TY - JOUR
T1 - GABA transporter-1 activity modulates hippocampal theta oscillation and theta burst stimulation-induced long-term potentiation
AU - Gong, Neng
AU - Li, Yong
AU - Cai, Guo Qiang
AU - Niu, Rui Fang
AU - Fang, Qi
AU - Wu, Kun
AU - Chen, Zhong
AU - Lin, Long Nian
AU - Xu, Lin
AU - Fei, Jian
AU - Xu, Tian Le
PY - 2009/12/16
Y1 - 2009/12/16
N2 - The network oscillation and synaptic plasticity are known to be regulated by GABAergic inhibition, but how they are affected by changes in the GABA transporter activity remains unclear. Here we show that in the CA1 region of mouse hippocampus, pharmacological blockade or genetic deletion of GABA transporter-1 (GAT1) specifically impaired long-term potentiation (LTP) induced by theta burst stimulation, but had no effect on LTP induced by high-frequency stimulation or long-term depression induced by low-frequency stimulation. The extent of LTP impairment depended on the precise burst frequency, with significant impairment at 3-7 Hz that correlated with the time course of elevated GABAergic inhibition caused by GAT1 disruption. Furthermore, in vivo electrophysiological recordings showed that GAT1 gene deletion reduced the frequency of hippocampal theta oscillation. Moreover, behavioral studies showed that GAT1 knock-out mice also exhibited impaired hippocampus-dependent learning and memory. Together, these results have highlighted the important link between GABAergic inhibition and hippocampal theta oscillation, both of which are critical for synaptic plasticity and learning behaviors.
AB - The network oscillation and synaptic plasticity are known to be regulated by GABAergic inhibition, but how they are affected by changes in the GABA transporter activity remains unclear. Here we show that in the CA1 region of mouse hippocampus, pharmacological blockade or genetic deletion of GABA transporter-1 (GAT1) specifically impaired long-term potentiation (LTP) induced by theta burst stimulation, but had no effect on LTP induced by high-frequency stimulation or long-term depression induced by low-frequency stimulation. The extent of LTP impairment depended on the precise burst frequency, with significant impairment at 3-7 Hz that correlated with the time course of elevated GABAergic inhibition caused by GAT1 disruption. Furthermore, in vivo electrophysiological recordings showed that GAT1 gene deletion reduced the frequency of hippocampal theta oscillation. Moreover, behavioral studies showed that GAT1 knock-out mice also exhibited impaired hippocampus-dependent learning and memory. Together, these results have highlighted the important link between GABAergic inhibition and hippocampal theta oscillation, both of which are critical for synaptic plasticity and learning behaviors.
UR - https://www.scopus.com/pages/publications/72449181682
U2 - 10.1523/JNEUROSCI.4643-09.2009
DO - 10.1523/JNEUROSCI.4643-09.2009
M3 - 文章
C2 - 20016099
AN - SCOPUS:72449181682
SN - 0270-6474
VL - 29
SP - 15836
EP - 15845
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 50
ER -