GABAB Receptor Activation Inhibits Neuronal Excitability and Spatial Learning in the Entorhinal Cortex by Activating TREK-2 K+ Channels

被引:103
|
作者
Deng, Pan-Yue [1 ]
Xiao, Zhaoyang [1 ]
Yang, Chuanxiu [1 ]
Rojanathammanee, Lalida [1 ]
Grisanti, Laurel [1 ]
Watt, John [2 ]
Geiger, Jonathan D. [1 ]
Liu, Rugao [2 ]
Porter, James E. [1 ]
Lei, Saobo [1 ]
机构
[1] Univ N Dakota, Sch Med & Hlth Sci, Dept Pharmacol Physiol & Therapeut, Grand Forks, ND 58203 USA
[2] Univ N Dakota, Sch Med & Hlth Sci, Dept Anat & Cell Biol, Grand Forks, ND 58203 USA
关键词
BACKGROUND POTASSIUM CHANNELS; MEDIAL TEMPORAL-LOBE; CEREBELLAR GRANULE NEURONS; PROTEIN-COUPLED RECEPTORS; ARACHIDONIC-ACID; PARAHIPPOCAMPAL REGION; FUNCTIONAL EXPRESSION; INTRINSIC CONNECTIONS; LEAK CHANNELS; RAT;
D O I
10.1016/j.neuron.2009.06.022
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The entorhinal cortex (EC) is regarded as the gateway to the hippocampus and thus is essential for learning and memory. Whereas the EC expresses a high density of GABA(B) receptors, the functions of these receptors in this region remain unexplored. Here, we examined the effects of GABA(B) receptor activation on neuronal excitability in the EC and spatial learning. Application of baclofen, a specific GABA(B) receptor agonist, inhibited significantly neuronal excitability in the EC. GABA(B) receptor-mediated inhibition in the EC was mediated via activating TREK-2, a type of two-pore domain K+ channels, and required the functions of inhibitory G proteins and protein kinase A pathway. Depression of neuronal excitability in the EC underlies GABA(B) receptor.-mediated inhibition of spatial learning as assessed by Morris water maze. Our study indicates that GABA(B) receptors exert a tight control over spatial learning by modulating neuronal excitability in the EC.
引用
收藏
页码:230 / 243
页数:14
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