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Adenosine A(2A) Receptor Modulates the Activity of Globus Pallidus Neurons in Rats

The globus pallidus is a central nucleus in the basal ganglia motor control circuit. Morphological studies have revealed the expression of adenosine A(2A) receptors in the globus pallidus. To determine the modulation of adenosine A(2A) receptors on the activity of pallidal neurons in both normal and...

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Detalles Bibliográficos
Autores principales: Diao, Hui-Ling, Xue, Yan, Han, Xiao-Hua, Wang, Shuang-Yan, Liu, Cui, Chen, Wen-Fang, Chen, Lei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5682020/
https://www.ncbi.nlm.nih.gov/pubmed/29163226
http://dx.doi.org/10.3389/fphys.2017.00897
Descripción
Sumario:The globus pallidus is a central nucleus in the basal ganglia motor control circuit. Morphological studies have revealed the expression of adenosine A(2A) receptors in the globus pallidus. To determine the modulation of adenosine A(2A) receptors on the activity of pallidal neurons in both normal and parkinsonian rats, in vivo electrophysiological and behavioral tests were performed in the present study. The extracellular single unit recordings showed that micro-pressure administration of adenosine A(2A) receptor agonist, CGS21680, regulated the pallidal firing activity. GABAergic neurotransmission was involved in CGS21680-induced modulation of pallidal neurons via a PKA pathway. Furthermore, application of two adenosine A(2A) receptor antagonists, KW6002 or SCH442416, mainly increased the spontaneous firing of pallidal neurons, suggesting that endogenous adenosine system modulates the activity of pallidal neurons through adenosine A(2A) receptors. Finally, elevated body swing test (EBST) showed that intrapallidal microinjection of adenosine A(2A) receptor agonist/antagonist induced ipsilateral/contralateral-biased swing, respectively. In addition, the electrophysiological and behavioral findings also revealed that activation of dopamine D(2) receptors by quinpirole strengthened KW6002/SCH442416-induced excitation of pallidal activity. Co-application of quinpirole with KW6002 or SCH442416 alleviated biased swing in hemi-parkinsonian rats. Based on the present findings, we concluded that pallidal adenosine A(2A) receptors may be potentially useful in the treatment of Parkinson's disease.