Leptin Receptor-Deficient Mice Show Significant Heterogeneity in Response to High Non-heme Iron Diet.

Recent studies have shown an association between iron homeostasis, obesity and diabetes. In this work, we investigated the differences in the metabolic status and inflammation in liver, pancreas and visceral adipose tissue of leptin receptor-deficient mice dependent on high iron concentration diet. 3-month-old male BKS-Leprdb/db/JOrlRj () mice were divided into two groups, which were fed with different diets containing high iron (29 g/kg, = 57) or standard iron (0.178 g/kg; = 42) concentrations for 4 months. As anticipated, standard iron-fed mice developed obesity and diabetes. However, high iron-fed mice exhibited a wide heterogeneity. By dividing into two subgroups at the diabetes level, non-diabetic subgroup 1 (<13.5 mmol/l, = 30) significantly differed from diabetic subgroup two (>13.5 mmol/l, = 27). Blood glucose concentration, HbA1c value, inflammation markers interleukin six and tumor necrosis factor α and heme oxygenase one in visceral adipose tissue were reduced in subgroup one compared to subgroup two. In contrast, body weight, C-peptide, serum insulin and serum iron concentrations, pancreatic islet and signal ratio as well as cholesterol, LDL and HDL levels were enhanced in subgroup one. While these significant differences require further studies and explanation, our results might also explain the often-contradictory results of the metabolic studies with mice.