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正常衰老对恒河猴前额叶46区的影响。

Effects of normal aging on prefrontal area 46 in the rhesus monkey.

作者信息

Luebke Jennifer, Barbas Helen, Peters Alan

机构信息

Department of Anatomy & Neurobiology, Boston University School of Medicine, Boston, MA, USA.

出版信息

Brain Res Rev. 2010 Mar;62(2):212-32. doi: 10.1016/j.brainresrev.2009.12.002. Epub 2009 Dec 11.

Abstract

This review is concerned with the effects of normal aging on the structure and function of prefrontal area 46 in the rhesus monkey (Macaca mulatta). Area 46 has complex connections with somatosensory, visual, visuomotor, motor, and limbic systems and a key role in cognition, which frequently declines with age. An important question is what alterations might account for this decline. We are nowhere near having a complete answer, but as will be shown in this review, it is now evident that there is no single underlying cause. There is no significant loss of cortical neurons and although there are a few senile plaques in rhesus monkey cortex, their frequency does not correlate with cognitive decline. However, as discussed in this review, the following do correlate with cognitive decline. Loss of white matter has been proposed to result in some disconnections between parts of the central nervous system and changes in the structure of myelin sheaths reduce conduction velocity and the timing in neuronal circuits. In addition, there are reductions in the inputs to cortical neurons, as shown by regression of dendritic trees, loss of dendritic spines and synapses, and alterations in transmitters and receptors. These factors contribute to alterations in the intrinsic and network physiological properties of cortical neurons. As more details emerge, it is to be hoped that effective interventions to retard cognitive decline can be proposed.

摘要

本综述关注正常衰老对恒河猴(猕猴)前额叶46区结构和功能的影响。46区与体感、视觉、视运动、运动和边缘系统有着复杂的联系,并且在认知中起关键作用,而认知功能常常会随着年龄增长而衰退。一个重要的问题是,哪些改变可能导致了这种衰退。我们远未找到完整的答案,但正如本综述中将表明的,现在很明显不存在单一的潜在原因。皮质神经元没有显著损失,并且尽管在恒河猴皮质中有一些老年斑,但其出现频率与认知衰退并无关联。然而,正如本综述中所讨论的,以下因素确实与认知衰退相关。有人提出白质损失会导致中枢神经系统各部分之间的一些连接中断,并且髓鞘结构的变化会降低传导速度以及神经元回路中的时间同步性。此外,皮质神经元的输入减少,表现为树突树退化、树突棘和突触丢失以及递质和受体的改变。这些因素导致皮质神经元的内在和网络生理特性发生改变。随着更多细节的出现,希望能够提出有效的干预措施来延缓认知衰退。

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