Anderton B H
Department of Neuroscience, Institute of Psychiatry, De Crespigny Park, London.
Philos Trans R Soc Lond B Biol Sci. 1997 Dec 29;352(1363):1781-92. doi: 10.1098/rstb.1997.0162.
The brains of individuals, who are cognitively normal, show age-related changes that include an overall reduction in brain volume and weight, which are associated with gyral atrophy and widening of the sulci of the cerebral cortex, and enlargement of the brain ventricles. These changes are partly the result of nerve cell loss but accurate estimates of neuronal loss are notoriously difficult to make. Microscopically, there are increasing amounts of the age-related pigment, lipofuscin, granulovacuolar degeneration in neurones, Hirano bodies, variable amounts of diffuse deposits of beta-amyloid in the parenchyma, the presence of neurofibrillary tangles mainly confined to the hippocampus and amygdala, and sparse numbers of senile plaques in these brain regions and also in other cortical areas. Of these changes, neurofibrillary tangles and senile plaques are the neuropathological hallmark of Alzheimer's disease in which they are more abundant and widespread. Alzheimer's disease has therefore been regarded as accelerated brain ageing; however, the realization that there is a strong genetic contribution to developing the disease at least implies that it may not be the inevitable, even if frequent, consequence of old age. Understanding the molecular basis of plaque and tangle formation is advancing greatly and is the main focus of research into the cellular and molecular changes observed in the ageing brain.
认知正常的个体大脑会出现与年龄相关的变化,包括脑容量和重量总体减少,这与脑回萎缩、大脑皮质沟回增宽以及脑室扩大有关。这些变化部分是神经细胞丢失的结果,但神经元丢失的准确估计 notoriously 难以得出。在显微镜下,与年龄相关的色素脂褐素含量增加、神经元出现颗粒空泡变性、 Hirano 小体、实质内β淀粉样蛋白的弥漫性沉积量各不相同、神经原纤维缠结主要局限于海马体和杏仁核,以及这些脑区和其他皮质区域有少量老年斑。在这些变化中,神经原纤维缠结和老年斑是阿尔茨海默病的神经病理学标志,在该病中它们更为丰富和广泛。因此,阿尔茨海默病被视为加速的脑衰老;然而,认识到该病的发生有很强的遗传因素,至少意味着它可能不是衰老不可避免的后果,即使衰老时这种情况很常见。对斑块和缠结形成分子基础的理解正在取得很大进展,这是对衰老大脑中观察到的细胞和分子变化进行研究的主要焦点。