The naturally occurring dipeptide carnosine (
β-alanyl-L-histidine) is found in surprisingly large amounts in long-lived tissues and can delay ageing in cultured human fibroblasts.
Carnosine has been regarded largely as an anti-oxidant and free radical scavenger. More recently, an anti-glycating potential
has been discovered whereby carnosine can react with low-molecular-weight compounds that bear carbonyl groups (aldehydes and
ketones). Carbonyl groups, arising mostly from the attack of reactive oxygen species and ow-molecular-weight aldehydes and
ketones, accumulate on proteins during ageing. Here we propose, with supporting evidence, that carnosine can react with protein
carbonyl groups to produce protein-carbonyl-carnosine adducts (‘carnosinylated’ proteins). The various possible cellular fates
of the carnosinylated proteins are discussed. These proposals may help explain anti-ageing actions of carnosine and its presence
in non-mitotic cells of long-lived mammals.
Key words. Protein; aging; ageing; carbonyl; glycation; proteolysis; lipofuscin; advanced glycosylation end-product.
Received 29 November 1999; accepted 27 December 1999