Clenbuterol retards loss of motor function in motor neuron degeneration mice

被引:23
作者
Zeman, RJ [1 ]
Peng, H [1 ]
Etlinger, JD [1 ]
机构
[1] New York Med Coll, Dept Cell Biol & Anat, Valhalla, NY 10595 USA
关键词
neuronal ceroid lipofuscinosis; motor neuron degeneration; eccentric nucleus; motor dysfunction; Mnd mice; clenbuterol; 2-adrenoceptor agonist;
D O I
10.1016/j.expneurol.2004.03.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Motor neuron degeneration (mnd) mice exhibit lysosomal accumulation of lipofuscin-like material that is associated with progressive loss of motor function and strength. Motor dysfunction scores at 8.5-9 months of age were highly correlated with the occurrence of abnormal spinal motor neurons with eccentric nuclei, although the total numbers of motor neurons were not significantly reduced. Nuclear eccentricity is a characteristic of the axon reaction that results from injury and subsequent compensatory axonal sprouting indicating axonal/synaptic dysfunction in mud motor neurons. Treatment with clenbuterol, a beta(2)-adrenoceptor agonist that can enhance regeneration of motor neuron axons, opposed the development of motor deficits in parallel with a reduced proportion of motor neurons with eccentric nuclei consistent with improved synaptic function. Clenbuterol also opposed decreases in grip strength and muscle mass suggesting beta(2)-agonist treatment as a potential therapeutic modality for lipofuscinoses. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:460 / 467
页数:8
相关论文
共 53 条
[1]   Ciliary neurotrophic factor activates spinal cord astrocytes, stimulating their production and release of fibroblast growth factor-2, to increase motor neuron survival [J].
Albrecht, PJ ;
Dahl, JP ;
Stoltzfus, OK ;
Levenson, R ;
Levison, SW .
EXPERIMENTAL NEUROLOGY, 2002, 173 (01) :46-62
[2]   The neuropathogenic contributions of lysosomal dysfunction [J].
Bahr, BA ;
Bendiske, J .
JOURNAL OF NEUROCHEMISTRY, 2002, 83 (03) :481-489
[3]   EFFECT OF BETA-AGONISTS ON EXPRESSION OF CALPAIN AND CALPASTATIN ACTIVITY IN SKELETAL-MUSCLE [J].
BARDSLEY, RG ;
ALLCOCK, SMJ ;
DAWSON, JM ;
DUMELOW, NW ;
HIGGINS, JA ;
LASSLETT, YV ;
LOCKLEY, AK ;
PARR, T ;
BUTTERY, PJ .
BIOCHIMIE, 1992, 74 (03) :267-273
[4]  
Baumgartner BJ, 1998, J NEUROSCI RES, V54, P766, DOI 10.1002/(SICI)1097-4547(19981215)54:6<766::AID-JNR4>3.0.CO
[5]  
2-A
[6]   Mitochondrial oxidative metabolism in motor neuron degeneration (mnd) mouse central nervous system [J].
Bertamini, M ;
Marzani, B ;
Guarneri, R ;
Guarneri, P ;
Bigini, P ;
Mennini, T ;
Curti, D .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 16 (12) :2291-2296
[7]   The development of behavioral abnormalities in the motor neuron degeneration (mnd) mouse [J].
Bolivar, VJ ;
Ganus, JS ;
Messer, A .
BRAIN RESEARCH, 2002, 937 (1-2) :74-82
[8]   Changes in synaptology of adult cat spinal α-motoneurons after axotomy [J].
Brännström, T ;
Kellerth, JO .
EXPERIMENTAL BRAIN RESEARCH, 1998, 118 (01) :1-13
[9]   MOTOR-NEURON DEGENERATION OF MICE IS A MODEL OF NEURONAL CEROID LIPOFUSCINOSIS (BATTENS DISEASE) [J].
BRONSON, RT ;
LAKE, BD ;
COOK, S ;
TAYLOR, S ;
DAVISSON, MT .
ANNALS OF NEUROLOGY, 1993, 33 (04) :381-385
[10]   NEUROFILAMENT DISTRIBUTION IS ALTERED IN THE MND (MOTOR-NEURON DEGENERATION) MOUSE [J].
CALLAHAN, LM ;
WYLEN, EL ;
MESSER, A ;
MAZURKIEWICZ, JE .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1991, 50 (04) :491-504