The role of neuronal growth factors in neurodegenerative disorders of the human brain

被引:492
作者
Connor, B
Dragunow, M
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Dept Pharmacol, Auckland 1, New Zealand
[2] Univ Auckland, Fac Med & Hlth Sci, Dept Mol Med, Auckland 1, New Zealand
关键词
NGF; BDNF; NT-3; GDNF; IGF-I; TGF-alpha; trk receptor; neurodegeneration; neurotrophin;
D O I
10.1016/S0165-0173(98)00004-6
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent evidence suggests that neurotrophic factors that promote the survival or differentiation of developing neurons may also protect mature neurons from neuronal atrophy in the degenerating human brain. Furthermore, it has been proposed that the pathogenesis of human neurodegenerative disorders may be due to an alteration in neurotrophic factor and/or trk receptor levels. The use of neurotrophic factors as therapeutic agents is a novel approach aimed at restoring and maintaining neuronal function in the central nervous system (CNS). Research is currently being undertaken to determine potential mechanisms to deliver neurotrophic factors to selectively vulnerable regions of the CNS. However, while there is widespread interest in the use of neurotrophic factors to prevent and/or reduce the neuronal cell loss and atrophy observed in neurodegenerative disorders, little research has been performed examining the expression and functional role of these factors in the normal and diseased human brain. This review will discuss recent studies and examine the role members of the nerve growth factor family (NGF, BDNF and NT-3) and trk receptors as well as additional growth factors (GDNF, TGF-alpha and IGF-I) may play in neurodegenerative disorders of the human brain. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
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页码:1 / 39
页数:39
相关论文
共 498 条
[11]  
ALEXIANU ME, 1994, J NEUROCHEM, V63, P2365
[12]   NORMAL BETA-NGF CONTENT IN ALZHEIMERS-DISEASE CEREBRAL-CORTEX AND HIPPOCAMPUS [J].
ALLEN, SJ ;
MACGOWAN, SH ;
TREANOR, JJS ;
FEENEY, R ;
WILCOCK, GK ;
DAWBARN, D .
NEUROSCIENCE LETTERS, 1991, 131 (01) :135-139
[13]   DISTRIBUTION OF BETA-NERVE GROWTH-FACTOR RECEPTORS IN THE HUMAN BASAL FOREBRAIN [J].
ALLEN, SJ ;
DAWBARN, D ;
SPILLANTINI, MG ;
GOEDERT, M ;
WILCOCK, GK ;
MOSS, TH ;
SEMENENKO, FM .
JOURNAL OF COMPARATIVE NEUROLOGY, 1989, 289 (04) :626-640
[14]   PROGRAMMED CELL-DEATH - THE PATHS TO SUICIDE [J].
ALTMAN, J .
TRENDS IN NEUROSCIENCES, 1992, 15 (08) :278-280
[15]   DNA damage and apoptosis in Alzheimer's disease: Colocalization with c-Jun immunoreactivity, relationship to brain area, and effect of postmortem delay [J].
Anderson, AJ ;
Su, JH ;
Cotman, CW .
JOURNAL OF NEUROSCIENCE, 1996, 16 (05) :1710-1719
[16]  
ANDERSON AJ, 1995, J NEUROCHEM, V65, P1487
[17]   INCREASED IMMUNOREACTIVITY FOR JUN-RELATED AND FOS-RELATED PROTEINS IN ALZHEIMERS-DISEASE - ASSOCIATION WITH PATHOLOGY [J].
ANDERSON, AJ ;
CUMMINGS, BJ ;
COTMAN, CW .
EXPERIMENTAL NEUROLOGY, 1994, 125 (02) :286-295
[18]   Ciliary neurotrophic factor protects striatal output neurons in an animal model of Huntington disease [J].
Anderson, KD ;
Panayotatos, N ;
Corcoran, TL ;
Lindsay, RM ;
Wiegand, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (14) :7346-7351
[19]  
Anglade P, 1997, HISTOL HISTOPATHOL, V12, P25
[20]  
[Anonymous], HUMAN HIPPOCAMPUS