Differential effects of statins on the anti-dyskinetic activity of sub-anesthetic ketamine

IF 2.5 4区 医学 Q3 NEUROSCIENCES Neuroscience Letters Pub Date : 2025-02-06 DOI:10.1016/j.neulet.2025.138114
Mitchell J. Bartlett , Carolyn J. Stopera , Stephen L. Cowen , Scott J. Sherman , Torsten Falk
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Abstract

Sub-anesthetic ketamine has been demonstrated to reduce abnormal involuntary movements (AIMs) in preclinical models of L-DOPA-induced dyskinesia (LID) and retrospective Parkinson’s disease (PD) case reports. In this study, we examined the effects on LID of two different statins alone and in combination with ketamine in unilateral 6-hydroxydopamine-lesioned male rats, the standard model for preclinical LID studies. Ketamine attenuated the development of AIMs, while the non-polar lovastatin only showed anti-dyskinetic activity early in the priming period but did not prevent the development of LID, and the polar pravastatin showed no anti-dyskinetic activity. Furthermore, our main result is that pravastatin blocked the long-term neuroplastic anti-dyskinetic effects of ketamine, while lovastatin did not. This study shows two different statins affect LID and the anti-dyskinetic activity of ketamine differentially, pointing to an important drug interaction. The results further inform and support ongoing clinical testing of sub-anesthetic ketamine to treat LID in individuals with PD.
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他汀类药物对亚麻醉氯胺酮抗运动障碍活性的不同影响。
在左旋多巴诱导的运动障碍(LID)的临床前模型和回顾性帕金森病(PD)病例报告中,亚麻醉氯胺酮已被证明可以减少异常不自主运动(AIMs)。在这项研究中,我们研究了两种不同的他汀类药物单独使用和与氯胺酮联合使用对单侧6-羟多巴胺损伤的雄性大鼠(临床前LID研究的标准模型)的LID的影响。氯胺酮可减弱AIMs的发展,而非极性洛伐他汀仅在启动期早期表现出抗运动障碍活性,但不能阻止LID的发展,极性普伐他汀无抗运动障碍活性。此外,我们的主要结果是普伐他汀阻断了氯胺酮的长期神经可塑性抗运动障碍作用,而洛伐他汀没有。本研究显示两种不同的他汀类药物对LID和氯胺酮抗运动障碍活性的影响不同,指出了一种重要的药物相互作用。该结果进一步为亚麻醉氯胺酮治疗PD患者LID的临床试验提供了信息和支持。
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来源期刊
Neuroscience Letters
Neuroscience Letters 医学-神经科学
CiteScore
5.20
自引率
0.00%
发文量
408
审稿时长
50 days
期刊介绍: Neuroscience Letters is devoted to the rapid publication of short, high-quality papers of interest to the broad community of neuroscientists. Only papers which will make a significant addition to the literature in the field will be published. Papers in all areas of neuroscience - molecular, cellular, developmental, systems, behavioral and cognitive, as well as computational - will be considered for publication. Submission of laboratory investigations that shed light on disease mechanisms is encouraged. Special Issues, edited by Guest Editors to cover new and rapidly-moving areas, will include invited mini-reviews. Occasional mini-reviews in especially timely areas will be considered for publication, without invitation, outside of Special Issues; these un-solicited mini-reviews can be submitted without invitation but must be of very high quality. Clinical studies will also be published if they provide new information about organization or actions of the nervous system, or provide new insights into the neurobiology of disease. NSL does not publish case reports.
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