Effects of cloperastine, a non-narcotic antitussive, on the expression of GIRK channels in the brain of methamphetamine-induced hyperactive mice

Q4 Pharmacology, Toxicology and Pharmaceutics
F. Soeda, Mizue Kinoshita, Yoshiko Fujieda, K. Takahama
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引用次数: 0

Abstract

Centrally-acting antitussives with inhibitory effects on G protein-coupled inwardly rectifying potassium (GIRK) channels have been shown to also inhibit methamphetamine-induced hyperactivity in mice. In this study, we examined if cloperastine, which is the most potent inhibitor of the GIRK channels among antitussives, is sensitive to the expression levels of GIRK channels in the brain of methamphetamine-treated mice. The brain tissues have been removed and the total RNA has been extracted from tissues. The mRNA levels were evaluated using semiquantitative reverse transcription-polymerase chain reaction. The concentration levels of the mRNA of GIRK channels within the ventral midbrain of methamphetamine-treated mice increased as compared with that in control and cloperastine reduced an upregulation in GIRK2, one of the subunits of the GIRK channels, by the injection of methamphetamine. These findings suggest that cloperastine might ameliorate hyperactivity by inhibiting the GIRK channels in the brain.
非麻醉性镇咳药cloperastine对甲基苯丙胺致多动小鼠脑内GIRK通道表达的影响
对G蛋白偶联内向整流钾(GIRK)通道具有抑制作用的中心作用镇咳药已被证明也能抑制甲基苯丙胺诱导的小鼠多动。在这项研究中,我们检测了作为镇咳药中最有效的GIRK通道抑制剂的氯拉司汀是否对甲基苯丙胺处理小鼠大脑中GIRK渠道的表达水平敏感。已经移除了脑组织,并且已经从组织中提取了总RNA。使用半定量逆转录聚合酶链反应评估mRNA水平。与对照组相比,甲基苯丙胺处理的小鼠腹侧中脑内GIRK通道的mRNA浓度水平增加,并且通过注射甲基苯丙胺,cloperastine减少了GIRK2(GIRK渠道的亚基之一)的上调。这些发现表明,cloperastine可能通过抑制大脑中的GIRK通道来改善多动。
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来源期刊
Indian journal of physiology and pharmacology
Indian journal of physiology and pharmacology Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
0.50
自引率
0.00%
发文量
35
期刊介绍: Indian Journal of Physiology and Pharmacology (IJPP) welcomes original manuscripts based upon research in physiological, pharmacological and allied sciences from any part of the world.
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