Ophthalmate is a new regulator of motor functions via CaSR: implications for movement disorders.

IF 10.6 1区 医学 Q1 CLINICAL NEUROLOGY Brain Pub Date : 2024-10-03 DOI:10.1093/brain/awae097
Sammy Alhassen, Derk Hogenkamp, Hung Anh Nguyen, Saeed Al Masri, Geoffrey W Abbott, Olivier Civelli, Amal Alachkar
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Abstract

Dopamine's role as the principal neurotransmitter in motor functions has long been accepted. We broaden this conventional perspective by demonstrating the involvement of non-dopaminergic mechanisms. In mouse models of Parkinson's disease, we observed that L-DOPA elicited a substantial motor response even when its conversion to dopamine was blocked by inhibiting the enzyme aromatic amino acid decarboxylase (AADC). Remarkably, the motor activity response to L-DOPA in the presence of an AADC inhibitor (NSD1015) showed a delayed onset, yet greater intensity and longer duration, peaking at 7 h, compared to when L-DOPA was administered alone. This suggests an alternative pathway or mechanism, independent of dopamine signalling, mediating the motor functions. We sought to determine the metabolites associated with the pronounced hyperactivity observed, using comprehensive metabolomics analysis. Our results revealed that the peak in motor activity induced by NSD1015/L-DOPA in Parkinson's disease mice is associated with a surge (20-fold) in brain levels of the tripeptide ophthalmic acid (also known as ophthalmate in its anionic form). Interestingly, we found that administering ophthalmate directly to the brain rescued motor deficits in Parkinson's disease mice in a dose-dependent manner. We investigated the molecular mechanisms underlying ophthalmate's action and discovered, through radioligand binding and cAMP-luminescence assays, that ophthalmate binds to and activates the calcium-sensing receptor (CaSR). Additionally, our findings demonstrated that a CaSR antagonist inhibits the motor-enhancing effects of ophthalmate, further solidifying the evidence that ophthalmate modulates motor functions through the activation of the CaSR. The discovery of ophthalmate as a novel regulator of motor function presents significant potential to transform our understanding of brain mechanisms of movement control and the therapeutic management of related disorders.

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Ophthalmate是通过CaSR调节运动功能的新调节器:对运动障碍的影响。
多巴胺作为主要神经递质在运动功能中的作用早已为人们所接受。我们通过证明非多巴胺能机制的参与,拓宽了这一传统观点。在帕金森病(PD)小鼠模型中,我们观察到,即使通过抑制芳香族氨基酸脱羧酶(AADC)阻断了左旋多巴向多巴胺的转化,左旋多巴仍能引起大量的运动反应。值得注意的是,与单独服用 L-DOPA 相比,在 AADC 抑制剂(NSD1015)存在的情况下,L-DOPA 引起的运动反应起始时间推迟,但强度更大,持续时间更长,在 7 小时后达到峰值。这表明有一种独立于多巴胺信号传导的替代途径或机制在介导运动功能。我们试图通过全面的代谢组学分析,确定与观察到的明显过度活跃相关的代谢物。我们的研究结果表明,NSD1015/L-DOPA诱导的帕金森病小鼠运动活动的峰值与脑内三肽酞酸(OA,也称阴离子形式的酞酸)水平的激增(20倍)有关。有趣的是,我们发现将邻苯二甲酸盐直接注入大脑可以以剂量依赖的方式缓解帕金森病小鼠的运动障碍。我们研究了眼药水作用的分子机制,并通过放射性配体结合和 cAMP 发光试验发现,眼药水能与钙传感受体(CaSR)结合并激活该受体。此外,我们的研究结果表明,CaSR 拮抗剂可抑制邻苯二甲酸盐的运动增强效应,从而进一步巩固了邻苯二甲酸盐通过激活 CaSR 来调节运动功能的证据。眼药水是一种新型的运动功能调节剂,它的发现为改变我们对大脑运动控制机制的认识以及相关疾病的治疗提供了巨大的潜力。
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来源期刊
Brain
Brain 医学-临床神经学
CiteScore
20.30
自引率
4.10%
发文量
458
审稿时长
3-6 weeks
期刊介绍: Brain, a journal focused on clinical neurology and translational neuroscience, has been publishing landmark papers since 1878. The journal aims to expand its scope by including studies that shed light on disease mechanisms and conducting innovative clinical trials for brain disorders. With a wide range of topics covered, the Editorial Board represents the international readership and diverse coverage of the journal. Accepted articles are promptly posted online, typically within a few weeks of acceptance. As of 2022, Brain holds an impressive impact factor of 14.5, according to the Journal Citation Reports.
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