Agarwood Induced Laxative Effects<i>via</i>Acetylcholine Receptors on Loperamide-Induced Constipation in Mice
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- KAKINO Mamoru
- Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
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- IZUTA Hiroshi
- Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
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- ITO Tetsuro
- Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
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- TSURUMA Kazuhiro
- Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
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- ARAKI Yoko
- Nagara Research Center, API Co., Ltd.
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- SHIMAZAWA Masamitsu
- Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
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- OYAMA Masayoshi
- Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
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- IINUMA Munekazu
- Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
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- HARA Hideaki
- Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
書誌事項
- タイトル別名
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- Agarwood Induced Laxative Effects via Acetylcholine Receptors on Loperamide-Induced Constipation in Mice
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抄録
Agarwood (Aquilaria sinensis, Aquilaria crasna) is well known as an incense in the oriental region such as Thailand, Taiwan, and Cambodia, and is used as a digestive in traditional medicine. We investigated the laxative effects and mechanism of agarwood leaves extracted with ethanol (EEA-1, Aquilaria sinensis; EEA-2, Aquilaria crasna). EEA-1, EEA-2, the main constituents of EEAs (mangiferin, and genkwanin-5-O-primeveroside), and senna increased the frequency and weight of stools in loperamide-induced constipation model mice. EEA-1 and EEA-2 did not induce diarrhea as a side effect, but senna induced severe diarrhea. EEA-1 and senna increased gastro-intestinal (GI) transit in the model mice. EEA-1, but not senna, also increased the intestinal tension of isolated jejunum and ileum in guinea pigs, and the tension increase was blocked by atropine, a muscarinic receptor antagonist, but not by other inhibitors (granicetron, pyrilamine, or bradykinin-antagonist peptide). Furthermore, the increase in frequency and weight of stools induced by EEA-1 were blocked by pre-administration of atropine in the model mice. These findings indicate that EEAs exerted a laxative effect via acetylcholine receptors in the mouse constipation model.
収録刊行物
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- Bioscience, Biotechnology, and Biochemistry
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Bioscience, Biotechnology, and Biochemistry 74 (8), 1550-1555, 2010
公益社団法人 日本農芸化学会
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詳細情報 詳細情報について
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- CRID
- 1390001206477285248
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- NII論文ID
- 10027557930
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- NII書誌ID
- AA10824164
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- ISSN
- 13476947
- 09168451
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- NDL書誌ID
- 10836390
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- NDL
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