Title | Mechanism by Which Caloric Restriction Improves Insulin Sensitivity in Sedentary Obese Adults. |
Publication Type | Journal Article |
Year of Publication | 2016 |
Authors | Johnson, ML, Distelmaier, K, Lanza, IR, Irving, BA, Robinson, MM, Konopka, AR, Shulman, GI, K Nair, S |
Journal | Diabetes |
Volume | 65 |
Issue | 1 |
Pagination | 74-84 |
Date Published | 2016 Jan |
ISSN | 1939-327X |
Keywords | Amino Acids, Blood Glucose, Blotting, Western, Caloric Restriction, Calorimetry, Indirect, Carrier Proteins, Case-Control Studies, Ceramides, Diglycerides, Energy Metabolism, Female, Glucose Clamp Technique, Humans, Hydrogen Peroxide, Insulin Resistance, Male, Middle Aged, Mitochondria, Muscle, Muscle, Skeletal, Obesity, Oxidation-Reduction, Sedentary Lifestyle |
Abstract | Caloric restriction (CR) improves insulin sensitivity and reduces the incidence of diabetes in obese individuals. The underlying mechanisms whereby CR improves insulin sensitivity are not clear. We evaluated the effect of 16 weeks of CR on whole-body insulin sensitivity by pancreatic clamp before and after CR in 11 obese participants (BMI = 35 kg/m(2)) compared with 9 matched control subjects (BMI = 34 kg/m(2)). Compared with the control subjects, CR increased the glucose infusion rate needed to maintain euglycemia during hyperinsulinemia, indicating enhancement of peripheral insulin sensitivity. This improvement in insulin sensitivity was not accompanied by changes in skeletal muscle mitochondrial oxidative capacity or oxidant emissions, nor were there changes in skeletal muscle ceramide, diacylglycerol, or amino acid metabolite levels. However, CR lowered insulin-stimulated thioredoxin-interacting protein (TXNIP) levels and enhanced nonoxidative glucose disposal. These results support a role for TXNIP in mediating the improvement in peripheral insulin sensitivity after CR. |
DOI | 10.2337/db15-0675 |
Alternate Journal | Diabetes |
PubMed ID | 26324180 |
PubMed Central ID | PMC4686951 |
Grant List | R01 DK049230 / DK / NIDDK NIH HHS / United States R01 DK041973 / DK / NIDDK NIH HHS / United States R01 DK059615 / DK / NIDDK NIH HHS / United States UL1-TR-000135 / TR / NCATS NIH HHS / United States T32-DK-007352 / DK / NIDDK NIH HHS / United States R24-DK-090963 / DK / NIDDK NIH HHS / United States T32 DK007198 / DK / NIDDK NIH HHS / United States R24 DK090963 / DK / NIDDK NIH HHS / United States P30 DK050456 / DK / NIDDK NIH HHS / United States DK-50456 / DK / NIDDK NIH HHS / United States KL2 TR000136 / TR / NCATS NIH HHS / United States KL2 RR024151 / RR / NCRR NIH HHS / United States U24 DK100469 / DK / NIDDK NIH HHS / United States R01-DK-41973 / DK / NIDDK NIH HHS / United States T32-DK-007198 / DK / NIDDK NIH HHS / United States UL1 TR000135 / TR / NCATS NIH HHS / United States / / Howard Hughes Medical Institute / United States R01-DK-49230 / DK / NIDDK NIH HHS / United States T32 DK007352 / DK / NIDDK NIH HHS / United States KL2-RR-024151 / RR / NCRR NIH HHS / United States U24-DK-100469 / DK / NIDDK NIH HHS / United States KL2-TR-000136-07 / TR / NCATS NIH HHS / United States R56 DK041973 / DK / NIDDK NIH HHS / United States |