Neurobiology of disease · 2006
Oral uridine pro-drug PN401 is neuroprotective in the R6/2 and N171-82Q mouse models of Huntington's disease.
Сравнительное исследованиеСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Saydoff Joel A, Garcia Rolando A G, Browne Susan E, Liu Liansheng, Sheng Jin, Brenneman Denise, Hu Zhongyi, Cardin Sylvain, Gonzalez Alexis, von Borstel Reid W, Gregorio Jason, Burr Holly, Beal M Flint
Аннотация
Previously, uridine pro-drug 2',3',5'-tri-O-acetyluridine (PN401) was shown to be protective in the mitochondrial complex II inhibitor 3-nitropropionic acid model of Huntington's disease (HD). In this study, PN401 increased survival and improved motor function on the rotarod in both R6/2 and N171-82Q polyglutamine repeat mouse models of HD. PN401 significantly decreased neurodegeneration in both the piriform cortex and striatum although PN401 decreased huntingtin protein aggregates only in the striatum. Cortical and striatal brain-derived neurotrophic factor (BDNF) protein levels were reduced in the +/- compared to the -/- N171-82Q mice and PN401 treatment significantly increased cortical BDNF in both +/- and -/- mice, but PN401 did not affect striatal BDNF. These results suggest that PN401 may have beneficial effects in the treatment of neurodegenerative diseases such as HD.
Предметные рубрики MeSH
AcetatesAdministration, OralAnalysis of VarianceAnimalsCerebral CortexDisease Models, AnimalFemaleHuntingtin ProteinHuntington DiseaseMaleMiceMice, Inbred C3HMice, Inbred C57BLMice, Neurologic MutantsMice, TransgenicMotor ActivityNeostriatumNerve DegenerationNerve Tissue ProteinsNeuroprotective AgentsNuclear ProteinsProdrugsRotarod Performance TestUridine