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丝裂原活化蛋白激酶/细胞外信号调节激酶信号通路的激活导致环磷酸腺苷反应元件结合蛋白磷酸化,这是幼鼠厌恶嗅觉学习长期易化过程所必需的。

Activation of the mitogen-activated protein kinase/extracellular signal-regulated kinase signaling pathway leading to cyclic AMP response element-binding protein phosphorylation is required for the long-term facilitation process of aversive olfactory learning in young rats.

作者信息

Zhang J-J, Okutani F, Inoue S, Kaba H

机构信息

Department of Neuropsychiatry, Kochi Medical School, Nankoku, Kochi 783-8505, Japan.

出版信息

Neuroscience. 2003;121(1):9-16. doi: 10.1016/s0306-4522(03)00392-0.

Abstract

The mitogen-activated protein kinase/extracellular-signal regulated kinase (MAPK/ERK) cascade is an important contributor to synaptic plasticity that underlies learning and memory. ERK activation by the MAPK/ERK kinase (MEK) leading to cyclic-AMP response element binding protein (CREB) phosphorylation is implicated in the formation of long-term memory. We have demonstrated that CREB phosphorylation in the olfactory bulb (OB) is important for aversive olfactory learning in young rats, yet whether MAPK/ERK functions as an upstream regulator are necessary for this olfactory learning remains to be determined. Therefore, we addressed this issue using behavioral and Western blot analyses. The MEK inhibitor PD98059 was continuously infused into the OB of postnatal day 11 rat pups during a 30-min training session regarding the pairing of citral odor and foot shock. On the following day, the time spent in the part of the apparatus where the odor was present was measured as an index of odor aversion. PD98059 impaired olfactory learning in a dose-dependent manner without affecting memory retention 1 h after training. We further tested whether odor-shock training leads to MAPK/ERK activation in the OB and defines the time course of the activation. Phosphorylated ERKs (P-ERKs) 1 and 2 were significantly increased for 60 min after the training without changes in total ERKs 1 and 2. By contrast, intrabulbar infusion of PD98059 during the training significantly reduced P-ERKs 1 and 2 as well as phosphorylated CREB without any effects on the total ERKs or CREB. Taken together with the previous findings, these results indicate that the MAPK/ERK-CREB pathway is required for the long-term, but not the short-term, facilitation process of aversive olfactory learning in young rats.

摘要

丝裂原活化蛋白激酶/细胞外信号调节激酶(MAPK/ERK)级联反应是突触可塑性的重要促成因素,而突触可塑性是学习和记忆的基础。MAPK/ERK激酶(MEK)激活ERK导致环磷酸腺苷反应元件结合蛋白(CREB)磷酸化,这与长期记忆的形成有关。我们已经证明,嗅球(OB)中的CREB磷酸化对幼鼠的厌恶嗅觉学习很重要,但MAPK/ERK作为上游调节因子对这种嗅觉学习是否必要仍有待确定。因此,我们使用行为学和蛋白质免疫印迹分析来解决这个问题。在对柠檬醛气味和足部电击进行配对的30分钟训练期间,将MEK抑制剂PD98059持续注入出生后第11天的幼鼠的嗅球中。在接下来的一天,测量在有气味的装置部分所花费的时间,作为气味厌恶的指标。PD98059以剂量依赖性方式损害嗅觉学习,而不影响训练后1小时的记忆保持。我们进一步测试了气味-电击训练是否会导致嗅球中MAPK/ERK激活,并确定激活的时间进程。训练后60分钟,磷酸化ERK1和ERK2显著增加,而总ERK1和ERK2没有变化。相比之下,训练期间球内注入PD98059显著降低了磷酸化ERK1和ERK2以及磷酸化CREB,而对总ERK或CREB没有任何影响。结合先前的研究结果,这些结果表明,MAPK/ERK-CREB通路是幼鼠厌恶嗅觉学习的长期促进过程所必需的,但不是短期促进过程所必需的。

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