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Published on: October 12, 2017
Molecular strategies to prevent, inhibit, and degrade advanced glycoxidation and advanced lipoxidation end products
Giancarlo Aldini1, Giulio Vistoli, Milan Stefek
1Department of Pharmaceutical Sciences, University of Milan, Milan, Italy.
Abstract:
The advanced glycoxidation end products (AGEs) and lipoxidation end products (ALEs) contribute to the development of diabetic complications and of other pathologies. The review discusses the possibilities of counteracting the formation and stimulating the degradation of these species by pharmaceuticals and natural compounds. The review discusses inhibitors of ALE and AGE formation, cross-link breakers, ALE/AGE elimination by enzymes and proteolytic systems, receptors for advanced glycation end products (RAGEs) and blockade of the ligand-RAGE axis.
Insights
Advanced glycoxidation and lipoxidation end products (AGEs and ALEs) drive diabetic complications. This review explores pharmaceuticals and natural compounds to inhibit their formation and enhance their degradation, offering therapeutic strategies.
Area of Science:
- Biochemistry
- Pathology
- Pharmacology
Background:
- Advanced glycoxidation end products (AGEs) and lipoxidation end products (ALEs) are implicated in diabetic complications and other diseases.
- Their accumulation results from metabolic dysregulation and oxidative stress.
Purpose of the Study:
- To review current strategies for counteracting AGEs and ALEs.
- To explore therapeutic interventions targeting the formation and degradation of these compounds.
Main Methods:
- Literature review of pharmaceuticals and natural compounds.
- Analysis of mechanisms targeting AGE/ALE formation, degradation, and signaling.
Main Results:
- Identified inhibitors of AGE and ALE formation.
- Discussed cross-link breakers and enzymatic/proteolytic degradation pathways.
- Examined the role of the receptor for advanced glycation end products (RAGE) and its blockade.
Conclusions:
- Pharmaceuticals and natural compounds offer potential for managing AGEs and ALEs.
- Targeting RAGE and its ligands presents a promising therapeutic avenue.
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