The insulin-like growth factor I system in cerebellar degeneration

被引:47
作者
TorresAleman, I
Barrios, V
Lledo, A
Berciano, J
机构
[1] INST CAJAL,PSYCHOBIOL LAB,E-28002 MADRID,SPAIN
[2] HOSP NINO JESUS,DIV PEDIAT ENDOCRINOL,MADRID,SPAIN
[3] HOSP UNIV MARQUES VALDECILLA,DEPT NEUROL,SANTANDER,SPAIN
关键词
D O I
10.1002/ana.410390310
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Brain insulin-like growth factor I (IGF-I) and its related molecules may be involved in neurodegenerative processes in which IGF-I-containing pathways are compromised. Since IGF-I is present in the olivocerebellar circuitry, two types of late-onset cerebellar ataxias (olivopontocerebellar and idiopathic cerebellar cortical atrophy) were chosen to test this hypothesis. The following significant changes in the peripheral IGF-I system of these patients were found: low IGF-I levels, and high IGF-binding protein 1 (BP-1), and BP-3 affinity for IGF-1. Sixty percent of the patients also had significantly low insulin levels. Patients suffering from other neurological diseases with cerebellar dysfunction and ataxia not involving the olivocerebellar pathway also had low IGF-I levels, while IGFBPs and insulin levels were normal. Our data indicate that degeneration of an IGF-I-containing neuronal pathway produces significant changes in the peripheral IGF system. This suggests strongly that the endocrine (bloodborne) and the paracrine/autocrine (brain) IGF systems are linked functionally. We propose that alterations in the blood IGF-I system may constitute a marker of some cerebellar diseases.
引用
收藏
页码:335 / 342
页数:8
相关论文
共 51 条
[31]  
MARTY S, 1994, J NEUROSCI, V14, P5257
[32]   ORTHOGRADE TRANSPORT AND RELEASE OF INSULIN-LIKE GROWTH FACTOR-I FROM THE INFERIOR OLIVE TO THE CEREBELLUM [J].
NIETOBONA, MP ;
GARCIASEGURA, LM ;
TORRESALEMAN, I .
JOURNAL OF NEUROSCIENCE RESEARCH, 1993, 36 (05) :520-527
[33]   INSULIN-LIKE GROWTH-FACTOR-I IS AN AFFERENT TROPHIC SIGNAL THAT MODULATES CALBINDIN-28KD IN ADULT PURKINJE-CELLS [J].
NIETOBONA, MP ;
BUSIGUINA, S ;
TORRESALEMAN, I .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 42 (03) :371-376
[34]  
OPPENHEIMER DR, 1992, GREENFIELDS NEUROPAT
[35]   INSULIN-LIKE GROWTH FACTOR-I SHIFTS FROM PROMOTING CELL-DIVISION TO POTENTIATING MATURATION DURING NEURONAL DIFFERENTIATION [J].
PAHLMAN, S ;
MEYERSON, G ;
LINDGREN, E ;
SCHALLING, M ;
JOHANSSON, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (22) :9994-9998
[36]   HEREDITARY ATAXIAS AND PARAPLEGIAS IN CANTABRIA, SPAIN - AN EPIDEMIOLOGIC AND CLINICAL-STUDY [J].
POLO, JM ;
CALLEJA, J ;
COMBARROS, O ;
BERCIANO, J .
BRAIN, 1991, 114 :855-866
[37]   BASIC FIBROBLAST GROWTH-FACTOR MODULATES INSULIN-LIKE GROWTH FACTOR-I, ITS RECEPTOR, AND ITS BINDING-PROTEINS IN HYPOTHALAMIC CELL-CULTURES [J].
PONS, S ;
TORRESALEMAN, I .
ENDOCRINOLOGY, 1992, 131 (05) :2271-2278
[38]   ONTOGENY OF INSULIN-LIKE GROWTH FACTOR-I, ITS RECEPTOR, AND ITS BINDING-PROTEINS IN THE RAT HYPOTHALAMUS [J].
PONS, S ;
REJAS, MT ;
TORRESALEMAN, I .
DEVELOPMENTAL BRAIN RESEARCH, 1991, 62 (02) :169-175
[39]   INSULIN-LIKE GROWTH-FACTORS CROSS THE BLOOD-BRAIN-BARRIER [J].
REINHARDT, RR ;
BONDY, CA .
ENDOCRINOLOGY, 1994, 135 (05) :1753-1761
[40]  
REWCASTLE NB, 1991, TXB NEUROPATHOLOGY