in target organs.
- Causal links between AGEs and specific diseases require further validation.
Conclusions:
- AGEs play a significant role in the pathogenesis of age-related diseases.
- Preventing AGE accumulation is a potential therapeutic avenue for healthy aging.
- Further research is needed to confirm causal relationships and validate anti-AGE strategies.
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