首页> 美国卫生研究院文献>NPJ Aging and Mechanisms of Disease >Both overlapping and independent mechanisms determine how diet and insulin-ligand knockouts extend lifespan of Drosophila melanogaster
【2h】

Both overlapping and independent mechanisms determine how diet and insulin-ligand knockouts extend lifespan of Drosophila melanogaster

机译:重叠和独立的机制决定了饮食和胰岛素-配体敲除如何延长果蝇的寿命

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Lifespan in many organisms, including Drosophila melanogaster, can be increased by reduced insulin-IGF-like signaling (IIS) or by changes in diet. Most studies testing whether IIS is involved in diet-mediated lifespan extension employ only a few diets, but recent data shows that a broad range of nutritional environments is required. Here, we present lifespan data of long-lived Drosophila, lacking three of the eight insulin-like peptides [Drosophila insulin-like peptides 2,3,5 (dilp2-3,5)] on nine different diets that surround the optimum for lifespan. Their nutritional content was varied by manipulating sugar and yeast concentrations independently, and thus incorporated changes in both diet restriction and nutrient balance. The mutants were substantially longer-lived than controls on every diet, but the effects on the lifespan response to sugar and yeast differed. Our data illustrates how a greater coverage of diet balance (DB) and restriction can unify differing interpretations of how IIS might be involved in the response of lifespan to diet.
机译:通过减少胰岛素-IGF样信号(IIS)或改变饮食,可以延长包括果蝇在内的许多生物的寿命。大多数测试IIS是否参与饮食介导的寿命延长的研究仅采用几种饮食,但最新数据表明需要广泛的营养环境。在这里,我们提供了长寿果蝇的寿命数据,它们缺乏围绕九种最佳饮食的八种胰岛素样肽[果蝇胰岛素样肽2,3,5(dilp2-3,5)]中的三种。它们的营养含量通过分别控制糖和酵母的浓度而变化,因此在饮食限制和营养平衡方面都进行了改变。在每种饮食中,突变体的寿命都比对照组长得多,但是对糖和酵母的寿命响应的影响却不同。我们的数据说明了如何更好地覆盖饮食平衡(DB)和限制饮食可以统一对IIS如何参与寿命对饮食的反应的不同解释。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号