Short-term effects of dietary advanced glycation end products in rats

Abstract

Dietary advanced glycation end products (AGE) formed during heating of food have gained interest as potential nutritional toxins with adverse effects on inflammation and glucose metabolism. In the present study, we investigated the short-term effects of high and low molecular weight (HMW and LMW) dietary AGE on insulin sensitivity, expression of the receptor for AGE (RAGE), the AGE receptor 1 (AGER1) and TNF-α, F2-isoprostaglandins, body composition and food intake. For 2 weeks, thirty-six Sprague-Dawley rats were fed a diet containing 20% milk powder with different proportions of this being given as heated milk powder (0, 40 or 100%), either native (HMW) or hydrolysed (LMW). Gene expression of RAGE and AGER1 in whole blood increased in the group receiving a high AGE LMW diet, which also had the highest urinary excretion of the AGE, methylglyoxal-derived hydroimidazolone 1 (MG-H1). Urinary excretion of N ε-carboxymethyl-lysine increased with increasing proportion of heat-treated milk powder in the HMW and LMW diets but was unrelated to gene expression. There was no difference in insulin sensitivity, F2-isoprostaglandins, food intake, water intake, body weight or body composition between the groups. In conclusion, RAGE and AGER1 expression can be influenced by a high AGE diet after only 2 weeks in proportion to MG-H1 excretion. No other short-term effects were observed.

Keywords: AGE advanced glycation end products; AGER1 gene for advanced glycation end product receptor 1; Advanced glycation end products; Body composition; CEL Nε -carboxyethyl-lysine; CML Nε -carboxymethyl-lysine; Gene expression; Gene for advanced glycation end product receptor 1; Gene for receptor for advanced glycation end products; H-AGE high advanced glycation end product; HMW high molecular weight; Insulin sensitivity; L-AGE low advanced glycation end product; LMW low molecular weight; MG-H1 methylglyoxal-derived hydroimidazolone-1; RAGE gene for receptor for advanced glycation end products; Rats.