Therapeutic benefit of intrathecal injection of insulin-like growth factor-1 in a mouse model of Amyotrophic Lateral Sclerosis

被引:79
作者
Nagano, I
Ilieva, H
Shiote, M
Murakami, T
Yokoyama, M
Shoji, M
Abe, K
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Neurol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Anesthesiol, Okayama 7008558, Japan
关键词
Akt; Bcl-2; ERK; motor neuron; SOD1; mutation; spinal cord;
D O I
10.1016/j.jns.2005.04.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Insulin-like growth factor (IGF)-1 has been shown to have a protective effect on motor neurons both in vitro, and in vivo, but has limited efficacy in patients with amyotrophic lateral sclerosis (ALS) when given subcutaneously. To examine the possible effectiveness of IGF-1 in a mouse model of familial ALS, transgenic mice expressing human: Cu/Zn superoxide dismutase (SOD1) with a G93A mutation were treated by continuous IGF-1 delivery into the intrathecal space of the lumbar spinal cord. We found that the intrathecal administration of IGF-1 improved motor performance, delayed the onset of clinical disease, and extended survival in the G93A transgenic mice. Furthermore, it increased the expression of phosphorylated Akt and ERK in spinal motor neurons, and partially prevented motor neuron loss in these mice. Taken together, the results suggest that direct administration of IGF-1 into the intrathecal space may have a therapeutic benefit for ALS. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 68
页数:8
相关论文
共 51 条
[1]  
Abe K, 1997, J NEUROSCI RES, V48, P63
[2]   INSULIN-LIKE GROWTH-FACTOR-I RECEPTORS IN HUMAN SPINAL-CORD - CHANGES IN AMYOTROPHIC-LATERAL-SCLEROSIS [J].
ADEM, A ;
EKBLOM, J ;
GILLBERG, PG ;
JOSSAN, SS ;
HOOG, A ;
WINBLAD, B ;
AQUILONIUS, SM ;
WANG, LH ;
SARA, V .
JOURNAL OF NEURAL TRANSMISSION-GENERAL SECTION, 1994, 97 (01) :73-84
[3]  
Andrus PK, 1998, J NEUROCHEM, V71, P2041
[4]   VEGF delivery with retrogradely transported lentivector prolongs survival in a mouse ALS model [J].
Azzouz, M ;
Ralph, GS ;
Storkebaum, E ;
Walmsley, LE ;
Mitrophanous, KA ;
Kingsman, SM ;
Carmeliet, P ;
Mazarakis, ND .
NATURE, 2004, 429 (6990) :413-417
[5]   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
[6]   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
[7]   SUPEROXIDE-DISMUTASE ACTIVITY, OXIDATIVE DAMAGE, AND MITOCHONDRIAL ENERGY-METABOLISM IN FAMILIAL AND SPORADIC AMYOTROPHIC-LATERAL-SCLEROSIS [J].
BOWLING, AC ;
SCHULZ, JB ;
BROWN, RH ;
BEAL, MF .
JOURNAL OF NEUROCHEMISTRY, 1993, 61 (06) :2322-2325
[8]   Involvement of protein kinase C and nitric oxide in the modulation by insulin-like growth factor-I of glutamate-induced GABA release in the cerebellum [J].
CastroAlamancos, MA ;
Arevalo, MA ;
TorresAleman, I .
NEUROSCIENCE, 1996, 70 (04) :843-847
[9]   From Charcot to Lou Gehrig: Deciphering selective motor neuron death in ALS [J].
Cleveland, DW ;
Rothstein, JD .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (11) :806-819
[10]   Preclinical testing of neuroprotective neurotrophic factors in a model of chronic motor neuron degeneration [J].
Corse, AM ;
Bilak, MM ;
Bilak, SR ;
Lehar, M ;
Rothstein, JD ;
Kuncl, RW .
NEUROBIOLOGY OF DISEASE, 1999, 6 (05) :335-346