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The novel estrogen receptor modulator STX attenuates Amyloid-ß neurotoxicity in the 5XFAD mouse model of Alzheimer's disease.
Quinn, Joseph F; Kelly, Martin J; Harris, Christopher J; Hack, Wyatt; Gray, Nora E; Kulik, Veronika; Bostick, Zoe; Brumbach, Barbara H; Copenhaver, Philip F.
Afiliación
  • Quinn JF; Department of Neurology, Oregon Health and Science University, Portland, OR, United States of America; Parkinson's Disease Research, Education, and Clinical Center, Portland Veterans Affairs Medical Center, Portland, OR, United States of America. Electronic address: quinnj@ohsu.edu.
  • Kelly MJ; Department of Chemical Physiology and Biochemistry, OHSU, Portland, OR, United States of America.
  • Harris CJ; Department of Neurology, Oregon Health and Science University, Portland, OR, United States of America.
  • Hack W; Department of Neurology, Oregon Health and Science University, Portland, OR, United States of America.
  • Gray NE; Department of Neurology, Oregon Health and Science University, Portland, OR, United States of America.
  • Kulik V; Department of Neurology, Oregon Health and Science University, Portland, OR, United States of America.
  • Bostick Z; Department of Cell, Developmental and Cancer Biology, OHSU, Portland, OR, United States of America.
  • Brumbach BH; Biostatistics and Design Program, OHSU-PSU School of Public Health, Portland, OR, United States of America.
  • Copenhaver PF; Department of Cell, Developmental and Cancer Biology, OHSU, Portland, OR, United States of America.
Neurobiol Dis ; 174: 105888, 2022 Nov.
Article en En | MEDLINE | ID: mdl-36209948
ABSTRACT
Based on previous evidence that the non-steroidal estrogen receptor modulator STX mitigates the effects of neurotoxic Amyloid-ß (Aß) in vitro, we have evaluated its neuroprotective benefits in a mouse model of Alzheimer's disease. Cohorts of 5XFAD mice, which begin to accumulate cerebral Aß at two months of age, were treated with orally-administered STX starting at 6 months of age for two months. After behavioral testing to evaluate cognitive function, biochemical and immunohistochemical assays were used to analyze key markers of mitochondrial function and synaptic integrity. Oral STX treatment attenuated Aß-associated mitochondrial toxicity and synaptic toxicity in the brain, as previously documented in cultured neurons. STX also moderately improved spatial memory in 5XFAD mice. In addition, STX reduced markers for reactive astrocytosis and microgliosis surrounding amyloid plaques, and also unexpectedly reduced overall levels of cerebral Aß in the brain. The neuroprotective effects of STX were more robust in females than in males. These results suggest that STX may have therapeutic potential in Alzheimer's Disease.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Neurotoxicidad / Enfermedad de Alzheimer Límite: Animals Idioma: En Revista: Neurobiol Dis Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes de Neurotoxicidad / Enfermedad de Alzheimer Límite: Animals Idioma: En Revista: Neurobiol Dis Asunto de la revista: NEUROLOGIA Año: 2022 Tipo del documento: Article