Suppr超能文献

低频刺激通过NMDA受体介导的蛋白磷酸酶激活来消除长时程增强。

Low-frequency stimulation erases LTP through an NMDA receptor-mediated activation of protein phosphatases.

作者信息

O'Dell T J, Kandel E R

机构信息

Howard Hughes Medical Institute,Center for Neurobiology and Behavior, College of Physicians and Surgeons of Columbia University, New York, New York 10032, USA.

出版信息

Learn Mem. 1994 Jul-Aug;1(2):129-39.

Abstract

In the CA1 region of adult guinea pig hippocampal slices, long trains of theta frequency (5 Hz) stimulation produced a small enhancement of basal synaptic transmission but depressed the strength of synaptic transmission at synapses that had recently undergone long-term potentiation (LTP). Five hertz stimulation delivered immediately prior to high-frequency stimulation also inhibited the subsequent induction of LTP. The depression of potentiated synapses by 5 Hz stimulation (depotentiation) was blocked by 2-amino-5-phosphonovalerate and was observed only during the early phases of LTP. Furthermore, the protein phosphatase inhibitors okadaic acid and calyculin A blocked both depotentiation and the ability of 5 Hz stimulation to inhibit subsequent LTP, suggesting that protein phosphatases are involved in the ability of 5 Hz stimulation to modulate synaptic plasticity in the CA1 region of the hippocampus.

摘要

在成年豚鼠海马切片的CA1区,长时间的θ频率(5赫兹)刺激会使基础突触传递略有增强,但会抑制最近经历了长时程增强(LTP)的突触处的突触传递强度。在高频刺激之前立即施加的5赫兹刺激也会抑制随后的LTP诱导。5赫兹刺激对增强突触的抑制作用(去增强)被2-氨基-5-磷酸戊酸阻断,并且仅在LTP的早期阶段观察到。此外,蛋白磷酸酶抑制剂冈田酸和花萼海绵诱癌素A既能阻断去增强作用,也能阻断5赫兹刺激抑制随后LTP的能力,这表明蛋白磷酸酶参与了5赫兹刺激调节海马CA1区突触可塑性的能力。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验