Antagonism of kappa opioid receptors accelerates the development of L-DOPA-induced dyskinesia in a preclinical model of moderate dopamine depletion

Author:

Flores Andrew J.,Bartlett Mitchell J.,Samtani Grace,Seaton Blake T.,Sexauer Morgan R.,Weintraub Nathan C.,Siegenthaler James R.,Lu Dong,Heien Michael L.,Porreca Frank,Sherman Scott J.,Falk TorstenORCID

Abstract

AbstractLevels of the opioid peptide dynorphin, an endogenous ligand selective for kappa-opioid receptors (KORs), its mRNA and pro-peptide precursors are differentially dysregulated in Parkinson’s disease (PD) and following the development of L-DOPA-induced dyskinesia (LID). It remains unclear whether these alterations contribute to the pathophysiological mechanisms underlying PD motor impairment and the subsequent development of LID, or whether they are part of compensatory mechanisms. We sought to investigate nor-BNI, a KOR antagonist, 1) in the dopamine (DA)-depleted PD state, 2) during the development phase of LID, and 3) via measuring of tonic levels of striatal DA. While nor-BNI (3 mg/kg;s.c.) did not lead to functional restoration in the DA-depleted state, it affected the dose-dependent development of abnormal voluntary movements (AIMs) in response to escalating doses of L-DOPA in a rat PD model with a moderate striatal 6-hydroxdopamine (6-OHDA) lesion. We tested five escalating doses of L-DOPA (6, 12, 24, 48, 72 mg/kg;i.p.), and nor-BNI significantly increased the development of AIMs at the 12 and 24 mg/kg L-DOPA doses. However, after reaching the 72 mg/kg L-DOPA, AIMs were not significantly different between control and nor-BNI groups. In summary, while blocking KORs significantly increased the rate of development of LID induced by chronic, escalating doses of L-DOPA in a moderate-lesioned rat PD model, it did not contribute further once the overall severity of LID was established. While we observed an increase of tonic DA levels in the moderately lesioned dorsolateral striatum, there was no tonic DA change following administration of nor-BNI.HighlightsMild L-DOPA-induced dyskinesia develops in moderately lesioned parkinsonian ratsIn the moderately-lesioned dorsolateral striatum tonic dopamine is increasedAntagonizing dynorphin does not affect parkinsonian motor symptoms in rodentsAntagonizing dynorphin increases rate of development of L-DOPA-induced dyskinesiaTonic dopamine in dorsolateral striatum is unchanged after antagonizing dynorphin

Publisher

Cold Spring Harbor Laboratory

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