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首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >The antidepressant action of 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid is mediated by phosphorylation of histone deacetylase 5
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The antidepressant action of 3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid is mediated by phosphorylation of histone deacetylase 5

机译:组蛋白脱乙酰基酶5的磷酸化介导了3-(2-羧基哌嗪-4-基)丙基-1-膦酸的抗抑郁作用

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摘要

3-(2-Carboxypiperazin-4-yl)propyl-1-phosphonic acid (CPP), a competitive N-methyl-D-aspartate (NMDA) receptor antagonist, produces rapid antidepressant-like effects in animal models of depression. However, the molecular mechanisms underlying these behavioral actions remain unknown. Here, we demonstrate that CPP rapidly stimulates histone deacetylase (HDAC) 5 phosphorylation and nuclear export in rat hippocampal neurons. These effects are accompanied by calcium/calmodulin kinase II (CaMKII) and protein kinase D (PKD) phosphorylation. Behavioral experiments revealed that viral-mediated hippocampal knockdown of HDAC5 blocked the antidepressant effects of CPP in stressed animals. Taken together, our results imply that CPP acts via HDAC5 and suggest that HDAC5 is a common regulator contributing to the antidepressant actions of NMDA receptor antagonists such as CPP.
机译:3-(2-羧基哌嗪-4-基)丙基-1-膦酸(CPP)是一种竞争性N-甲基-D-天冬氨酸(NMDA)受体拮抗剂,在抑郁动物模型中产生快速的抗抑郁样作用。但是,这些行为的潜在分子机制仍然未知。在这里,我们证明了CPP会迅速刺激大鼠海马神经元中的组蛋白脱乙酰基酶(HDAC)5磷酸化和核输出。这些作用伴有钙/钙调蛋白激酶II(CaMKII)和蛋白激酶D(PKD)磷酸化。行为实验表明,HDAC5的病毒介导的海马敲除作用阻断了CPP对应激动物的抗抑郁作用。综上所述,我们的结果暗示CPP通过HDAC5起作用,并暗示HDAC5是有助于NMDA受体拮抗剂(如CPP)的抗抑郁作用的常见调节剂。

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