Bartlett Mitchell J, Stopera Carolyn J, Cowen Stephen L, Sherman Scott J, Falk Torsten
bioRxiv. 2024 Nov 27:2024.11.26.625570. doi: 10.1101/2024.11.26.625570.
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 case reports. In this study, we examined the effects on L-DOPA-induced dyskinesia of two statins alone and in combination with ketamine in unilateral 6-hydroxydopamine-lesioned male rats, the standard preclinical LID model. Sub-anesthetic ketamine attenuated the development of AIMs, while lovastatin only showed anti-dyskinetic activity at the beginning of the priming but did not prevent the development of LID. The polar pravastatin blocked the long-term anti-dyskinetic effects of ketamine, while the non-polar lovastatin did not. This study shows different classes of statins affect LID differentially, points to an important drug interaction and further supports ongoing clinical testing of sub-anesthetic ketamine to treat LID in individuals with Parkinson's disease.
在左旋多巴诱发异动症(LID)的临床前模型和帕金森病回顾性病例报告中,已证实亚麻醉剂量的氯胺酮可减少异常不自主运动(AIMs)。在本研究中,我们在单侧6-羟基多巴胺损伤的雄性大鼠(标准的临床前LID模型)中,研究了两种他汀类药物单独使用以及与氯胺酮联合使用对左旋多巴诱发异动症的影响。亚麻醉剂量的氯胺酮可减轻AIMs的发展,而洛伐他汀仅在启动初期显示出抗异动症活性,但不能预防LID的发展。极性的普伐他汀阻断了氯胺酮的长期抗异动症作用,而非极性的洛伐他汀则没有。本研究表明不同类别的他汀类药物对LID的影响不同,指出了一种重要的药物相互作用,并进一步支持正在进行的亚麻醉剂量氯胺酮治疗帕金森病患者LID的临床试验。