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首页> 外文期刊>Frontiers in Molecular Neuroscience >MPTP-Induced Dopamine Depletion in Basolateral Amygdala via Decrease of D2R Activation Suppresses GABA A Receptors Expression and LTD Induction Leading to Anxiety-Like Behaviors
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MPTP-Induced Dopamine Depletion in Basolateral Amygdala via Decrease of D2R Activation Suppresses GABA A Receptors Expression and LTD Induction Leading to Anxiety-Like Behaviors

机译:MPTP诱导的基底外侧杏仁核中多巴胺的消耗,通过D2R激活的降低来抑制GABA A 受体的表达和LTD诱导导致焦虑行为

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Anxiety disorders commonly occur in Parkinson’s disease. Using field potential recording and patch-clamp recording, we evaluated influence of MPTP-reduced dopaminergic afferent in basolateral amygdala (BLA), a main region for affective regulation, on excitatory–inhibitory circuits and synaptic plasticity. Field excitatory post-synaptic potential (fEPSP) slopes at external capsule-BLA synapses were increased in MPTP-mice with decreases in paired-pulse facilitation and long-term potentiation amplitude, which were corrected by bath-application of D2R agonist quinpirole or cannabinoid type 1 receptors agonist WIN55,212-2, but not D1R agonist SKF38393. Compared to single waveform fEPSP in control mice, a multi-spike waveform fEPSP was observed in MPTP-mice with prolongation of duration and an increase in paired-pulse inhibition, which were recovered by BLA-injection of quinpirole for 2 days rather than bath-application. Density of GABA-evoked current ( I _(GABA)) in BLA principal neurons and GABA_(A)R-α2 subunit expression were reduced in MPTP-mice, which were recovered by administration of quinpirole. Decline of PKC phosphorylation in BLA of MPTP-mice was corrected by bath-application of quinpirole, but not SKF38393. In MPTP-mice, BLA-injection of quinpirole or PKC activator PMA could recover GABA_(A)R expression, which was sensitive to PKC inhibitor GF109203X. The impairment of long-term depression (LTD) in MPTP-mice was rescued by bath-application of GABA_(A)R agonist muscimol or BLA-injection of quinpirole and PMA. Finally, BLA-injection of muscimol, quinpirole or PMA relieved anxiety-like behaviors in MPTP-mice. The results indicate that the MPTP-induced dopamine depletion in BLA principal neurons through reducing D2R-mediated PKC phosphorylation suppresses GABA_(A)R expression and activity, which impairs GABA_(A)R-mediated inhibition and LTD induction leading to anxiety-like behaviors.
机译:帕金森氏病通常会引起焦虑症。使用场电位记录和膜片钳记录,我们评估了兴奋性抑制电路和突触可塑性对基底外侧杏仁核(BLA)(情感调节的主要区域)中MPTP降低的多巴胺能传入的影响。 MPTP小鼠外膜-BLA突触的场兴奋性突触后电位(fEPSP)斜率增加,成对脉冲促进作用和长期增强幅度降低,这可通过D2R激动剂喹吡罗或大麻素型浴应用来纠正1个受体激动剂WIN55,212-2,但不是D1R激动剂SKF38393。与对照小鼠中的单波形fEPSP相比,在MPTP小鼠中观察到多峰波形fEPSP,且持续时间延长且配对脉冲抑制增加,这可通过BLA注射喹吡罗2天而不是用浴法恢复。应用。 MPTP小鼠的BLA主要神经元中GABA诱发的电流(I _(GABA))的密度和GABA_(A)R-α2亚基表达降低,这些剂量可通过服用喹吡罗恢复。 MPTP小鼠的BLA中PKC磷酸化水平的下降可通过应用喹吡罗(而非SKF38393)来纠正。在MPTP小鼠中,BLA注射喹吡罗或PKC激活剂PMA可以恢复对PKC抑制剂GF109203X敏感的GABA_(A)R表达。通过沐浴应用GABA_(A)R激动剂麝香酚或BLA注射喹吡罗和PMA可以挽救MPTP小鼠的长期抑郁症(LTD)。最后,BLA注射麝香酚,喹吡罗或PMA可缓解MPTP小鼠的焦虑样行为。结果表明,MPTP通过减少D2R介导的PKC磷酸化引起的BLA主神经元中的多巴胺耗竭,抑制了GABA_(A)R的表达和活性,从而削弱了GABA_(A)R介导的抑制和LTD的诱导,导致了焦虑样行为。 。

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