Contrast agent-enhanced magnetic resonance imaging of skeletal muscle damage in animal models of muscular dystrophy

被引:0
作者
Straub, V
Donahue, KM
Allamand, V
Davisson, RL
Kim, YR
Campbell, KP
机构
[1] Univ Iowa, Coll Med, Howard Hughes Med Inst, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Med, Dept Neurol, Iowa City, IA 52242 USA
[3] Med Coll Wisconsin, Biophys Res Inst, Milwaukee, WI 53226 USA
[4] Univ Iowa, Coll Med, Dept Anat & Cell Biol, Iowa City, IA USA
关键词
MRI; muscular dystrophy; dystrophin; sarcoglycan;
D O I
10.1002/1522-2594(200010)44:4<655::AID-MRM22>3.3.CO;2-K
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Membrane lesions play an early role in the pathogenesis of muscular dystrophy, Using a new albumin-targeted contrast agent (MS-325), sarcolemmal integrity of two animal models for muscular dystrophy was studied by MRI, Intravenously injected MS-325 does not enter skeletal muscle of normal mice. However, mdx and Sgca-null mutant mice, animal models for Duchenne and sarcoglycan-deficient limb-girdle muscular dystrophy, respectively, showed significant accumulation of MS-325 in skeletal muscle. The results suggest that contrast agent-enhanced MRI could serve as a common, noninvasive imaging procedure for evaluating the localization, extent, and mechanisms of skeletal muscle damage in muscular dystrophy, Furthermore, this method is expected to facilitate assessment of therapeutic approaches in these diseases. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:655 / 659
页数:5
相关论文
共 33 条
[1]   HISTOPATHOLOGICAL CHANGES IN DUCHENNE MUSCULAR DYSTROPHY [J].
BELL, CD ;
CONEN, PE .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1968, 7 (03) :529-&
[2]   X-CHROMOSOME-LINKED MUSCULAR-DYSTROPHY (MDX) IN THE MOUSE [J].
BULFIELD, G ;
SILLER, WG ;
WIGHT, PAL ;
MOORE, KJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (04) :1189-1192
[3]   FACTORS IN MYOCARDIAL PERFUSION IMAGING WITH ULTRAFAST MRI AND GD-DTPA ADMINISTRATION [J].
BURSTEIN, D ;
TARATUTA, E ;
MANNING, WJ .
MAGNETIC RESONANCE IN MEDICINE, 1991, 20 (02) :299-305
[4]   DUCHENNE MUSCULAR-DYSTROPHY - PLASMA-MEMBRANE LOSS INITIATES MUSCLE-CELL NECROSIS UNLESS IT IS REPAIRED [J].
CARPENTER, S ;
KARPATI, G .
BRAIN, 1979, 102 (MAR) :147-161
[5]  
CLASEN RA, 1970, J NEUROPATH EXP NEUR, V29, P266
[6]   MUSCLE-FIBER DEGENERATION AND NECROSIS IN MUSCULAR-DYSTROPHY AND OTHER MUSCLE DISEASES - CYTOCHEMICAL AND IMMUNOCYTOCHEMICAL DATA [J].
CORNELIO, F ;
DONES, I .
ANNALS OF NEUROLOGY, 1984, 16 (06) :694-701
[7]   Progressive muscular dystrophy in α-sarcoglycan-deficient mice [J].
Duclos, F ;
Straub, V ;
Moore, SA ;
Venzke, DP ;
Hrstka, RF ;
Crosbie, RH ;
Durbeej, M ;
Lebakken, CS ;
Ettinger, AJ ;
van der Meulen, J ;
Holt, KH ;
Lim, LE ;
Sanes, JR ;
Davidson, BL ;
Faulkner, JA ;
Williamson, R ;
Campbell, KP .
JOURNAL OF CELL BIOLOGY, 1998, 142 (06) :1461-1471
[8]   alpha-sarcoglycan (adhalin) deficiency: Complete deficiency patients are 5% of childhood-onset dystrophin-normal muscular dystrophy and most partial deficiency patients do not have gene mutations [J].
Duggan, DJ ;
Fanin, M ;
Pegoraro, E ;
Angelini, C ;
Hoffman, EP .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 140 (1-2) :30-39
[9]  
Dunn JF, 1999, MUSCLE NERVE, V22, P1367, DOI 10.1002/(SICI)1097-4598(199910)22:10<1367::AID-MUS5>3.0.CO
[10]  
2-H