Department of Nutritional Sciences, Obesity and Metabolic Health Laboratory, Texas Tech University, Lubbock, TX, USA.
Internal Medicine, Cell Biology and Biochemistry, Neuroscience/Pharmacology and Neurology, Texas Tech University Health Sciences Center, Lubbock, TX, USA.
Exp Clin Endocrinol Diabetes. 2021 Jul;129(7):519-527. doi: 10.1055/a-0961-7804. Epub 2019 Jul 24.
The declining ability to control blood glucose with advancement of age is an important health risk factor and may lead to insulin resistance, type-2-diabetes and Alzheimer's disease. Adenovirus 36(Ad36) improves glycemic control independent of insulin signaling(insulin sparing effect) as evidenced by cell, animal and observational human studies. This property of Ad36 may be useful in correcting aging-related glucose intolerance and related health conditions. Therefore, we determined the effect of Ad36 on glycemic control in older mice, to identify the age group that best responds to Ad36. Six, 12 or 20-month old C57Bl/6 mice on chow diet were each divided into weight-matched groups(mock-infected or Ad36-infected). Body weight was recorded weekly post infection (p.i.) and fasting glucose measured(week 0, 4, 8 and 20 p.i.). Blood glucose and serum insulin were measured during glucose tolerance test(week 0 and 16 p.i.). At week 20 p.i., animals were sacrificed, blood and tissues collected.
Mice from all age groups showed improvement in glucose clearance post Ad36 infection, but a more profound effect was observed in 6-month old mice compared with mock-infected mice. Under fed conditions though there was no difference in blood glucose at 20 wk p.i., interestingly, Ad36 reduced serum insulin in age groups old mice, compared with control mice.
These findings suggest Ad36 infected animals improve glycemic control and clear post-prandial gluco00000se increase without increasing insulin secretion in an insulin sparing manner. These beneficial effects provide strong evidence for developing Ad36-based approaches as a novel tool to attenuate age associated glucose intolerance.
随着年龄的增长,控制血糖的能力下降是一个重要的健康风险因素,可能导致胰岛素抵抗、2 型糖尿病和阿尔茨海默病。腺病毒 36(Ad36)通过细胞、动物和观察性人体研究证明,可改善血糖控制而不依赖胰岛素信号(胰岛素节约效应)。Ad36 的这种特性可能有助于纠正与年龄相关的葡萄糖耐量不良和相关健康状况。因此,我们确定了 Ad36 对老年小鼠血糖控制的影响,以确定对 Ad36 反应最佳的年龄组。6、12 或 20 月龄的 C57Bl/6 小鼠在普通饮食上分为体重匹配的组(mock 感染或 Ad36 感染)。感染后每周记录体重,在第 0、4、8 和 20 周测量空腹血糖。在第 0 和 16 周进行葡萄糖耐量试验时测量血糖和血清胰岛素。在第 20 周感染后,动物被处死,采集血液和组织。
所有年龄组的小鼠在 Ad36 感染后葡萄糖清除率均有所改善,但 6 月龄小鼠的效果比 mock 感染组更为显著。在进食状态下,尽管 20 周感染后血糖没有差异,但有趣的是,与对照小鼠相比,Ad36 降低了老年小鼠的血清胰岛素。
这些发现表明,Ad36 感染动物以胰岛素节约的方式改善血糖控制并清除餐后葡萄糖增加,而不增加胰岛素分泌。这些有益的效果为开发基于 Ad36 的方法提供了强有力的证据,可作为一种新的工具来减轻与年龄相关的葡萄糖耐量不良。