Axonal degeneration in the pathogenesis of multiple sclerosis

被引:81
作者
Silber, E [1 ]
Sharief, MK [1 ]
机构
[1] Kings Coll London, Guys Kings & St Thomas Sch Med, Dept Clin Neurosci, London WC2R 2LS, England
关键词
multiple sclerosis; axon;
D O I
10.1016/S0022-510X(99)00178-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Axonal degeneration plays an important role in the accumulation of disability in patients with multiple sclerosis (MS). Pathological studies have demonstrated axonal damage, particularly in areas of acute inflammation and demyelination, and in chronic lesions. Axonal loss and its progression, which is associated with neurological disability, has also been demonstrated by magnetic resonance imaging (MRI) studies. The mechanisms of axonal loss are uncertain, but may involve axonal degeneration secondary to demyelination, or damage to the axonal cytoskeleton. Inflammatory mediators, including cytokines and proteolytic enzymes may contribute to axonal damage, as may nitric oxide. Axonal destruction may also be due to immune attack directed at axonal components. The realisation that axonal degeneration is a fundamental component of MS that may occur early in the disease course should alter the approach to management and open avenues to a more targeted immunotherapy aimed at reducing the progression of disability. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:11 / 18
页数:8
相关论文
共 97 条
[71]   An enzyme immunoassay for neuron-specific enolase in cerebrospinal fluid [J].
Orlino, EN ;
Olmstead, CE ;
Lazareff, JA ;
Peacock, WJ ;
Fisher, RS ;
Fluharty, AL .
BIOCHEMICAL AND MOLECULAR MEDICINE, 1997, 61 (01) :41-46
[72]   PATTERNS OF OLIGODENDROGLIA PATHOLOGY IN MULTIPLE-SCLEROSIS [J].
OZAWA, K ;
SUCHANEK, G ;
BREITSCHOPF, H ;
BRUCK, W ;
BUDKA, H ;
JELLINGER, K ;
LASSMANN, H .
BRAIN, 1994, 117 :1311-1322
[73]   HEAT-SHOCK PROTEIN IMMUNOREACTIVITY IN CSF - CORRELATION WITH OLIGOCLONAL BANDING AND DEMYELINATING DISEASE [J].
PRABHAKAR, S ;
KURIEN, E ;
GUPTA, RS ;
ZIELINSKI, S ;
FREEDMAN, MS .
NEUROLOGY, 1994, 44 (09) :1644-1648
[74]   FINE-STRUCTURE OF CHRONICALLY ACTIVE MULTIPLE-SCLEROSIS PLAQUES [J].
PRINEAS, JW ;
CONNELL, F .
NEUROLOGY, 1978, 28 (09) :68-75
[75]  
RAINE CS, 1989, LAB INVEST, V60, P714
[76]   Nitric oxide donors reversibly block axonal conduction: demyelinated axons are especially susceptible [J].
Redford, EJ ;
Kapoor, R ;
Smith, KJ .
BRAIN, 1997, 120 :2149-2157
[77]   ULTRASTRUCTURE OF MULTIPLE-SCLEROSIS [J].
RODRIGUEZ, M ;
SCHEITHAUER, B .
ULTRASTRUCTURAL PATHOLOGY, 1994, 18 (1-2) :3-13
[78]   Patients with amyotrophic lateral sclerosis and other neurodegenerative diseases have increased levels of neurofilament protein in CSF [J].
Rosengren, LE ;
Karlsson, JE ;
Karlsson, JO ;
Persson, LI ;
Wikkelso, C .
JOURNAL OF NEUROCHEMISTRY, 1996, 67 (05) :2013-2018
[79]   REDUCED DIAMETER AND CONDUCTION-VELOCITY OF MYELINATED FIBERS IN THE SCIATIC-NERVE OF A NEUROFILAMENT-DEFICIENT MUTANT QUAIL [J].
SAKAGUCHI, T ;
OKADA, M ;
KITAMURA, T ;
KAWASAKI, K .
NEUROSCIENCE LETTERS, 1993, 153 (01) :65-68
[80]   AXONAL REGENERATION IN THE RAT SPINAL-CORD PRODUCED BY AN ANTIBODY AGAINST MYELIN-ASSOCIATED NEURITE GROWTH-INHIBITORS [J].
SCHNELL, L ;
SCHWAB, ME .
NATURE, 1990, 343 (6255) :269-272