Abstract

Background: Parkinson’s disease (PD) is commonly accompanied with anxiety disorder, however, the mechanisms underlying PD-mediated anxiety remain elusive. The lateral habenula (LHb) is a critical brain region that influences the activity of the monoaminergic system in the midbrain and consequently modulates anxiety. Most neurons in the LHb express AMPA receptors (AMPARs). The PD model for the pharmacological intervention of AMPA receptors was established by the unilateral lesion of the substantia nigra pars compacta (SNc) with 6-hydroxydopamine (6-OHDA). Methods: The AMPAR agonist (S)-AMPA and antagonist NBQX were microinjected into the LHb, respectively, to examine whether anxiety-like behaviors were altered in sham-operated and SNc-lesion rats, measured with the paradigms of the open-field test (OPT) and elevated plus maze (EPM). Furthermore, dopamine (DA) and 5-hydroxytryptamine (5-HT) levels in the basolateral amygdala (BLA) were measured using in vivo microdialysis immediately following the injections of (S)-AMPA and NBQX into the LHb. Results: Activation of LHb AMPA receptors by (S)-AMPA produced anxiolytic-like behaviors and enhanced the extracellular DA and 5-HT in the BLA. Conversely, NBQX induced anxiety-like effects and suppressed the extracellular DA and 5-HT in the BLA. In addition, the minimal doses inducing the effects in the SNc-lesion rats were lower than those in sham-operated rats. Conclusion: These findings suggest that the effects of AMPA receptors in the LHb on anxiety-like behaviors likely involve the extracellular levels of DA and 5-HT in the BLA. The present results may improve our understanding of the neuropathology and/or treatment of PD.

Highlights

  • The lateral habenula (LHb) is a crucial structure of the epithalamus, and neuronal axons from the LHb project onto monoaminergic neurons in the midbrain (Bernard and Veh, 2012)

  • In contrast to the effects of (S)-AMPA, post hoc analyses indicated that treatment with NBQX robustly reduced the time spent in central area in the two groups. These results indicate that (S)-AMPA injections suppressed anxiety-like behaviors, while NBQX treatment augmented anxiety-like behaviors, and the dose required to produce a change in the anxiety-like phenotype in the substantia nigra pars compacta (SNc)-lesion rats was lower than that in sham-operated ones (for (S)-AMPA: sham-operated vs. SNc-lesion: 0.075 μg vs. 0.0375 μg, Figure 4A; for NBQX: sham-operated vs. SNc-lesion: 1.0 μg vs. 0.05 μg, Figure 4B)

  • Our study shows that activation of LHb AMPA receptors (AMPARs) produced an anxiolytic-like effect in both shamoperated rats and SNc-lesion rats. (S)-AMPA injected into the LHb significantly raised anxiety-like behaviors in the open field test (OFT) and elevated plus maze (EPM) tests, while blockade of LHb AMPARs using NBQX produced an anxiety-like behavior in both groups and suppressed the anxiety-like phenotypes in rats

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Summary

Introduction

The lateral habenula (LHb) is a crucial structure of the epithalamus, and neuronal axons from the LHb project onto monoaminergic neurons in the midbrain (Bernard and Veh, 2012). Increasing studies suggest that the LHb is highly involved in the regulation of anxiety-like behaviors; for example, the rats refraining from chronic excessive alcohol consumption showed an anxiety-like phenotype, an increase in glutamate release, and hyperactivity of LHb neurons (Kurumaji et al, 2003; Berger et al, 2018). Blocking glutamate transmission or LHb neuronal activity rescued anxiety-like behaviors in alcohol-depriving rats and suppressed alcohol intake upon the reexposure to alcohol (Li et al, 2017; Shah et al, 2017; Kang et al, 2018; Fu et al, 2020). The lateral habenula (LHb) is a critical brain region that influences the activity of the monoaminergic system in the midbrain and modulates anxiety. The PD model for the pharmacological intervention of AMPA receptors was established by the unilateral lesion of the substantia nigra pars compacta (SNc) with 6-hydroxydopamine (6-OHDA)

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