Terzibasi Eva, Lefrançois Christel, Domenici Paolo, Hartmann Nils, Graf Michael, Cellerino Alessandro
Biology of Aging, Fritz Lipmann Institute for Age Research, Leibniz Institute, Jena 07745 Germany.
Aging Cell. 2009 Apr;8(2):88-99. doi: 10.1111/j.1474-9726.2009.00455.x.
The short-lived annual fish Nothobranchius furzeri shows extremely short captive life span and accelerated expression of age markers, making it an interesting model system to investigate the effects of experimental manipulations on longevity and age-related pathologies. Here, we tested the effects of dietary restriction (DR) on mortality and age-related markers in N. furzeri. DR was induced by every other day feeding and the treatment was performed both in an inbred laboratory line and a longer-lived wild-derived line. In the inbred laboratory line, DR reduced age-related risk and prolonged maximum life span. In the wild-derived line, DR induced early mortality, did not reduce general age-related risk and caused a small but significant extension of maximum life span. Analysis of age-dependent mortality revealed that DR reduced demographic rate of aging, but increased baseline mortality in the wild-derived strain. In both inbred- and wild-derived lines, DR prevented the expression of the age markers lipofuscin in the liver and Fluoro-Jade B (neurodegeneration) in the brain. DR also improved performance in a learning test based on conditioning (active avoidance in a shuttle box). Finally, DR induced a paradoxical up-regulation of glial fibrillary acidic protein in the brain.
短命的一年生鱼类费氏假鳃鳉表现出极短的圈养寿命和加速的衰老标志物表达,使其成为研究实验操作对寿命和年龄相关病理影响的有趣模型系统。在此,我们测试了饮食限制(DR)对费氏假鳃鳉死亡率和年龄相关标志物的影响。通过隔天喂食诱导饮食限制,该处理在一个近交实验室品系和一个寿命更长的野生衍生品系中均进行。在近交实验室品系中,饮食限制降低了与年龄相关的风险并延长了最大寿命。在野生衍生品系中,饮食限制导致早期死亡,未降低一般与年龄相关的风险,但使最大寿命有小幅但显著的延长。对年龄依赖性死亡率的分析表明,饮食限制降低了衰老的人口统计学速率,但增加了野生衍生品系的基线死亡率。在近交和野生衍生品系中,饮食限制均阻止了肝脏中脂褐素和大脑中氟玉红B(神经退行性变)等衰老标志物的表达。饮食限制还改善了基于条件反射(穿梭箱中的主动回避)的学习测试中的表现。最后,饮食限制诱导了大脑中胶质纤维酸性蛋白的矛盾性上调。