Literature DB >> 28515343

Kidney, heart and brain: three organs targeted by ageing and glycation.

Marie Frimat1,2, Maité Daroux3,4, Rachel Litke3,5, Rémi Nevière3,6, Frédéric J Tessier3, Eric Boulanger1,5.   

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.
© 2017 The Author(s). published by Portland Press Limited on behalf of the Biochemical Society.

Entities:  

Keywords:  advanced glycation end-products; ageing; chronic kidney disease; cognitive decline; heart dysfunction

Mesh:

Substances:

Year:  2017        PMID: 28515343     DOI: 10.1042/CS20160823

Source DB:  PubMed          Journal:  Clin Sci (Lond)        ISSN: 0143-5221            Impact factor:   6.124


  21 in total

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Review 4.  Carbotoxicity-Noxious Effects of Carbohydrates.

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5.  Adiponectin inhibits D‑gal‑induced cardiomyocyte senescence via AdipoR1/APPL1.

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Review 7.  Probing Protein Glycation by Chromatography and Mass Spectrometry: Analysis of Glycation Adducts.

Authors:  Alena Soboleva; Maria Vikhnina; Tatiana Grishina; Andrej Frolov
Journal:  Int J Mol Sci       Date:  2017-11-28       Impact factor: 5.923

Review 8.  Effects of d-galactose-induced ageing on the heart and its potential interventions.

Authors:  Cherry Bo-Htay; Siripong Palee; Nattayaporn Apaijai; Siriporn C Chattipakorn; Nipon Chattipakorn
Journal:  J Cell Mol Med       Date:  2018-01-24       Impact factor: 5.310

9.  Thymoquinone and Curcumin Defeat Aging-Associated Oxidative Alterations Induced by D-Galactose in Rats' Brain and Heart.

Authors:  Ali H El-Far; Yaser H A Elewa; Elsayeda-Zeinab A Abdelfattah; Abdel-Wahab A Alsenosy; Mustafa S Atta; Khalid M Abou-Zeid; Soad K Al Jaouni; Shaker A Mousa; Ahmed E Noreldin
Journal:  Int J Mol Sci       Date:  2021-06-25       Impact factor: 5.923

10.  l-Theanine Ameliorates d-Galactose-Induced Brain Damage in Rats via Inhibiting AGE Formation and Regulating Sirtuin1 and BDNF Signaling Pathways.

Authors:  Li Zeng; Ling Lin; Ling Chen; Wenjun Xiao; Zhihua Gong
Journal:  Oxid Med Cell Longev       Date:  2021-07-19       Impact factor: 6.543

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