Synaptic and membrane properties of cholinergic interneurons in the striatum of aristaless-related homeobox gene mutant mice

被引:0
|
作者
Momiyama, Toshihiko [1 ]
Nishijo, Takuma [1 ,2 ]
Suzuki, Etsuko [1 ]
Kitamura, Kunio [3 ]
机构
[1] Jikei Univ, Dept Pharmacol, Sch Med, Minato Ku, Tokyo 1058461, Japan
[2] Aichi Dev Disabil Ctr, Inst Dev Res, Dept Mol Neurobiol, Kasugai, Aichi, Japan
[3] Natl Inst Neurosci, Natl Ctr Neurol & Psychiat, Dept Mental Retardat & Birth Defect Res, Kodaira, Tokyo, Japan
关键词
aristaless-related homeobox gene; patch-clamp; slices; striatum; synaptic transmission; PAIRED-PULSE FACILITATION; LONG-TERM POTENTIATION; NEURONAL MIGRATION; INFANTILE SPASMS; ARX; TELENCEPHALON; PHENOTYPES; RELEASE; IDENTIFICATION; TRANSMISSION;
D O I
10.1111/ejn.16542
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A whole-cell patch-clamp study was carried out to investigate membrane and synaptic properties of cholinergic interneurons in the striatum of aristaless-related homeobox gene (ARX) mutant mice. Brain slices were prepared from mice knocked in two types of ARX, P355L (PL) and 333ins (GCG)7 (GCG). The input resistance of cholinergic interneurons in PL or GCG mice was significantly smaller than that in wild type (WT), whereas resting membrane potential, threshold of action potentials, spontaneous firing rate, sag ratio or afterhyperpolarization of the mutant mice were not significantly different from those of WT mice. In GCG mice, NMDA/AMPA ratio of excitatory postsynaptic currents (EPSCs) evoked in cholinergic interneurons was significantly smaller than that in WT and PL mice, whereas the ratio between PL and WT mice was not significantly different. Although inhibitory effects induced by dopamine D2-like receptor activation on the inhibitory postsynaptic currents (IPSCs) were not significantly different between WT and PL or GCG mice, increase in the paired pulse ratio of IPSCs by dopamine D2-like receptor activation was abolished in PL and GCG mice. The present results have found abnormalities of neuronal activities as well as its modulation in the basal ganglia in ARX mutant mice, clarifying basic mechanisms underlying related disorders.
引用
收藏
页码:6015 / 6029
页数:15
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