The effects of normal aging on myelin and nerve fibers: A review

被引:421
作者
Peters, A [1 ]
机构
[1] Boston Univ, Sch Med, Dept Anat & Neurobiol, Boston, MA 02118 USA
来源
JOURNAL OF NEUROCYTOLOGY | 2002年 / 31卷 / 8-9期
关键词
D O I
10.1023/A:1025731309829
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页码:581 / 593
页数:13
相关论文
共 82 条
[41]  
2-C
[42]   LOSS OF INTRACORTICAL MYELINATED FIBERS - A DISTINCTIVE AGE-RELATED ALTERATION IN THE HUMAN STRIATE AREA [J].
LINTL, P ;
BRAAK, H .
ACTA NEUROPATHOLOGICA, 1983, 61 (3-4) :178-182
[43]  
Ludwin Samuel K., 1995, P412
[44]  
LUDWIN SK, 1978, LAB INVEST, V39, P597
[45]   The pathobiology of the oligodendrocyte [J].
Ludwin, SK .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1997, 56 (02) :111-124
[46]  
LUDWIN SK, 1988, J NEUROSCI, V8, P1239
[47]  
Malamud N., 1973, ATLAS NEUROPATHOLOGY
[48]  
MONIKI ES, 1995, AXON STRUCTURE FUNCT, P144
[49]   BASIC ELECTROPHYSIOLOGICAL PROPERTIES OF SPINAL-CORD MOTONEURONS DURING OLD-AGE IN THE CAT [J].
MORALES, FR ;
BOXER, PA ;
FUNG, SJ ;
CHASE, MH .
JOURNAL OF NEUROPHYSIOLOGY, 1987, 58 (01) :180-194
[50]   Life and death of neurons in the aging brain [J].
Morrison, JH ;
Hof, PR .
SCIENCE, 1997, 278 (5337) :412-419