Metformin therapy in a transgenic mouse model of Huntington's disease

被引:185
作者
Ma, Thong C. [1 ]
Buescher, Jessica L. [1 ]
Oatis, Benjamin [1 ]
Funk, Jason A. [1 ]
Nash, Andrew J. [1 ]
Carrier, Raeann L. [1 ]
Hoyt, Kari R. [1 ]
机构
[1] Ohio State Univ, Div Pharmacol, Columbus, OH 43210 USA
关键词
metformin; dimethylbiguanide; biguanides; Huntington's disease; huntingtin; neurodegeneration; ACTIVATED PROTEIN-KINASE; RESPIRATORY-CHAIN; SKELETAL-MUSCLE; H-1-NMR SPECTROSCOPY; GLUCOSE-PRODUCTION; DIABETES-MELLITUS; ENERGY-METABOLISM; MOTOR DEFICITS; CAG REPEAT; IN-VIVO;
D O I
10.1016/j.neulet.2006.10.039
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Huntington's disease (HD) is a hereditary neurodegenerative disease that leads to striatal degeneration and a severe movement disorder. We used a transgenic mouse model of HD (the R6/2 line with similar to 150 glutamine repeats) to test a new therapy for this disease. We treated HD mice with metformin, a widely used anti-diabetes drug, in the drinking water (0, 2 or 5 mg/ml) starting at 5 weeks of age. Metformin treatment significantly prolonged the survival time of male HD mice at the 2 mg/ml dose (20.1% increase in lifespan) without affecting fasting blood glucose levels. This dose of metformin also decreased hind limb clasping time in 11-week-old mice. The higher dose did not prolong survival, and neither dose of metformin was effective in female HD mice. Collectively, our results suggest that metformin may be worth further investigation in additional HD models. (c) 2006 Published by Elsevier Ireland Ltd.
引用
收藏
页码:98 / 103
页数:6
相关论文
共 43 条
[1]   Huntington's disease of the endocrine pancreas: Insulin deficiency and diabetes mellitus due to impaired insulin gene expression [J].
Andreassen, OA ;
Dedeoglu, A ;
Stanojevic, V ;
Hughes, DB ;
Browne, SE ;
Leech, CA ;
Ferrante, RJ ;
Habener, JF ;
Beal, MF ;
Thomas, MK .
NEUROBIOLOGY OF DISEASE, 2002, 11 (03) :410-424
[2]  
Beckmann R., 1971, HDB EXPTL PHARMAKOLO, P439, DOI [10.1007/978-3-642-65265-3_8, DOI 10.1007/978-3-642-65265-3_8]
[3]   Oxidative damage and metabolic dysfunction in Huntington's disease: Selective vulnerability of the basal ganglia [J].
Browne, SE ;
Bowling, AC ;
MacGarvey, U ;
Baik, MJ ;
Berger, SC ;
Muqit, MMK ;
Bird, ED ;
Beal, MF .
ANNALS OF NEUROLOGY, 1997, 41 (05) :646-653
[4]   The energetics of Huntington's disease [J].
Browne, SE ;
Beal, MF .
NEUROCHEMICAL RESEARCH, 2004, 29 (03) :531-546
[5]   Age-dependent changes in the calcium sensitivity of striatal mitochondria in mouse models of Huntington's disease [J].
Brustovetsky, N ;
LaFrance, R ;
Purl, KJ ;
Brustovetsky, T ;
Keene, CD ;
Low, WC ;
Dubinsky, JM .
JOURNAL OF NEUROCHEMISTRY, 2005, 93 (06) :1361-1370
[6]  
Carter RJ, 1999, J NEUROSCI, V19, P3248
[7]   Creatine therapy provides neuroprotection after onset of clinical symptoms in Huntington's disease transgenic mice [J].
Dedeoglu, A ;
Kubilus, JK ;
Yang, LC ;
Ferrante, KL ;
Hersch, SM ;
Beal, MF ;
Ferrante, RJ .
JOURNAL OF NEUROCHEMISTRY, 2003, 85 (06) :1359-1367
[8]   Obligatory role of membrane events in the regulatory effect of metformin on the respiratory chain function [J].
Detaille, D ;
Guigas, B ;
Leverve, X ;
Wiernsperger, N ;
Devos, P .
BIOCHEMICAL PHARMACOLOGY, 2002, 63 (07) :1259-1272
[9]   Therapeutic effects of metformin on insulin resistance and hyperandrogenism in polycystic ovary syndrome [J].
Diamanti-Kandarakis, E ;
Kouli, C ;
Tsianateli, T ;
Bergiele, A .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1998, 138 (03) :269-274
[10]   Weight loss in early stage of Huntington's disease [J].
Djoussé, L ;
Knowlton, B ;
Cupples, LA ;
Marder, K ;
Shoulson, I ;
Myers, RH .
NEUROLOGY, 2002, 59 (09) :1325-1330