Institute for Pharmacology and Toxicology, Medical Faculty, Otto-von-Guericke University Magdeburg, 39120 Magdeburg, Germany.
Center for Behavioral Brain Sciences, Otto-von-Guericke University Magdeburg, 39106 Magdeburg, Germany.
Cells. 2021 Jan 26;10(2):238. doi: 10.3390/cells10020238.
Relief learning is the association of environmental cues with the cessation of aversive events. While there is increasing knowledge about the neural circuitry mediating relief learning, the respective molecular pathways are not known. Therefore, the aim of the present study was to examine different putative molecular pathways underlying relief learning. To this purpose, male rats were subjected either to relief conditioning or to a pseudo conditioning procedure. Forty-five minutes or 6 h after conditioning, samples of five different brain regions, namely the prefrontal cortex, nucleus accumbens (NAC), dorsal striatum, dorsal hippocampus, and amygdala, were collected. Using quantitative Western blots, the expression level of CREB, pCREB, ERK1/2, pERK1/2, CaMKIIα, MAP2K, PKA, pPKA, Akt, pAkt, DARPP-32, pDARPP-32, 14-3-3, and neuroligin2 were studied. Our analyses revealed that relief conditioned rats had higher CREB phosphorylation in NAC 6 h after conditioning than pseudo conditioned rats. The data further revealed that this CREB phosphorylation was mainly induced by dopamine D1 receptor-mediated activation of PKA, however, other kinases, downstream of the NMDA receptor, may also contribute. Taken together, the present study suggests that CREB phosphorylation, induced by a combination of different molecular pathways downstream of dopamine D1 and NMDA receptors, is essential for the acquisition and consolidation of relief learning.
缓解学习是将环境线索与厌恶事件的停止联系起来的过程。虽然人们对介导缓解学习的神经回路有了越来越多的了解,但相应的分子途径尚不清楚。因此,本研究的目的是研究缓解学习背后的不同潜在分子途径。为此,雄性大鼠接受缓解条件作用或假条件作用处理。在条件作用后 45 分钟或 6 小时,收集五个不同脑区(前额叶皮层、伏隔核(NAC)、背侧纹状体、背侧海马和杏仁核)的样本。使用定量 Western blot 技术,研究了 CREB、pCREB、ERK1/2、pERK1/2、CaMKIIα、MAP2K、PKA、pPKA、Akt、pAkt、DARPP-32、pDARPP-32、14-3-3 和神经连接蛋白 2 的表达水平。我们的分析表明,与假条件作用大鼠相比,缓解条件作用大鼠在条件作用后 6 小时 NAC 中的 CREB 磷酸化水平更高。数据进一步表明,这种 CREB 磷酸化主要是由多巴胺 D1 受体介导的 PKA 激活诱导的,但 NMDA 受体下游的其他激酶也可能有贡献。总之,本研究表明,多巴胺 D1 和 NMDA 受体下游不同分子途径共同诱导的 CREB 磷酸化对于缓解学习的获得和巩固是必不可少的。