Ho Shih-Yin, Chien Yin-Hsiu, Tsai Li-Kai, Muramatsu Shin-Ichi, Hwu Wuh-Liang, Liou Horng-Huei, Lee Ni-Chung
Department of Neurology, National Taiwan University Hospital, Taipei, Taiwan.
Department of Pharmacology, College of Medicine, National Taiwan University, Taipei, Taiwan.
Front Cell Neurosci. 2019 Jan 31;13:9. doi: 10.3389/fncel.2019.00009. eCollection 2019.
Aromatic L-acid decarboxylase (AADC) deficiency causes severe motor disturbances in affected children. A putamen-targeted gene therapy improves the motor function of patients. The present study investigated the electrical properties of dopaminergic (DA) neurons in the substantia nigra compacta (SNc) of mice with an AADC deficiency (Ddc). The basal firing of DA neurons, which determines DA release in the putamen, was abnormal in the Ddc mice, including a low frequency and irregular firing pattern, because of a decrease in the after-hyperpolarization (AHP) amplitude of action potentials (APs). The frequency of spontaneous excitatory postsynaptic currents (sEPSCs) increased and that of spontaneous inhibitory PSCs (sIPSCs) decreased in the SNc DA neurons from the Ddc mice, suggesting an elevation in glutamatergic excitatory stimuli and a reduction in GABAergic inhibitory stimuli, respectively. Altered expression patterns of genes encoding receptors and channels were also observed in the Ddc mice. Administration of a widespread neuron-specific gene therapy to the brains of the Ddc mice partially corrected these electric abnormalities. The overexcitability of SNc DA neurons in the presence of generalized dopamine deficiency likely underlies the occurrence of motor disturbances.
芳香族L-酸脱羧酶(AADC)缺乏症会导致患病儿童出现严重的运动障碍。一种针对壳核的基因疗法可改善患者的运动功能。本研究调查了AADC缺乏(Ddc)小鼠黑质致密部(SNc)中多巴胺能(DA)神经元的电特性。由于动作电位(AP)的超极化后电位(AHP)幅度降低,决定壳核中DA释放的DA神经元的基础放电在Ddc小鼠中异常,包括低频和不规则放电模式。Ddc小鼠SNc DA神经元中自发兴奋性突触后电流(sEPSCs)的频率增加,而自发抑制性PSC(sIPSCs)的频率降低,这分别表明谷氨酸能兴奋性刺激增加和GABA能抑制性刺激减少。在Ddc小鼠中还观察到编码受体和通道的基因表达模式改变。对Ddc小鼠大脑进行广泛的神经元特异性基因疗法部分纠正了这些电异常。在普遍存在多巴胺缺乏的情况下,SNc DA神经元的过度兴奋性可能是运动障碍发生的基础。
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