TY - JOUR
T1 - Differential effects of statins on the anti-dyskinetic activity of sub-anesthetic ketamine
AU - Bartlett, Mitchell J.
AU - Stopera, Carolyn J.
AU - Cowen, Stephen L.
AU - Sherman, Scott J.
AU - Falk, Torsten
N1 - Publisher Copyright:
© 2025
PY - 2025/2/6
Y1 - 2025/2/6
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85214348164&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85214348164&partnerID=8YFLogxK
U2 - 10.1016/j.neulet.2025.138114
DO - 10.1016/j.neulet.2025.138114
M3 - Article
AN - SCOPUS:85214348164
SN - 0304-3940
VL - 848
JO - Neuroscience Letters
JF - Neuroscience Letters
M1 - 138114
ER -