Human Molecular Genetics · 2016 · 59 citations · 38 references
Life SciencesNeurobiologyNeuroscienceMitochondrial BiologyNeurobiology Of DiseaseNeurodegenerationHuntington DiseaseMitochondrial DysfunctionMitochondrial Function In NeuronsNeurodegeneration MechanismsNeurodegenerative DiseasesNeurodegenerative DisordersHuntington Disease NeuroprotectionMitochondrial Antioxidant DefenseMitochondrial Dysfunction TherapeuticsMitochondrial Oxidative StressMitochondrial Toxicity MechanismsMotor PerformanceOxidative Stress In Neurodegeneration
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.
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NIH Image to ImageJ: 25 years of image analysis
Caroline A Schneider, Wayne Rasband, Kevin W. Eliceiri · Nature Methods · 2012 · 65.2K citations