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Combined treatment with valproic acid and estrogen has neuroprotective effects in ovariectomized mice with Alzheimer’s disease

机译:用阿尔茨海默病的卵巢切除小鼠在卵巢切除小鼠中具有神经保护作用

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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/ERβ 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 ERβ 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), 17β-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 3β, increased the expression of estrogen receptor α, reduced the expression of small ubiquitin-like modifiers, and increased the level of estrogen receptor β. This resulted in enhanced sensitivity to estrogen therapy, reduced amyloid β 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.
机译:具有阿尔茨海默病(AD)的绝经后妇女(AD)表现出对雌激素替代疗法的敏感性显着降低,但是与雌激素受体(ER)α/ERβ比率不平衡有关,其脑卒中的雌激素受体(ER)α/ERβ比率不平衡。我们研究的目的是探讨丙甲酸(VPA)是否可以通过恢复脑中的ERα和ERβ表达来增强雌激素对认知功能的有益作用。我们取下了女性APP / PS1小鼠的卵巢,以模拟绝经后女性中存在的低雌激素水平,然后施用VPA(30mg / kg,腹膜内注射,每日一次),17β-雌二醇(E2)(2.4μg,腹膜内注射,每日一次),液中素(LG)(50μg/ kg,胃内输注,每日一次),VPA E2或VPA LG连续4周。与单一药物的处理相比,用VPA E2或VPA Lg处理显着增加了糖原合酶激酶3β的水平,增加了雌激素受体α的表达,降低了小泛素样改性剂的表达,并增加了雌激素受体的水平β这导致增强对雌激素治疗的敏感性,降低淀粉样蛋白β聚集,降低Tau蛋白的异常磷酸化,降低神经元损失,增加的树突脊柱和突触后密度,并显着缓解了小鼠中的记忆丧失和学习损伤。 2013年3月6日重庆医科大学动物保护和伦理委员会批准了这项研究。

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