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首页> 外文期刊>Neurochemical Research >Neuroprotective Potential of Biphalin, Multireceptor Opioid Peptide, Against Excitotoxic Injury in Hippocampal Organotypic Culture
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Neuroprotective Potential of Biphalin, Multireceptor Opioid Peptide, Against Excitotoxic Injury in Hippocampal Organotypic Culture

机译:Biphalin,多受体阿片肽对海马器官型培养中兴奋性毒性损伤的神经保护潜力。

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摘要

Biphalin is a dimeric opioid peptide that exhibits affinity for three types of opioid receptors (MOP, DOP and KOP). Biphalin is undergoing intensive preclinical study. It was recognized that activation of δ-opioid receptor elicits neuroprotection against brain hypoxia and ischemia. We compare the effect of biphalin and morphine and the inhibition of opioid receptors by naltrexone on survival of neurons in rat organotypic hippocampal cultures challenged with NMDA. Findings: (1) 0.025–0.1 μM biphalin reduces NMDA-induced neuronal damage; (2) biphalin neuroprotection is abolished by naltrexone; (3) reduced number of dead cells is shown even if biphalin is applied with delay after NMDA challenge.
机译:Biphalin是一种二聚体类阿片肽,对三种类型的阿片受体(MOP,DOP和KOP)具有亲和力。 Biphalin正在接受深入的临床前研究。已经认识到,δ-阿片样物质受体的激活引起针对脑缺氧和局部缺血的神经保护。我们比较了双萘酚和吗啡的作用以及纳曲酮对阿片受体的抑制作用对受NMDA攻击的大鼠器官型海马培养神经元存活的影响。结果:(1)0.025–0.1μMBiphalin减少NMDA诱导的神经元损伤; (2)纳曲酮废除了双相蛋白的神经保护作用; (3)即使在NMDA攻击后延迟应用了Biphalin,死细胞的数量也会减少。

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