Agarwood Induced Laxative Effects<i>via</i>Acetylcholine Receptors on Loperamide-Induced Constipation in Mice

  • KAKINO Mamoru
    Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
  • IZUTA Hiroshi
    Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
  • ITO Tetsuro
    Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
  • TSURUMA Kazuhiro
    Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
  • ARAKI Yoko
    Nagara Research Center, API Co., Ltd.
  • SHIMAZAWA Masamitsu
    Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University
  • OYAMA Masayoshi
    Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
  • IINUMA Munekazu
    Department of Bioactive Molecules, Pharmacognosy, Gifu Pharmaceutical University
  • HARA Hideaki
    Department of Biofunctional Evaluation, Molecular Pharmacology, Gifu Pharmaceutical University

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タイトル別名
  • Agarwood Induced Laxative Effects via Acetylcholine Receptors on Loperamide-Induced Constipation in Mice

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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.

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