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Advanced Glycation and Lipoxidation End Products–Amplifiers of Inflammation: The Role of Food

From UCL Institute of Hepatology, University College, London Medical School, London, United Kingdom

Correspondence: Stig Bengmark, MD, PhD, FRACS (hon), FRCPS (hon), 185 Barrier Point Road, Royal Docks, London, E16 2SE, United Kingdom. Electronic mail may be sent to s.bengmark{at}ucl.ac.uk.

Background: High levels of glycated and lipoxidated proteins and peptides in the body are repeatedly associated with chronic diseases. These molecules are strongly associated with activation of a specific receptor called RAGE and a long-lasting exaggerated level of inflammation in the body. Methods: PubMed reports over 5000 papers plus >13,500 articles about the related HbA_1c, most of them published in the past 5 years. Most of the available abstracts have been read and approximately 800 full papers have been studied. Results: RAGE, a member of the immunoglobulin superfamily of cell surface molecules and receptor for advanced glycation end products, known since 1992, functions as a master switch, induces sustained activation of nuclear factor B (NFB), suppresses a series of endogenous autoregulatory functions, and converts long-lasting proinflammatory signals into sustained cellular dysfunction and disease. Its activation is associated with high levels of dysfunctioning proteins in body fluids and tissues, and is strongly associated with a series of diseases from allergy and Alzheimers to rheumatoid arthritis and urogenital disorders. Heat treatment, irradiation, and ionization of foods increase the content of dysfunctioning molecules. Conclusions: More than half of the studies are performed in diabetes and chronic renal diseases; there are few studies in other diseases. Most of our knowledge is based on animal studies and in vitro studies. These effects are worth further exploration both experimentally and clinically. An avoidance of foods rich in deranged proteins and peptides, and the consumption of antioxidants, especially polyphenols, seem to counteract such a development.

Journal of Parenteral and Enteral Nutrition, Vol. 31, No. 5, 430-440 (2007)
DOI: 10.1177/0148607107031005430


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