4.7 Article

Zonisamide regulates basal ganglia transmission via astroglial kynurenine pathway

Journal

NEUROPHARMACOLOGY
Volume 76, Issue -, Pages 137-145

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuropharm.2013.08.002

Keywords

Zonisamide; Astrocyte; Kynurenine pathway; Xanthurenic acid; Cinnabarinic acid; Parkinson's disease

Funding

  1. Japanese Ministry of Education, Science and Culture [23659564, 22390224]
  2. Japan Epilepsy Research Foundation
  3. Grants-in-Aid for Scientific Research [23659564, 22390224] Funding Source: KAKEN

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To clarify the anti-parkinsonian mechanisms of action of zonisamide (ZNS), we determined the effects of ZNS on tripartite synaptic transmission associated with kynurenine (KYN) pathway (KP) in cultured astrocytes, and transmission in both direct and indirect pathways of basal ganglia using microdialysis. Interactions between cytokines [interferon-gamma (IFN gamma) and tumor-necrosis factor-alpha (TNF alpha)] and ZNS on astroglial releates of KP metabolites, KYN, kynurenic-acid (KYNA), xanthurenic-acid (XTRA), cinnabarinicacid (CNBA) and quinolinic-acid (QUNA), were determined by extreme liquid-chromatography with massspectrometry. Interaction among metabotropic glutamate-receptor (mGluR), KP metabolites and ZNS on striato-nigral, striato-pallidal GABAergic and subthalamo-nigral glutamatergic transmission was examined by microdialysis with extreme liquid-chromatography fluorescence resonance-energy transfer detection. Acute and chronic ZNS administration increased astroglial release of KYN, KYNA, XTRA and CNBA, but not QUNA. Chronic IFN gamma administration increased the release of KYN, KYNA, CNBA and QUNA, but had minimal inhibitory effect on XTRA release. Chronic TNFa administration increased CNBA and QUNA, but not KYN, KYNA or XTRA. ZNS inhibited IFN gamma-induced elevation of KYN, MYNA and QUNA, but enhanced IFN gamma-induced that of CNBA. TNF alpha-induced rises in CNBA and QUNA were inhibited by ZNS. ZNS inhibited striato-nigral GABAergic, striato-pallidal GABAergic and subthalamo-nigral glutamatergic transmission via activation of groups II and III mGluRs. ZNS enhanced astroglial release of endogenous agonists of group II mGluR, XTRA and group III mGluR, CNBA. Activated endogenous mGluR agonists inhibited transmission in direct and indirect pathways of basal ganglia. These mechanisms contribute to effectiveness and well tolerability of ZNS as an adjunct treatment for Parkinson's disease during L-DOPA monotherapy. (C) 2013 Elsevier Ltd. All rights reserved.

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