Thioxanthenes, chlorprothixene and flupentixol inhibit proton currents in BV2 microglial cells
- Authors
- Kim, Jiwon; Song, Jin-Ho
- Issue Date
- May-2016
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- Chlorprothixene; Flupentixol; Microglia; Proton channel; Thioxanthenes
- Citation
- EUROPEAN JOURNAL OF PHARMACOLOGY, v.779, pp 31 - 37
- Pages
- 7
- Journal Title
- EUROPEAN JOURNAL OF PHARMACOLOGY
- Volume
- 779
- Start Page
- 31
- End Page
- 37
- URI
- https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/6938
- DOI
- 10.1016/j.ejphar.2016.03.009
- ISSN
- 0014-2999
1879-0712
- Abstract
- The thioxanthene antipsychotic drugs chlorprothixene and flupentixol have anti-inflammatory and anti-oxidant properties. The reactive oxygen species produced by NADPH oxidase during microglia-mediated inflammatory responses cause neuronal damage, thereby contributing to various neurodegenerative diseases. Voltage-gated proton channels sustain the NADPH oxidase activity, and inhibition of the channels' activity reduces the production of reactive oxygen species. Herein, the effects of chlorprothixene and flupentixol on proton currents were investigated in BV2 microglial cells using the whole cell patch-clamp method. Both drugs inhibited the proton currents in a concentration-dependent manner (IC50=1.7 mu M and 6.6 LIM, respectively). Chlorprothixene at 3 mu M slightly shifted the activation voltage toward depolarization. Both the activation and the deactivation kinetics of the proton currents were slowed by chlorprothixene 12- and 3.5-fold, respectively. Thus, the inhibition of proton currents may be partly responsible for the antioxidant effects of thioxanthene antipsychotic drugs. (C) 2016 Elsevier B.V. All rights reserved.
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