Carnosinase-1 overexpression, but not aerobic exercise training, affects the development of diabetic nephropathy in BTBR ob/ob mice

• Published in: American journal of physiology. Renal physiology 2020-04, Vol.318 (4), p.F1030-F1040
• Main Authors: Everaert, Inge, He, Junling, Hanssens, Maxime, Stautemas, Jan, Bakker, Kim, Albrecht, Thomas, Zhang, Shiqi, Van der Stede, Thibaux, Vanhove, Kenneth, Hoetker, David, Howsam, Michael, Tessier, Frédéric J, Yard, Benito, Baba, Shahid P, Baelde, Hans J, Derave, Wim
• Format: Article
• Language: English
• Subjects: Aerobics; Animal models; Developmental stages; Diabetes; Diabetes mellitus; Enzymes; Exercise; Fitness training programs; Histidine; Hyperlipidemia; Hypertrophy; Ion channels (cyclic nucleotide-gated); Kidneys; Life Sciences; Nephropathy; Physical fitness; Physical training
• ISSN: 1931-857X; 1522-1466
• DOI: 10.1152/ajprenal.00329.2019

Manipulation of circulating histidine-containing dipeptides (HCD) has been shown to affect the development of diabetes and early-stage diabetic nephropathy (DN). The aim of the present study was to investigate whether such interventions, which potentially alter levels of circulating HCD, also affect the development of advanced-stage DN. Two interventions, aerobic exercise training and overexpression of the human carnosinase-1 (hCN1) enzyme, were tested. BTBR mice were either subjected to aerobic exercise training (20 wk) or genetically manipulated to overexpress hCN1, and different diabetes- and DN-related markers were compared with control and healthy (wild-type) mice. An acute exercise study was performed to elucidate the effect of obesity, acute running, and hCN1 overexpression on plasma HCD levels. Chronic aerobic exercise training did not affect the development of diabetes or DN, but hCN1 overexpression accelerated hyperlipidemia and aggravated the development of albuminuria, mesangial matrix expansion, and glomerular hypertrophy of mice. In line, plasma, kidney, and muscle HCD were markedly lower in versus wild-type mice, and plasma and kidney HCD in particular were lower in hCN1 versus mice but were unaffected by aerobic exercise. In conclusion, advanced glomerular damage is accelerated in mice overexpressing the hCN1 enzyme but not protected by chronic exercise training. Interestingly, we showed, for the first time, that the development of DN is closely linked to renal HCD availability. Further research will have to elucidate whether the stimulation of renal HCD levels can be a therapeutic strategy to reduce the risk for developing DN.