Simultaneous Measurement of Striatal Dopamine and Hydrogen Peroxide Transients Associated with L-DOPA Induced Rotation in Hemiparkinsonian Rats

Parkinson's disease (PD) is a neurodegenerative disorder commonly treated with levodopa (L-DOPA), which eventually induces abnormal involuntary movements (AIMs). The neurochemical contributors to these dyskinesias are unknown; however, several lines of evidence indicate an interplay of dopamine...

Full description

Saved in:
Bibliographic Details
Published inACS measurement science au Vol. 2; no. 2; pp. 120 - 131
Main Authors Wilson, Leslie R, Lee, Christie A, Mason, Catherine F, Khodjaniyazova, Sitora, Flores, Kevin B, Muddiman, David C, Sombers, Leslie A
Format Journal Article
LanguageEnglish
Published United States 20.04.2022
Online AccessGet full text

Cover

Loading…
More Information
Summary:Parkinson's disease (PD) is a neurodegenerative disorder commonly treated with levodopa (L-DOPA), which eventually induces abnormal involuntary movements (AIMs). The neurochemical contributors to these dyskinesias are unknown; however, several lines of evidence indicate an interplay of dopamine (DA) and oxidative stress. Here, DA and hydrogen peroxide (H O ) were simultaneously monitored at discrete recording sites in the dorsal striata of hemiparkinsonian rats using fast-scan cyclic voltammetry. Mass spectrometry imaging validated the lesions. Hemiparkinsonian rats exhibited classic L-DOPA-induced AIMs and rotations as well as increased DA and H O tone over saline controls after 1 week of treatment. By week 3, DA tone remained elevated beyond that of controls, but H O tone was largely normalized. At this time point, rapid chemical transients were time-locked with spontaneous bouts of rotation. Striatal H O rapidly increased with the initiation of contraversive rotational behaviors in lesioned L-DOPA animals, in both hemispheres. DA signals simultaneously decreased with rotation onset. The results support a role for these striatal neuromodulators in the adaptive changes that occur with L-DOPA treatment in PD and reveal a precise interplay between DA and H O in the initiation of involuntary locomotion.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2694-250X
2694-250X
DOI:10.1021/acsmeasuresciau.1c00030