Adenosine A2A signals and dystonia.

International review of neurobiology Pub Date : 2023-01-01 Epub Date: 2023-07-27 DOI:10.1016/bs.irn.2023.06.001
Makio Takahashi
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引用次数: 0

Abstract

Dystonia is a movement disorder characterized by sustained or intermittent involuntary muscle contractions, which is also seen in an advanced stage of Parkinson's disease (PD) as camptocormia, torticollis, and Pisa syndrome. Istradefylline, an adenosine A2A receptor antagonist, can be used for the treatment of PD to reduce 'off'-time period, and several clinical studies demonstrated the improvement of camptocormia, which have many similar features to dopa-responsive/non-responsive dystonia. Many animal models of dystonia showed that adenosine A2A receptor colocalized with dopamine D2 positive spiny projection neurons in indirect pathway of basal ganglia circuit, and also in the cholinergic interneurons that affects the balance of indirect and direct pathway of basal ganglia. In this chapter, the potential effect of adenosine A2A antagonism on dystonia was discussed in view of clinical studies of PD with postural abnormalities and the findings of dystonia mouse models.

腺苷A2A信号与肌张力障碍。
肌张力障碍是一种运动障碍,其特征是持续或间歇性的不自主肌肉收缩,在帕金森病(PD)的晚期也可以看到,如camptocoria、斜颈和Pisa综合征。作为一种腺苷A2A受体拮抗剂,依斯替可可碱可用于治疗帕金森病,以缩短“关闭”时间,几项临床研究表明,camptocormia具有许多与多巴反应性/非反应性肌张力障碍相似的特征。许多肌张力障碍动物模型显示,腺苷A2A受体与多巴胺D2阳性棘突投射神经元在基底节回路的间接通路以及影响基底节间接通路和直接通路平衡的胆碱能中间神经元中共定位。在本章中,根据姿势异常PD的临床研究和肌张力障碍小鼠模型的发现,讨论了腺苷A2A拮抗剂对肌张力障碍的潜在影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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