Wu Pu, Shen Qian, Dong Suzhen, Xu Zhiliang, Tsien Joe Z, Hu Yinghe
Shanghai Institute of Brain Functional Genomics, MOE & STCSM Key Lab of Brain Functional Genomics, East China Normal University, Shanghai 200062, China.
Neurobiol Aging. 2008 Oct;29(10):1502-11. doi: 10.1016/j.neurobiolaging.2007.03.028. Epub 2007 May 17.
Conditional double knockout of presenilin-1 and presenilin-2 (cDKO) in forebrain of mice led to brain atrophy, tau hyperphosphorylation, synaptic dysfunction and cognitive deficit. These brain changes recapitulated most of the neurodegenerative phenotypes of Alzheimer's disease (AD). In this report, we have investigated the effects of 4-month calorie restriction (CR) regimen on different phenotypes in cDKO mice. We found that CR improved novel object recognition and contextual fear conditioning memory in the cDKO mice. Histological and biochemical analysis showed that CR attenuated ventricle enlargement, caspase-3 activation and astrogliosis. In addition, the induction of tau hyperphosphorylation in the cDKO mice was reduced by CR, possibly through reduction of p25 accumulation and aberrant CDK5 activation. Finally, DNA microarray analysis demonstrated that CR could increase the expression of neurogenesis related genes and decrease the expression of inflammation related genes in the hippocampus of cDKO mice. The possible molecular mechanisms of the CR effects on alleviating AD pathogenesis have been discussed.
小鼠前脑早老素-1和早老素-2条件性双敲除(cDKO)导致脑萎缩、tau蛋白过度磷酸化、突触功能障碍和认知缺陷。这些脑部变化重现了阿尔茨海默病(AD)的大多数神经退行性表型。在本报告中,我们研究了4个月热量限制(CR)方案对cDKO小鼠不同表型的影响。我们发现CR改善了cDKO小鼠的新物体识别和情境恐惧条件反射记忆。组织学和生化分析表明,CR减轻了脑室扩大、caspase-3激活和星形胶质细胞增生。此外,CR可能通过减少p25积累和异常的CDK5激活,降低了cDKO小鼠中tau蛋白过度磷酸化的诱导。最后,DNA微阵列分析表明,CR可增加cDKO小鼠海马体中神经发生相关基因的表达,并降低炎症相关基因的表达。本文还讨论了CR减轻AD发病机制的可能分子机制。