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論文
タイトル
タイトル(英)
Therapeutic Effects of Quetiapine and 5-HT1A Receptor Agonism on Hyperactivity in Dopamine-Deficient Mice
参照URL
https://researchmap.jp/kazutakaikeda/published_papers/40635479
著者
著者(英)
Yukiko Ochiai,Masayo Fujita,Yoko Hagino,Kazuto Kobayashi,Ryoichi Okiyama,Kazushi Takahashi,Kazutaka Ikeda
担当区分
概要
概要(英)
Some diseases that are associated with dopamine deficiency are accompanied by psychiatric symptoms, including Parkinson’s disease. However, the mechanism by which this occurs has not been clarified. Previous studies found that dopamine-deficient (DD) mice exhibited hyperactivity in a novel environment. This hyperactivity is improved by clozapine and donepezil, which are used to treat psychiatric symptoms associated with dopamine deficiency (PSDD). We considered that DD mice could be used to study PSDD. In the present study, we sought to identify the pharmacological mechanism of PSDD. We conducted locomotor activity tests by administering quetiapine and drugs that have specific actions on serotonin (5-hydroxytryptamine [5-HT]) receptors and muscarinic receptors. Changes in neuronal activity that were induced by drug administration in DD mice were evaluated by examining Fos immunoreactivity. Quetiapine suppressed hyperactivity in DD mice while the 5-HT1A receptor antagonist WAY100635 inhibited this effect. The number of Fos-positive neurons in the median raphe nucleus increased in DD mice that exhibited hyperactivity and was decreased by treatment with quetiapine and 5-HT1A receptor agonists. In conclusion, hyperactivity in DD mice was ameliorated by quetiapine, likely through 5-HT1A receptor activation. These findings suggest that 5-HT1A receptors may play a role in PSDD, and 5-HT1A receptor-targeting drugs may help improve PSDD.
出版者・発行元
出版者・発行元(英)
MDPI AG
誌名
誌名(英)
International Journal of Molecular Sciences
23
13
開始ページ
7436
終了ページ
7436
出版年月
2022年7月4日
査読の有無
招待の有無
掲載種別
研究論文(学術雑誌)
ISSN
DOI URL
https://doi.org/10.3390/ijms23137436
共同研究・競争的資金等の研究課題
研究者
池田 和隆 (イケダ カズタカ) , 藤田 雅代 ( )