TY - JOUR
T1 - Age and Diet Modulate the Insulin-Sensitizing Effects of Exercise
T2 - A Tracer-Based Oral Glucose Tolerance Test
AU - Vieira-Lara, Marcel A.
AU - Reijne, Aaffien C.
AU - Koshian, Serj
AU - Ciapaite, Jolita
AU - Abegaz, Fentaw
AU - Talarovicova, Alzbeta
AU - van Dijk, Theo H.
AU - Versloot, Christian J.
AU - Bandsma, Robert H. J.
AU - Wolters, Justina C.
AU - Groen, Albert K.
AU - Reijngoud, Dirk-Jan
AU - van Dijk, Gertjan
AU - Bakker, Barbara M.
N1 - Funding Information:
Acknowledgments. We thank Maaike Oosterveer and Angela Tol of the Laboratory of Pediatrics of the University Medical Center Groningen for valuable discussions. Funding. This study was funded by a grant from the Netherlands Organization for Scientific Research (NWO; grant 853.00.110), by DSM Nutritional products in the framework of the Complexity program (grant 645.001.001/ 3501), a University Medical Center Groningen (UMCG) MD/PhD fellowship to C.J.V., and a UMCG–Graduate School of Medical Sciences PhD fellowship to M.A.V.-L.
Publisher Copyright:
© 2023 by the American Diabetes Association.
PY - 2023/7/1
Y1 - 2023/7/1
N2 - Diet modulates the development of insulin resistance during aging. This includes tissue-specific alterations in insulin signaling and mitochondrial function, which ultimately affect glucose homeostasis. Exercise stimulates glucose clearance and mitochondrial lipid oxidation and also enhances insulin sensitivity (IS). It is not well known how exercise interacts with age and diet in the development of insulin resistance. To investigate this, oral glucose tolerance tests with tracers were conducted in mice ranging from 4 to 21 months of age, fed a low-fat diet (LFD) or high-fat diet (HFD) with or without life-long voluntary access to a running wheel (RW). We developed a computational model to derive glucose fluxes, which were commensurate with inde-pendent values from steady-state tracer infusions. Values for an IS index derived for peripheral tissues (IS-P) and one for the liver (IS-L) were steeply decreased by aging and an HFD. This preceded the age-dependent decline in the mitochondrial capacity to oxidize lipids. In young animals fed an LFD, RW access enhanced the IS-P concomitantly with the muscle β-oxidation capac-ity. Surprisingly, RW access completely prevented the age-dependent IS-L decrease; however this only oc-curred in animals fed an LFD. Therefore, this study in-dicates that endurance exercise can improve the age-dependent decline in organ-specific ISifpairedwitha healthy diet.
AB - Diet modulates the development of insulin resistance during aging. This includes tissue-specific alterations in insulin signaling and mitochondrial function, which ultimately affect glucose homeostasis. Exercise stimulates glucose clearance and mitochondrial lipid oxidation and also enhances insulin sensitivity (IS). It is not well known how exercise interacts with age and diet in the development of insulin resistance. To investigate this, oral glucose tolerance tests with tracers were conducted in mice ranging from 4 to 21 months of age, fed a low-fat diet (LFD) or high-fat diet (HFD) with or without life-long voluntary access to a running wheel (RW). We developed a computational model to derive glucose fluxes, which were commensurate with inde-pendent values from steady-state tracer infusions. Values for an IS index derived for peripheral tissues (IS-P) and one for the liver (IS-L) were steeply decreased by aging and an HFD. This preceded the age-dependent decline in the mitochondrial capacity to oxidize lipids. In young animals fed an LFD, RW access enhanced the IS-P concomitantly with the muscle β-oxidation capac-ity. Surprisingly, RW access completely prevented the age-dependent IS-L decrease; however this only oc-curred in animals fed an LFD. Therefore, this study in-dicates that endurance exercise can improve the age-dependent decline in organ-specific ISifpairedwitha healthy diet.
UR - https://www.scopus.com/pages/publications/85163678661
U2 - 10.2337/db22-0746
DO - 10.2337/db22-0746
M3 - Article
C2 - 37094362
SN - 0012-1797
VL - 72
SP - 872
EP - 883
JO - Diabetes
JF - Diabetes
IS - 7
ER -