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Atp1a3基因杂合缺失的小鼠在慢性束缚应激下表现出运动功能障碍。

Heterozygous mice deficient in Atp1a3 exhibit motor deficits by chronic restraint stress.

作者信息

Sugimoto Hiroki, Ikeda Keiko, Kawakami Kiyoshi

机构信息

Division of Biology, Center for Molecular Medicine, Jichi Medical University, Shimotsuke 329-0498, Tochigi, Japan.

Division of Biology, Center for Molecular Medicine, Jichi Medical University, Shimotsuke 329-0498, Tochigi, Japan; Biology, Hyogo Medical College, Nishinomiya 663-8501, Hyogo, Japan.

出版信息

Behav Brain Res. 2014 Oct 1;272:100-10. doi: 10.1016/j.bbr.2014.06.048. Epub 2014 Jun 29.

Abstract

Dystonia is a neurological disorder with involuntary and simultaneous contractions of agonist and antagonist muscles. Rapid-onset dystonia parkinsonism (RDP), one of the heredity forms of dystonia, is caused by mutations of Na,K-ATPase α3 subunit gene (ATP1A3). The abrupt onset of bulbar and limb symptoms of RDP are often triggered by physical and/or emotional stress. We reported previously that Atp1a3-deficient heterozygous mice showed higher locomotor activity and developed enhanced dystonia symptoms after kainate injection into the cerebellum, but not spontaneous movement disorder like RDP patients. Here we show that Atp1a3-deficient heterozygous mice exhibited shorter stride length at 4 weeks of age without stress and at later stages under chronic restraint stress loading. Shorter hanging time in the hanging box test was also observed after stress loading. Shorter stride length and hanging time may be relevant to certain phenotypes, such as gait abnormality, observed in RDP patients. Atp1a3 was widely expressed in the brain, including basal ganglia and cerebellum, and spinal cord of young mice, and the expression pattern was compatible with movement abnormalities under lack of one of alleles. Our results demonstrated the usefulness of Atp1a3-deficient heterozygous mice as an animal model of RDP and its potential use to explore the pathophysiology of movement abnormality in this disorder.

摘要

肌张力障碍是一种神经疾病,其特征为主动肌和拮抗肌同时发生不自主收缩。快速起病的肌张力障碍帕金森综合征(RDP)是肌张力障碍的一种遗传形式,由钠钾ATP酶α3亚基基因(ATP1A3)突变引起。RDP的延髓和肢体症状突然发作,常由身体和/或情绪应激触发。我们之前报道过,Atp1a3基因缺陷的杂合小鼠在向小脑注射红藻氨酸后表现出更高的运动活性,并出现加重的肌张力障碍症状,但不像RDP患者那样出现自发运动障碍。在此我们表明,Atp1a3基因缺陷的杂合小鼠在4周龄时无应激状态下以及在慢性束缚应激负荷下的后期阶段,步幅长度较短。在应激负荷后,还观察到在悬垂箱试验中的悬垂时间较短。较短的步幅长度和悬垂时间可能与RDP患者中观察到的某些表型有关,如步态异常。Atp1a3在幼鼠的大脑(包括基底神经节和小脑)以及脊髓中广泛表达,其表达模式与等位基因之一缺失时的运动异常情况相符。我们的结果证明了Atp1a3基因缺陷的杂合小鼠作为RDP动物模型的有用性及其在探索该疾病运动异常病理生理学方面的潜在用途。

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