首页> 外文期刊>Journal of Neurocytology: A Journal of Cellular Neurobiology >The effects of normal aging on myelin and nerve fibers: A review.
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The effects of normal aging on myelin and nerve fibers: A review.

机译:正常衰老对髓鞘和神经纤维的影响:综述。

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It was believed that the cause of the cognitive decline exhibited by human and non-human primates during normal aging was a loss of cortical neurons. It is now known that significant numbers of cortical neurons are not lost and other bases for the cognitive decline have been sought. One contributing factor may be changes in nerve fibers. With age some myelin sheaths exhibit degenerative changes, such as the formation of splits containing electron dense cytoplasm, and the formation on myelin balloons. It is suggested that such degenerative changes lead to cognitive decline because they cause changes in conduction velocity, resulting in a disruption of the normal timing in neuronal circuits. Yet as degeneration occurs, other changes, such as the formation of redundant myelin and increasing thickness suggest of sheaths, suggest some myelin formation is continuing during aging. Another indication of this is that oligodendrocytes increase in number with age.In addition to the myelin changes, stereological studies have shown a loss of nerve fibers from the white matter of the cerebral hemispheres of humans, while other studies have shown a loss of nerve fibers from the optic nerves and anterior commissure in monkeys. It is likely that such nerve fiber loss also contributes to cognitive decline, because of the consequent decrease in connections between neurons.Degeneration of myelin itself does not seem to result in microglial cells undertaking phagocytosis. These cells are probably only activated when large numbers of nerve fibers are lost, as can occur in the optic nerve.
机译:据信在正常衰老过程中人类和非人类灵长类动物所表现出的认知能力下降的原因是皮质神经元的丧失。现在已知,没有大量的皮质神经元丢失,并且已经寻求了其他认知下降的基础。一种促成因素可能是神经纤维的变化。随着年龄的增长,一些髓鞘鞘表现出退化性变化,例如含有电子致密细胞质的裂痕的形成以及在髓鞘球囊上的形成。提示这种退行性改变会导致认知能力下降,因为它们会引起传导速度的改变,从而导致神经元回路正常计时的中断。然而,随着变性的发生,其他变化,例如多余的髓磷脂的形成和增加的鞘厚度表明,在衰老过程中一些髓磷脂的形成仍在继续。另一个迹象表明少突胶质细胞的数量会随着年龄的增长而增加。除了髓磷脂的变化外,立体研究还显示出人脑半球白质中神经纤维的减少,而其他研究则表明神经纤维的减少。来自猴子的视神经和前连合。由于神经元之间的连接减少,这种神经纤维的损失也可能导致认知能力的下降。髓磷脂本身的变性似乎并不导致小胶质细胞发生吞噬作用。这些细胞可能仅在大量神经纤维丢失时才被激活,这可能发生在视神经中。

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