Systemic blockade of dopamine D2-like receptors increases high-voltage spindles in the globus pallidus and motor cortex of freely moving rats.
Systemic blockade of dopamine D2-like receptors increases high-voltage spindles in the globus pallidus and motor cortex of freely moving rats.
复制标题
系统性阻断多巴胺 D2 样受体会增加自由活动大鼠苍白球和运动皮层的高压纺锤体
DOI:
10.1371/journal.pone.0064637
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Gao GD
中科院分区:
文献类型:
--
作者:
Yang C;Ge SN;Zhang JR;Chen L;Yan ZQ;Heng LJ;Zhao TZ;Li WX;Jia D;Zhu JL;Gao GD
High-voltage spindles (HVSs) have been reported to appear spontaneously and widely in the cortical–basal ganglia networks of rats. Our previous study showed that dopamine depletion can significantly increase the power and coherence of HVSs in the globus pallidus (GP) and motor cortex of freely moving rats. However, it is unclear whether dopamine regulates HVS activity by acting on dopamine D1-like receptors or D2-like receptors. We employed local-field potential and electrocorticogram methods to simultaneously record the oscillatory activities in the GP and primary motor cortex (M1) in freely moving rats following systemic administration of dopamine receptor antagonists or saline. The results showed that the dopamine D2-like receptor antagonists, raclopride and haloperidol, significantly increased the number and duration of HVSs, and the relative power associated with HVS activity in the GP and M1 cortex. Coherence values for HVS activity between the GP and M1 cortex area were also significantly increased by dopamine D2-like receptor antagonists. On the contrary, the selective dopamine D1-like receptor antagonist, SCH23390, had no significant effect on the number, duration, or relative power of HVSs, or HVS-related coherence between M1 and GP. In conclusion, dopamine D2-like receptors, but not D1-like receptors, were involved in HVS regulation. This supports the important role of dopamine D2-like receptors in the regulation of HVSs. An siRNA knock-down experiment on the striatum confirmed our conclusion.
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影响因子:
82.9
作者:
Hommel, JD;Sears, RM;DiLeone, RJ
通讯作者:
DiLeone, RJ
影响因子:
2.5
作者:
Dejean, Cyril;Gross, Christian E.;Boraud, Thomas
通讯作者:
Boraud, Thomas
影响因子:
3.4
作者:
BUZSAKI, G;KENNEDY, B;ZIEGLER, M
通讯作者:
ZIEGLER, M
影响因子:
3.3
作者:
BUZSAKI, G;LASZLOVSZKY, I;VADASZ, C
通讯作者:
VADASZ, C
影响因子:
2.5
作者:
Fontanini, A;Katz, DB
通讯作者:
Katz, DB