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首页> 外文期刊>Neurochemical Research >Altered Postsynaptic-Density-Levels of Caldendrin in the Para-Chloroamphetamine-Induced Serotonin Syndrome but not in the Rat Ketamine Model of Psychosis
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Altered Postsynaptic-Density-Levels of Caldendrin in the Para-Chloroamphetamine-Induced Serotonin Syndrome but not in the Rat Ketamine Model of Psychosis

机译:在对氯苯丙胺诱导的5-羟色胺综合征中改变了Caldendrin的突触后密度水平,但在大鼠氯胺酮精神病模型中却没有改变。

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摘要

Caldendrin is a synaptic calcium sensor protein that is tightly associated with the postsynaptic density (PSD). Previous work has shown that the association of the protein with the synapse is highly dynamic and is increased in an activity-dependent manner. In the present study the caldendrin-association with the postsynaptic cytomatrix was analyzed in animal models of psychosis and drug abuse induced neurotoxicity. Subchronic administration of the N-methyl-d-aspartate (NMDA)-receptor antagonist ketamine, serving as a model of NMDA-receptor hypofunction and schizophrenia showed no significant effect on the PSD-levels of caldendrin, indicating that NMDA-receptor activity is not required to keep caldendrin at the synapse. However, administration of high doses of the serotonergic neurotoxin p-chloroamphetamine (PCA) lead to significant changes in the association of caldendrin with the PSD. These results underscore the dynamic association of caldendrin with the PSD and suggest a role of this synaptic calcium sensor in the PCA-induced serotonin syndrome.
机译:Caldendrin是一种突触钙传感器蛋白,与突触后密度(PSD)紧密相关。先前的工作表明蛋白质与突触的缔合是高度动态的,并且以活性依赖性方式增加。在本研究中,在精神病和药物滥用引起的神经毒性动物模型中分析了钙调蛋白与突触后细胞基质的联系。 N-甲基-d-天冬氨酸(NMDA)受体拮抗剂氯胺酮的亚慢性给药,作为NMDA受体功能低下和精神分裂症的模型,对Caldendrin的PSD水平没有显着影响,表明NMDA受体活性不高要求将降钙素保留在突触中。但是,高剂量的血清素能神经毒素对氯苯丙胺(PCA)的使用会导致Caldendrin与PSD的结合发生重大变化。这些结果强调了Caldendrin与PSD的动态联系,并暗示了这种突触钙传感器在PCA诱导的5-羟色胺综合征中的作用。

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