Pre-clinical screening of drugs using the mdx mouse

被引:119
作者
Granchelli, JA [1 ]
Pollina, C [1 ]
Hudecki, MS [1 ]
机构
[1] SUNY Buffalo, Dept Biol Sci, Buffalo, NY 14260 USA
关键词
mds; mouse; muscular dystrophy; therapy; therapeutic evaluation;
D O I
10.1016/S0960-8966(99)00126-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The genetically dystrophin-deficient mdx mouse, with its characteristic and regular exercise-induced loss of strength, is a useful experimental platform on which to screen potential drug therapies in the treatment of some dystrophic diseases. Pharmacological agents of several chemical and functional classes were examined in their ability to reduce the loss of muscular strength in young exercised mdx mice. Therapeutic intervention over the period 4-10 weeks of age was evaluated in weekly tests of whole-body strength. This age period represents the most severe manifestation of disease in these animals. Significant improvements in whole-body strength were brought about by treatment with the immunosuppressive and anti-inflammatory drugs prednisone (at low dose only, 1 mg/kg body weight), pentoxifylline (100 mg/kg) and tinset (100 mg/kg). The anabolic hormone insulin-like growth factor-1 (5 mg/kg), as well as the amino acids/metabolites glutamine (10 mg/kg), glutamine plus alanine (each 10 mg/kg), and creatinine (10 mg/kg) all improved strength test performance. The mdx mouse is a responsive system for the screening of potential therapeutic treatments for the muscular dystrophies. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:235 / 239
页数:5
相关论文
共 32 条
[1]  
BALOH R, 1972, LAB INVEST, V26, P319
[2]   HUMAN MUSCULAR DYSTROPHY AS AN ABERRATION OF THE CONNECTIVE TISSUE [J].
BOURNE, GH ;
GOLARZ, MN .
NATURE, 1959, 183 (4677) :1741-1743
[3]   CLINICAL INVESTIGATION OF DUCHENNE MUSCULAR-DYSTROPHY - INTERESTING RESULTS IN A TRIAL OF PREDNISONE [J].
BROOKE, MH ;
FENICHEL, GM ;
GRIGGS, RC ;
MENDELL, JR ;
MOXLEY, RT ;
MILLER, JP ;
KAISER, KK ;
FLORENCE, JM ;
PANDYA, S ;
SIGNORE, L ;
KING, W ;
ROBISON, J ;
HEAD, RA ;
PROVINCE, MA ;
SEYFRIED, W ;
MANDEL, S .
ARCHIVES OF NEUROLOGY, 1987, 44 (08) :812-817
[5]  
COOPER BJ, 1989, BR MED B, V45, P713
[6]   THE MDX MOUSE SKELETAL-MUSCLE MYOPATHY .1. A HISTOLOGICAL, MORPHOMETRIC AND BIOCHEMICAL INVESTIGATION [J].
COULTON, GR ;
MORGAN, JE ;
PARTRIDGE, TA ;
SLOPER, JC .
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1988, 14 (01) :53-70
[7]   ELEVATED BASIC FIBROBLAST GROWTH-FACTOR IN THE SERUM OF PATIENTS WITH DUCHENNE MUSCULAR-DYSTROPHY [J].
DAMORE, PA ;
BROWN, RH ;
KU, PT ;
HOFFMAN, EP ;
WATANABE, H ;
ARAHATA, K ;
ISHIHARA, T ;
FOLKMAN, J .
ANNALS OF NEUROLOGY, 1994, 35 (03) :362-365
[8]   PREDNISONE TREATMENT IN DUCHENNE MUSCULAR-DYSTROPHY - LONG-TERM BENEFIT [J].
DESILVA, S ;
DRACHMAN, DB ;
MELLITS, D ;
KUNCL, RW .
ARCHIVES OF NEUROLOGY, 1987, 44 (08) :818-822
[9]  
DRACHMAN DB, 1974, LANCET, V2, P1409
[10]   A ROLE FOR COLLAGEN IN THE PATHOGENESIS OF MUSCULAR-DYSTROPHY [J].
DUANCE, VC ;
STEPHENS, HR ;
DUNN, M ;
BAILEY, AJ ;
DUBOWITZ, V .
NATURE, 1980, 284 (5755) :470-472