4.6 Article

Dietary Selenium Requirement for the Prevention of Glucose Intolerance and Insulin Resistance in Middle-Aged Mice

期刊

JOURNAL OF NUTRITION
卷 151, 期 7, 页码 1894-1900

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jn/nxab053

关键词

selenium; age; type 2 diabetes; glucose intolerance; insulin resistance

资金

  1. NIH [DK117407]
  2. USDA, Agricultural Research Service, CRIS project [3062-51000-050-00D]
  3. National Institute of Food and Agriculture [1021193, MIS-384060, NE1939]

向作者/读者索取更多资源

The study found that mice fed diets containing <= 0.10 mg Se/kg displayed impaired glucose tolerance and insulin sensitivity, suggesting increased susceptibility to type 2 diabetes by suboptimal Se status at levels <= 23% of nutritional needs.
Background: Although dietary selenium (Se) deficiency or excess induces type 2 diabetes-like symptoms in mice, suboptimal body Se status usually causes no symptoms but may promote age-related decline in overall health. Objectives: We sought to determine the dietary Se requirement for protection against type 2 diabetes-like symptoms in mice. Methods: Thirty mature (aged 4 mo) male C57BU6J mice were fed a Se-deficient torula yeast AIN-93M diet supplemented with Na2SeO4 in graded concentrations totaling 0.01 (basal), 0.04, 0.07, 0.10, and 0.13 (control) mg Se/kg for 4 mo (n = 6) until they were middle-aged (8 mo). Droplets of whole blood were used to determine glucose tolerance and insulin sensitivity in the mice from ages 5 to 8 mo. Postmortem serum, liver, and skeletal muscle were collected to assay for selenoprotein expression and markers of glucose metabolism. Data were analyzed by 1-way ANCOVA with or without random effects for time-repeated measurements using live mice or postmortem samples, respectively. Results: Compared with control, the consumption of basal diet increased (P < 0.05) fasting serum insulin (95% CI: 52%, 182%) and leptin (95% CI: 103%, 118%) concentrations in middle-aged mice. Dietary Se insufficiency decreased (P < 0.05) 1) glucose tolerance (13-79%) and insulin sensitivity (15-65%) at <= 0.10 mg Se/kg; 2) baseline thymoma viral proto-oncogene phosphorylation on S473 (27-54%) and T308 (22-46%) at <= 0.10 and <= 0.07 mg Se/kg, respectively, in the muscle but not the liver; and 3) serum glutathione peroxidase 3 (51-83%), liver and muscle glutathione peroxidase 1 (32-84%), serum and liver selenoprotein P (28-42%), and liver and muscle selenoprotein H (39-48%) and selenoprotein W (16-73%) protein concentrations at <= 0.04, <= 0.10, <= 0.07, and <= 0.10 mg Se/kg, respectively. Conclusions: Mice fed diets containing <= 0.10 mg Se/kg display impaired glucose tolerance and insulin sensitivity, suggesting increased susceptibility to type 2 diabetes by suboptimal Se status at levels <= 23% of nutritional needs.

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