Affiliation:
1. School of Medicine, Chiba University , Chiba , Japan
2. Department of Endocrinology, Hematology, and Gerontology, Chiba University Graduate School of Medicine , Chiba , Japan
Abstract
Abstract
Aging is believed to induce insulin resistance in humans. However, when and how insulin sensitivity changes with aging remains unclear in both humans and mice. In this study, groups of male C57BL/6N mice at 9–19 weeks (young), 34–67 weeks (mature adult), 84–85 weeks (presenile), and 107–121 weeks of age underwent hyperinsulinemic–euglycemic clamp studies with somatostatin infusion under awake and nonrestrained conditions. The glucose infusion rates for maintaining euglycemia were 18.4 ± 2.9, 5.9 ± 1.3, 20.3 ± 7.2, and 25.3 ± 4.4 mg/kg/min in young, mature adult, presenile, and aged mice, respectively. Thus, compared with young mice, mature adult mice exhibited the expected insulin resistance. In contrast, presenile and aged mice showed significantly higher insulin sensitivity than mature adult mice. These age-related changes were mainly observed in glucose uptake into adipose tissue and skeletal muscle (rates of glucose disappearance were 24.3 ± 2.0, 17.1 ± 1.0, 25.5 ± 5.2, and 31.8 ± 2.9 mg/kg/min in young, mature adult, presenile, and aged mice, respectively). Epididymal fat weight and hepatic triglyceride levels were higher in mature adult mice than those in young and aged mice. Our observations indicate that, in male C57BL/6N mice, insulin resistance appears at the mature adult stage of life but subsequently improves markedly. These alterations in insulin sensitivity are attributable to changes in visceral fat accumulations and age-related factors.
Funder
JSPS KAKENHI
Project for Elucidating and Controlling Mechanisms of Aging and Longevity of AMED
Institute of Medical Science, Asahi Life Foundation
Kashiwado Memorial Foundation for Medical Research
Publisher
Oxford University Press (OUP)
Subject
Geriatrics and Gerontology,Aging