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Adiponectin protects rat hippocampal neurons against excitotoxicity

机译:脂联素保护大鼠海马神经元免受兴奋性毒性

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摘要

Adiponectin exerts multiple regulatory functions in the body and in the hypothalamus primarily through activation of its two receptors, adiponectin receptor1 and adiponectin receptor 2. Recent studies have shown that adiponectin receptors are widely expressed in other areas of the brain including the hippocampus. However, the functions of adiponectin in brain regions other than the hypothalamus are not clear. Here, we report that adiponectin can protect cultured hippocampal neurons against kainic acid-induced (KA) cytotoxicity. Adiponectin reduced the level of reactive oxygen species, attenuated apoptotic cell death, and also suppressed activation of caspase-3 induced by KA. Pretreatment of hippocampal primary neurons with an AMPK inhibitor, compound C, abolished adiponectin-induced neuronal protection. The AMPK activator, 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside, attenuated KA-induced caspase-3 activity. These findings suggest that the AMPK pathway is critically involved in adiponectin-induced neuroprotection and may mediate the antioxidative and anti-apoptotic properties of adiponectin.
机译:脂联素主要通过其两个受体脂联素受体1和脂联素受体2的激活而在体内和下丘脑中发挥多种调节功能。最近的研究表明,脂联素受体在包括海马在内的大脑其他区域广泛表达。但是,脂联素在除下丘脑以外的脑区域中的功能尚不清楚。在这里,我们报告脂联素可以保护培养的海马神经元免受海藻酸诱导的(KA)细胞毒性。脂联素降低了活性氧的水平,减轻了凋亡细胞的死亡,并且还抑制了由KA诱导的caspase-3的活化。用AMPK抑制剂化合物C预处理海马原代神经元可消除脂联素诱导的神经元保护作用。 AMPK激活剂5-氨基咪唑-4-羧酰胺-1-β-D-核呋喃糖苷减弱了KA诱导的caspase-3活性。这些发现表明,AMPK途径与脂联素诱导的神经保护作用密切相关,并可能介导脂联素的抗氧化和抗凋亡特性。

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