6533b830fe1ef96bd12978dc
RESEARCH PRODUCT
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subject
Genetically modified mousemedicine.medical_specialtyPathologyProteolipid protein 1TransgeneMicrogliosis03 medical and health scienceschemistry.chemical_compound0302 clinical medicineInternal medicinemedicine030304 developmental biology0303 health sciencesbusiness.industryGeneral NeuroscienceLeukodystrophyPelizaeus–Merzbacher diseaseGlutathionemedicine.disease3. Good healthEndocrinologychemistryCurcuminNeurology (clinical)business030217 neurology & neurosurgerydescription
Objective Pelizaeus–Merzbacher disease (PMD) is a progressive and lethal leukodystrophy caused by mutations affecting the proteolipid protein (PLP1) gene. The most common cause of PMD is a duplication of PLP1 and at present there is no curative therapy available. Methods By using transgenic mice carrying additional copies of Plp1, we investigated whether curcumin diet ameliorates PMD symptoms. The diet of Plp1 transgenic mice was supplemented with curcumin for 10 consecutive weeks followed by phenotypical, histological and immunohistochemical analyses of the central nervous system. Plp1 transgenic and wild-type mice fed with normal chow served as controls. Results Curcumin improved the motor phenotype performance of Plp1 transgenic mice by 50% toward wild-type level and preserved myelinated axons by 35% when compared to Plp1 transgenic controls. Furthermore, curcumin reduced astrocytosis, microgliosis and lymphocyte infiltration in Plp1 transgenic mice. Curcumin diet did not affect the pathologically increased Plp1 mRNA abundance. However, high glutathione levels indicating an oxidative misbalance in the white matter of Plp1 transgenic mice were restored by curcumin treatment. Interpretation Curcumin may potentially serve as an antioxidant therapy of PMD caused by PLP1 gene duplication.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2015-06-24 | Annals of Clinical and Translational Neurology |