White matter damage and degeneration in traumatic brain injury

被引:0
|
作者
Armstrong, Regina C. [1 ,2 ]
Sullivan, Genevieve M. [1 ,2 ,3 ]
Perl, Daniel P. [4 ,5 ]
Rosarda, Jessica D. [1 ]
Radomski, Kryslaine L. [1 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Anat Physiol & Genet, Bethesda, MD 20814 USA
[2] Mil Traumat Brain Injury Initiat, Bethesda, MD 20814 USA
[3] Henry M Jackson Fdn Adv Mil Med, Bethesda, MD USA
[4] Uniformed Serv Univ Hlth Sci, Sch Med, Pathol, Bethesda, MD USA
[5] Uniformed Serv Univ Brain Tissue Repository, Dept Def, Bethesda, MD USA
关键词
UNFOLDED PROTEIN RESPONSE; DIFFUSE AXONAL INJURY; MYELIN; MECHANISMS; OLIGODENDROCYTES; TENSOR; DYSFUNCTION; PATHOLOGY; ATROPHY; SINGLE;
D O I
10.1016/j.tins.2024.07.003
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Traumatic brain injury (TBI) is a complex condition that can resolve over time but all too often leads to persistent symptoms, and the risk of poor patient outcomes increases with aging. TBI damages neurons and long axons within white matter tracts that are critical for communication between brain regions; this causes slowed information processing and neuronal circuit dysfunction. This review focuses on white matter injury after TBI and the multifactorial processes that underlie white matter damage, potential for recovery, and progression of degeneration. A multiscale perspective across clinical and preclinical advances is presented to encourage interdisciplinary insights from whole-brain neuroimaging of white matter tracts down to cellular and molecular responses of axons, myelin, and glial cells within white matter tissue.
引用
收藏
页码:677 / 692
页数:16
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