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正常衰老对猴中枢神经系统有髓神经纤维的影响。

The effects of normal aging on myelinated nerve fibers in monkey central nervous system.

机构信息

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

出版信息

Front Neuroanat. 2009 Jul 6;3:11. doi: 10.3389/neuro.05.011.2009. eCollection 2009.

Abstract

The effects of aging on myelinated nerve fibers of the central nervous system are complex. Many myelinated nerve fibers in white matter degenerate and are lost, leading to some disconnections between various parts of the central nervous system. Other myelinated nerve fibers are affected differently, because only their sheaths degenerate, leaving the axons intact. Such axons are remyelinated by a series of internodes that are much shorter than the original ones and are composed of thinner sheaths. Thus the myelin-forming cells of the central nervous system, the oligodendrocytes, remain active during aging. Indeed, not only do these neuroglial cell remyelinate axons, with age they also continue to add lamellae to the myelin sheaths of intact nerve fibers, so that sheaths become thicker. It is presumed that the degeneration of myelin sheaths is due to the degeneration of the parent oligodendrocyte, and that the production of increased numbers of internodes as a consequence of remyelination requires additional oligodendrocytes. Whether there is a turnover of oligodendrocytes during life has not been studied in primates, but it has been established that over the life span of the monkey, there is a substantial increase in the numbers of oligodendrocytes. While the loss of some myelinated nerve fibers leads to some disconnections, the degeneration of other myelin sheaths and the subsequent remyelination of axons by shorter internodes slow down the rate conduction along nerve fibers. These changes affect the integrity and timing in neuronal circuits, and there is evidence that they contribute to cognitive decline.

摘要

衰老对中枢神经系统有髓神经纤维的影响很复杂。许多白质中的有髓神经纤维退化并丢失,导致中枢神经系统的各个部分之间出现一些连接中断。其他有髓神经纤维受到不同的影响,因为只有它们的髓鞘退化,而轴突保持完整。这些轴突被一系列比原来短得多的节段重新髓鞘化,其髓鞘较薄。因此,中枢神经系统的髓鞘形成细胞,即少突胶质细胞,在衰老过程中仍然保持活跃。事实上,这些神经胶质细胞不仅对轴突进行再髓鞘化,而且随着年龄的增长,它们还继续在完整神经纤维的髓鞘上添加板层,使髓鞘变厚。髓鞘退化被认为是由于亲代少突胶质细胞的退化,而由于再髓鞘化而产生更多的节段需要额外的少突胶质细胞。在灵长类动物中,是否有少突胶质细胞的更替尚不清楚,但已经确定,在猴子的一生中,少突胶质细胞的数量会大量增加。虽然一些有髓神经纤维的丢失会导致一些连接中断,但其他髓鞘的退化和随后轴突通过更短的节段的重新髓鞘化会减缓神经纤维的传导速度。这些变化会影响神经元回路的完整性和时间安排,有证据表明它们会导致认知能力下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb8f/2713738/b1675b9d8eb8/fnana-03-011-g001.jpg

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