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Combined treatment with valproic acid and estrogen has neuroprotective effects in ovariectomized mice with Alzheimer's disease.
Li, Yan-Zhen; Liu, Yuan-Jie; Zhang, Wei; Luo, Shi-Fang; Zhou, Xin; He, Gui-Qiong.
Afiliación
  • Li YZ; Chongqing Key Laboratory of Neurobiology, Chongqing Medical University, Chongqing, China.
  • Liu YJ; Chongqing Key Laboratory of Neurobiology; Department of Anatomy, Chongqing Medical University, Chongqing, China.
  • Zhang W; Chongqing Key Laboratory of Neurobiology, Chongqing Medical University, Chongqing, China.
  • Luo SF; Chongqing Key Laboratory of Neurobiology; Department of Anatomy, Chongqing Medical University, Chongqing, China.
  • Zhou X; Department of Galactophore, Chongqing University Cancer Hospital, Chongqing, China.
  • He GQ; Chongqing Key Laboratory of Neurobiology; Department of Anatomy, Chongqing Medical University, Chongqing, China.
Neural Regen Res ; 16(10): 2078-2085, 2021 Oct.
Article en En | MEDLINE | ID: mdl-33642397
ABSTRACT
Postmenopausal women with Alzheimer's disease (AD) exhibit dramatically reduced sensitivity to estrogen replacement therapy, which is though to be related to an estrogen receptor (ER)α/ERß ratio imbalance arising from a significantly decreased level of ERs of the brain. The aim of our study was to investigate whether valproic acid (VPA) can enhance the beneficial effects of estrogen on cognitive function through restoration of ERα and ERß expression in the brain. We removed the ovaries of female APP/PS1 mice to simulate the low estrogen levels present in postmenopausal women and then administered VPA (30 mg/kg, intraperitoneal injection, once daily), 17ß-estradiol (E2) (2.4 µg, intraperitoneal injection, once daily), liquiritigenin (LG) (50 µg/kg, intragastric infusion, once daily), VPA + E2, or VPA + LG for 4 successive weeks. Compared with treatment with a single drug, treatment with VPA + E2 or VPA + LG significantly increased the level of glycogen synthase kinase 3ß, increased the expression of estrogen receptor α, reduced the expression of small ubiquitin-like modifiers, and increased the level of estrogen receptor ß. This resulted in enhanced sensitivity to estrogen therapy, reduced amyloid ß aggregation, reduced abnormal phosphorylation of the tau protein, reduced neuronal loss, increased dendritic spine and postsynaptic density, and significantly alleviated memory loss and learning impairment in mice. This study was approved by the Chongqing Medical University Animal Protection and Ethics Committee, China on March 6, 2013.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Ethics Idioma: En Revista: Neural Regen Res Año: 2021 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Aspecto: Ethics Idioma: En Revista: Neural Regen Res Año: 2021 Tipo del documento: Article País de afiliación: China