Synaptic and membrane properties of cholinergic interneurons in the striatum of aristaless‐related homeobox gene mutant mice
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...
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Veröffentlicht in: | The European journal of neuroscience 2024-10, Vol.60 (8), p.6015-6029 |
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Zusammenfassung: | 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.
Neuronal membranes of two types of ARX mutant mice (PL and GCG) are more leaky than those of wild type (WT) mice. The NMDA/AMPA ratio of IPSCs in GCG mutant mice is smaller than that in WT or PL mutant mice. The increase in paired‐pulse ratio by D2‐like receptor activation is absent in these mutant mice. |
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ISSN: | 0953-816X 1460-9568 1460-9568 |
DOI: | 10.1111/ejn.16542 |