Insulin-like growth factors in the treatment of neurological disease

被引:34
作者
Leinninger, GM
Feldman, EL
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Program Neurosci, Ann Arbor, MI 48109 USA
来源
IGF-I AND IGF BINDING PROTEINS: BASIC RESEARCH AND CLINICAL MANAGEMENT | 2005年 / 9卷
关键词
D O I
10.1159/000085763
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although the functional deficits of neurological diseases vary, they are all pathologically marked by neuronal degeneration. The ability of insulin-like growth factor-1 (IGF-I) to support both sensory and motor neuron regeneration has suggested its potential in treatment of neurological diseases. IGF-I is pleiotrophic, stimulating survival, neurite outgrowth and motility in neurons, as well as myelination of neurons by glia. Understanding the intracellular signaling pathways that mediate these pleiotrophic responses to IGF-1 is important for tailoring IGF-I treatment to the appropriate neurological deficit. This review surveys the current understanding of IGF-I pleiotrophism, the underlying signaling conferring these effects, and the status of IGF-I in treatment of human neurological disorders. Copyright (c) 2005 S. Karger AG, Basel.
引用
收藏
页码:135 / 159
页数:25
相关论文
共 128 条
[1]   LOCOMOTION OF FIBROBLASTS IN CULTURE .4. ELECTRON MICROSCOPY OF LEADING LAMELLA [J].
ABERCROM.M ;
HEAYSMAN, JE ;
PEGRUM, SM .
EXPERIMENTAL CELL RESEARCH, 1971, 67 (02) :359-&
[2]   BRAIN NEURONS DEVELOP IN A SERUM AND GLIAL FREE ENVIRONMENT - EFFECTS OF TRANSFERRIN, INSULIN, INSULIN-LIKE GROWTH FACTOR-I AND THYROID-HORMONE ON NEURONAL SURVIVAL, GROWTH AND DIFFERENTIATION [J].
AIZENMAN, Y ;
DEVELLIS, J .
BRAIN RESEARCH, 1987, 406 (1-2) :32-42
[3]   Recombinant human nerve growth factor in the treatment of diabetic polyneuropathy [J].
Apfel, SC ;
Kessler, JA ;
Adornato, BT ;
Litchy, WJ ;
Sanders, C ;
Rask, CA .
NEUROLOGY, 1998, 51 (03) :695-702
[4]  
AYERLELIEVRE C, 1991, DEVELOPMENT, V111, P105
[5]   EXPRESSION OF PO PROTEIN MESSENGER-RNA ALONG RAT SCIATIC-NERVE DURING DEVELOPMENT [J].
BARON, P ;
SHY, M ;
KAMHOLZ, J ;
SCARLATO, G ;
PLEASURE, D .
DEVELOPMENTAL BRAIN RESEARCH, 1994, 83 (02) :285-288
[6]   IGF1 GENE DISRUPTION RESULTS IN REDUCED BRAIN SIZE, CNS HYPOMYELINATION, AND LOSS OF HIPPOCAMPAL GRANULE AND STRIATAL PARVALBUMIN-CONTAINING NEURONS [J].
BECK, KD ;
POWELLBRAXTON, L ;
WIDMER, HR ;
VALVERDE, J ;
HEFTI, F .
NEURON, 1995, 14 (04) :717-730
[7]   Delayed application of IGF-1 and GDNF can rescue already injured postnatal motor neurons [J].
Bilak, MM ;
Kuncl, RW .
NEUROREPORT, 2001, 12 (11) :2531-2535
[8]   CELLULAR-PATTERN OF INSULIN-LIKE GROWTH FACTOR-I (IGF-I) AND TYPE-I IGF RECEPTOR GENE-EXPRESSION IN EARLY ORGANOGENESIS - COMPARISON WITH IGF-II GENE-EXPRESSION [J].
BONDY, CA ;
WERNER, H ;
ROBERTS, CT ;
LEROITH, D .
MOLECULAR ENDOCRINOLOGY, 1990, 4 (09) :1386-1398
[9]   A placebo-controlled trial of insulin-like growth factor-I in amyotrophic lateral sclerosis [J].
Borasio, GD ;
Robberecht, W ;
Leigh, PN ;
Emile, J ;
Guiloff, RJ ;
Jerusalem, F ;
Silani, V ;
Vos, PE ;
Wokke, JHJ ;
Dobbins, T .
NEUROLOGY, 1998, 51 (02) :583-586
[10]   STUDIES ON CULTURED RAT SCHWANN-CELLS .3. ASSAYS FOR PERIPHERAL MYELIN PROTEINS [J].
BROCKES, JP ;
RAFF, MC ;
NISHIGUCHI, DJ ;
WINTER, J .
JOURNAL OF NEUROCYTOLOGY, 1980, 9 (01) :67-77