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对大鼠长期给予N-甲基-D-天冬氨酸(NMDA)可上调额叶皮质胞质磷脂酶A2及其转录因子激活蛋白2。

Chronic NMDA administration to rats up-regulates frontal cortex cytosolic phospholipase A2 and its transcription factor, activator protein-2.

作者信息

Rao Jagadeesh S, Ertley Renee N, Rapoport Stanley I, Bazinet Richard P, Lee Ho-Joo

机构信息

Brain Physiology and Metabolism Section, National Institute on Aging, National Institutes of Health, Bethesda, Maryland, USADepartment of Nutritional Sciences, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

出版信息

J Neurochem. 2007 Sep;102(6):1918-1927. doi: 10.1111/j.1471-4159.2007.04648.x. Epub 2007 May 10.

Abstract

Excessive N-methyl-D-aspartate (NMDA) signaling is thought to contribute to bipolar disorder symptoms. Lithium and carbamazepine, effective against bipolar mania, are reported in rats to reduce brain transcription of an arachidonic acid selective calcium-dependent cytosolic phospholipase A(2) (cPLA(2)), as well as expression of one of its transcription factors, activator protein (AP)-2. In this study, we determined if chronic administration of NMDA (25 mg/kg i.p.) to rats would increase brain cPLA(2) and AP-2 expression, as these antimanic drugs are known to down-regulate excessive NMDA signaling. Administration of a daily subconvulsive dose of NMDA to rats for 21 days decreased frontal cortex NMDA receptor (NR)-1 and NR-3A subunits and increased cPLA(2) activity, phosphorylation, protein, and mRNA levels. The activity and protein levels of secretory phospholipase A(2) or calcium-independent phospholipase A(2) were not changed significantly. Chronic NMDA also increased the DNA-binding activity of AP-2 and the protein levels of its alpha and beta subunits. These changes were absent following acute (3 h earlier) NMDA administration. The changes, opposite to those found following chronic lithium or carbamazepine, are consistent with up-regulated arachidonic acid release due to excessive NR signaling and may be a contributing factor to bipolar mania.

摘要

过量的N-甲基-D-天冬氨酸(NMDA)信号传导被认为与双相情感障碍症状有关。据报道,对大鼠有效的抗双相躁狂症药物锂盐和卡马西平可降低花生四烯酸选择性钙依赖性胞质磷脂酶A2(cPLA2)的脑转录水平,以及其转录因子之一激活蛋白(AP)-2的表达。在本研究中,我们确定了对大鼠长期给予NMDA(25mg/kg腹腔注射)是否会增加脑cPLA2和AP-2的表达,因为已知这些抗躁狂药物可下调过量的NMDA信号传导。对大鼠每日给予亚惊厥剂量的NMDA,持续21天,可降低额叶皮质NMDA受体(NR)-1和NR-3A亚基水平,并增加cPLA2活性、磷酸化水平、蛋白水平和mRNA水平。分泌型磷脂酶A2或钙非依赖性磷脂酶A2的活性和蛋白水平没有显著变化。长期给予NMDA还可增加AP-2的DNA结合活性及其α和β亚基的蛋白水平。急性(提前3小时)给予NMDA后未出现这些变化。这些与长期给予锂盐或卡马西平后发现的变化相反,与过量NR信号传导导致的花生四烯酸释放上调一致,可能是双相躁狂症的一个促成因素。

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