Ageing, Neuronal Connectivity and Brain Disorders: An Unsolved Ripple Effect

被引:28
作者
Bano, Daniele [1 ]
Agostini, Massimiliano [2 ]
Melino, Gerry [2 ,3 ,4 ]
Nicotera, Pierluigi [1 ]
机构
[1] DZNE, D-53175 Bonn, Germany
[2] Univ Leicester, MRC, Toxicol Unit, Leicester, Leics, England
[3] Univ Roma Tor Vergata, IDI IRCCS, Biochem Lab, Rome, Italy
[4] European Brain Res Inst, Rome, Italy
基金
英国医学研究理事会;
关键词
Ageing; Cognitive decline; MicroRNA; Mitochondria; Neurodegenerative disorders; Dendritic spine; PURKINJE-CELL-DEGENERATION; LIFE-SPAN EXTENSION; C-ELEGANS; MITOCHONDRIAL-FUNCTION; CALORIC RESTRICTION; SPINE CHANGES; MICE; AUTOPHAGY; LONGEVITY; DISEASE;
D O I
10.1007/s12035-011-8164-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cognitive decline associated with ageing and age-related disorders emerges as one of the greatest health challenges in the next decades. To date, the molecular mechanisms underlying the onset of neuronal physiological changes in the central nervous system remain unclear. Functional MRI and PET studies have indicated the decline in working memory performance in older adults. Similarly, age-related disorders, such as Alzheimer's disease, are associated with changes in the prefontral cortex and related neural circuitry, which underlines the decline of integrative function between different brain regions. This is mainly attributed to the loss of synaptic connectivity, which is a feature commonly observed in neurodegenerative disorders. In humans, the morphological and functional changes in neurons, such as reduction of spine numbers and synaptic dysfunction, precede the first signs of cognitive decline and likely contribute to pathology progression. Thus, a new scenario emerges in which apparently unrelated diseases present common features, such as the remodelling of neuronal circuitries promoted by ageing. For many years, ageing was considered a process of slow deterioration triggered by accidental environmental factors. Conversely, it is now evident that ageing is a biological process tightly controlled by evolutionary highly conserved signalling pathways. Importantly, genetic mutations that enhance longevity significantly delay the loss of synaptic connectivity and, therefore, the onset of age-related brain disorders. Accordingly, tweaking ageing might be an attractive approach to prevent cognitive decline caused by age-related synaptic dysfunction.
引用
收藏
页码:124 / 130
页数:7
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