Association of four differently processed diets with plasma and urine advanced glycation end products and serum soluble receptor for advanced glycation end products concentration in healthy dogs

Advanced glycation end products (AGEs), formed via the Maillard reaction (MR) during processing of foods, have been implicated in inflammatory and degenerative diseases in human beings. Cellular damage is primarily caused by AGE binding with the receptor for AGEs (RAGE) on cell membranes. An isoform...

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Veröffentlicht in:Journal of animal physiology and animal nutrition 2024-05, Vol.108 (3), p.735-751
Hauptverfasser: Bridglalsingh, Siobhan, Archer‐Hartmann, Stephanie, Azadi, Parastoo, Barbier de La Serre, Claire, Remillard, Rebecca L., Sunvold, Gregory D., Bartges, Joseph W.
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Sprache:eng
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Zusammenfassung:Advanced glycation end products (AGEs), formed via the Maillard reaction (MR) during processing of foods, have been implicated in inflammatory and degenerative diseases in human beings. Cellular damage is primarily caused by AGE binding with the receptor for AGEs (RAGE) on cell membranes. An isoform of RAGE, soluble RAGE (sRAGE), acts as a decoy receptor binding circulating AGEs preventing cellular activation. Pet food manufacturing involves processing methods similar to human food processing that may increase dietary AGEs (dAGEs). We hypothesized that diet, plasma and urine AGEs, and serum sRAGE concentrations would differ between thermally processed diets. This study examined the association of four differently processed diets: ultra‐processed canned wet food (WF); ultra‐processed dry food (DF); moderately processed air‐dried food (ADF) and minimally processed mildly cooked food (MF) on total plasma levels of the AGEs, carboxymethyllysine (CML), carboxyethyllysine (CEL), methylglyoxal hydroimidazolone‐1, glyoxal hydroimidazolone‐1, argpyrimidine, urine CML, CEL and lysinoalanine, and serum sRAGE concentration. Ultra‐high‐performance liquid chromatography–tandem mass spectrometry was used to measure AGEs. sRAGE concentration was measured using a commercial canine‐specific enzyme‐linked immunosorbent assay kit. Total dAGEs (mg/100 kcal as fed) were higher in WF than in other diets. Plasma total AGEs (nM/50 μL) were significantly higher with WF, with no difference found between DF, ADF, and MF; however, ADF was significantly higher than MF. Urine CML (nmol AGEs/mmol creatinine) was significantly higher with DF than with WF and MF. There were no significant differences in total urine AGEs or serum sRAGE concentration between diets. In conclusion, different methods of processing pet foods are associated with varied quantities of AGEs influencing total plasma AGE concentration in healthy dogs. Serum sRAGE concentration did not vary across diets but differences in total AGE/sRAGE ratio were observed between MF and WF and, ADF and DF.
ISSN:0931-2439
1439-0396
1439-0396
DOI:10.1111/jpn.13927