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Hum Mol Genet ; 25(9): 1792-802, 2016 05 01.
Article in English | MEDLINE | ID: mdl-26908614

ABSTRACT

Oxidative damage to mitochondria (MT) is a major mechanism for aging and neurodegeneration. We have developed a novel synthetic antioxidant, XJB-5-131, which directly targets MT, the primary site and primary target of oxidative damage. XJB-5-131 prevents the onset of motor decline in an HdhQ(150/150) mouse model for Huntington's disease (HD) if treatment starts early. Here, we report that XJB-5-131 attenuates or reverses disease progression if treatment occurs after disease onset. In animals with well-developed pathology, XJB-5-131 promotes weight gain, prevents neuronal death, reduces oxidative damage in neurons, suppresses the decline of motor performance or improves it, and reduces a graying phenotype in treated HdhQ(150/150) animals relative to matched littermate controls. XJB-5-131 holds promise as a clinical candidate for the treatment of HD.


Subject(s)
Cyclic N-Oxides/pharmacology , Disease Models, Animal , Huntington Disease/drug therapy , Mitochondria/drug effects , Motor Activity/drug effects , Oxidative Stress/drug effects , Animals , Behavior, Animal/drug effects , Cells, Cultured , Huntington Disease/metabolism , Huntington Disease/physiopathology , Mice , Mice, Inbred C57BL , Mitochondria/metabolism , Mitochondria/pathology , Neurons/cytology , Neurons/drug effects , Neurons/metabolism , Weight Loss/drug effects
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