雄性小鼠保留了在成年后短期饮食限制期间诱发的葡萄糖耐量改善的代谢记忆。

Longevity & healthspan Pub Date : 2012-09-03 eCollection Date: 2012-01-01 DOI:10.1186/2046-2395-1-3
Kerry M Cameron, Satomi Miwa, Cornelia Walker, Thomas von Zglinicki
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引用次数: 0

摘要

背景:慢性饮食限制(DR)已被证明对葡萄糖稳态和胰岛素敏感性有好处。当啮齿类动物在中年期从自由饮食(AL)过渡到 DR 时,这些因素会得到迅速而有力的改善。我们的目的是确定当恢复 AL 饲喂(AL-DR-AL)时,短期暴露于 DR 所诱导的有益影响是否能作为 "代谢记忆 "保留下来,反之亦然:长期 DR 的影响是否能通过一段时间的 AL 饲喂而逆转(DR-AL-DR)。使用 C57BL/6 雄性和雌性小鼠研究性别差异(N = 10/性别/组)。小鼠从 3 个月到 15 个月期间(基线)喂食 AL 或 DR,每次饮食交叉持续约 5 个月:结果:雌性小鼠的体重和脂肪量与喂养方式的变化成正比,血浆胰岛素和葡萄糖耐量不受交叉喂养的影响。然而,雄性小鼠的葡萄糖耐量和血浆胰岛素水平在 6 至 12 周内发生逆转。当雄性小鼠在5个月的DR(AL-DR-AL)后恢复AL摄入时,体重保持在基线以下,与脂肪量的变化成正比。葡萄糖耐量也明显优于基线:结论:雄性小鼠保留了饲喂 5 个月 DR 的代谢记忆,即体重减轻和葡萄糖耐量改善。这意味着,即使恢复自由摄食,至少对雄性小鼠来说,成年后一段时间的DR诱导的一些有益影响可能是有益的。然而,在持续摄入DR的情况下,雌性动物的寿命延长比雄性动物更明显。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction.

Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction.

Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction.

Male mice retain a metabolic memory of improved glucose tolerance induced during adult onset, short-term dietary restriction.

Background: Chronic dietary restriction (DR) has been shown to have beneficial effects on glucose homeostasis and insulin sensitivity. These factors show rapid and robust improvements when rodents were crossed over from an ad libitum (AL) diet to DR in mid life. We aimed to determine whether the beneficial effects induced by short-term exposure to DR can be retained as a 'metabolic memory' when AL feeding is resumed (AL-DR-AL) and vice versa: whether the effects of long-term DR can be reversed by a period of AL feeding (DR-AL-DR). C57BL/6 male and female mice were used to examine sex differences (N = 10/sex/group). Mice were fed AL or DR from 3 until 15 months (baseline) and each dietary crossover lasted approximately 5 months.

Results: In females, body and fat mass were proportional to the changes in feeding regime and plasma insulin and glucose tolerance were unaffected by the crossovers. However, in male mice, glucose tolerance and plasma insulin levels were reversed within 6 to 12 weeks. When males returned to AL intake following 5 months DR (AL-DR-AL), body mass was maintained below baseline, proportional to changes in fat mass. Glucose tolerance was also significantly better compared to baseline.

Conclusions: Male mice retained a metabolic memory of 5 months of DR feeding in terms of reduced body mass and improved glucose tolerance. This implies that some of the beneficial effects induced by a period of DR in adult life may be beneficial, even when free feeding is resumed at least in males. However, under continuous DR, lifespan extension was more prominent in females than in males.

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