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Late-onset intermittent fasting dietary restriction as a potential intervention to retard age-associated brain function impairments in male rats

机译:迟发性间歇性禁食饮食限制可作为延缓雄性大鼠年龄相关性脑功能障碍的潜在干预措施

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摘要

Lifelong dietary restriction (DR) is known to have many potential beneficial effects on brain function as well as delaying the onset of neurological diseases. In the present investigation, the effect of late-onset short-term intermittent fasting dietary restriction (IF-DR) regimen was studied on motor coordination and cognitive ability of ageing male rats. These animals were further used to estimate protein carbonyl content and mitochondrial complex I–IV activity in different regions of brain and peripheral organs, and the degree of age-related impairment and reversion by late-onset short-term IF-DR was compared with their levels in 3-month-old young rats. The results of improvement in motor coordination by rotarod test and cognitive skills by Morris water maze in IF-DR rats were found to be positively correlated with the decline in the oxidative molecular damage to proteins and enhanced mitochondrial complex IV activity in different regions of ageing brain as well as peripheral organs. The work was further extended to study the expression of synaptic plasticity-related proteins, such as synaptophysin, calcineurin and CaM kinase II to explore the molecular basis of IF-DR regimen to improve cognitive function. These results suggest that even late-onset short-term IF-DR regimen have the potential to retard age-associated detrimental effects, such as cognitive and motor performance as well as oxidative molecular damage to proteins.
机译:终身饮食限制(DR)已知对脑功能具有许多潜在的有益作用,并延缓了神经系统疾病的发作。在本研究中,研究了迟发短期间歇性空腹饮食限制(IF-DR)方案对衰老雄性大鼠运动协调和认知能力的影响。这些动物被进一步用于估计大脑和周围器官不同区域的蛋白质羰基含量和线粒体复合物I–IV活性,并将与晚期发作的短期IF-DR引起的年龄相关损伤和逆转程度进行比较。在3个月大的幼鼠中的水平。通过旋转脚架测试改善运动协调性并通过Morris水迷宫改善IF-DR大鼠的认知能力的结果与衰老的大脑不同区域中蛋白质的氧化分子损伤的减少和线粒体复合物IV活性的增强呈正相关。以及周围器官。这项工作进一步扩展到研究突触可塑性相关蛋白(如突触素,钙调神经磷酸酶和CaM激酶II)的表达,以探索IF-DR方案改善认知功能的分子基础。这些结果表明,即使是迟发的短期IF-DR疗法,也有可能延缓与年龄相关的有害影响,例如认知和运动表现以及蛋白质的氧化性分子损伤。

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