Postural effects of unilateral blockade of glutamatergic neurotransmission in the subthalamic nucleus on haloperidol-induced akinesia in rats

• Published in: Neuroscience letters 1998-08, Vol.252 (3), p.167-170
• Main Authors: Miwa, Hideto, Nishi, Katsunori, Fuwa, Tatsu, Mizuno, Yoshikuni
• Format: Article
• Language: English
• Subjects: 6-Cyano-7-nitroquinoxaline-2,3-dione; 6-Cyano-7-nitroquinoxaline-2,3-dione - pharmacology; Analysis of Variance; Animals; Anti-Dyskinesia Agents - toxicity; Biological and medical sciences; Central nervous system; Central neurotransmission. Neuromudulation. Pathways and receptors; Circling; Dizocilpine Maleate - pharmacology; Excitatory Amino Acid Antagonists - pharmacology; Functional Laterality - physiology; Fundamental and applied biological sciences. Psychology; Haloperidol; Haloperidol - toxicity; Male; MK-801; Movement Disorders - etiology; Parkinson's disease; Posture - physiology; Rats; Rats, Wistar; Receptors, N-Methyl-D-Aspartate - antagonists & inhibitors; Subthalamic nucleus; Synaptic Transmission - drug effects; Thalamic Nuclei - drug effects; Vertebrates: nervous system and sense organs
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/S0304-3940(98)00559-X

The present study examined the postural effects of the local application of glutamatergic antagonists unilaterally into the subthalamic nucleus (STN), on haloperidol-induced akinesia in rats. After intracerebral injections of MK-801, a selective antagonist of N-methyl- d-aspartate (NMDA) receptor, 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) disodium, a selective α-amino-3-hydroxy-5-methyl-4-isoxazole propionate (AMPA) receptor antagonist, or vehicle, unilaterally into the STN, haloperidol was administered systemically and the elicited behaviors were assessed quantitatively. In rats which received injections of MK-801 or CNQX, but not vehicle, unilaterally into the STN, the administration of haloperidol induced contraversive dystonic posturing. The severity of the deviated posturing was dose-dependent. The present findings revealed that the overactivity of the STN under conditions of dopamine blockade is suppressed by interruptions of glutamatergic inputs, mediated via both NMDA or AMPA receptors, to the STN. Therefore, the present study may provide functional evidence in support of a recently proposed hypothesis, that not only disinhibition from the inhibitory globus pallidus efferents but also excitatory glutamatergic inputs to the STN actually contribute to the overactivity of the STN under dopamine-depleted conditions.