Inhaled Pinacidil, an ATP-Sensitive K+ Channel Opener, and Moguisteine Have Potent Antitussive Effects in Guinea Pigs.

  • Morita Kayo
    Department of Pathophysiology & Therapeutics, Faculty of Pharmaceutical Sciences, Hoshi University
  • Onodera Kenji
    Department of Dental Pharmacology, Okayama University Graduate School of Medicine and Dentistry
  • Kamei Junzo
    Department of Pathophysiology & Therapeutics, Faculty of Pharmaceutical Sciences, Hoshi University

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We investigated whether inhaled pinacidil and moguisteine inhibit capsaicin-induced coughs in guinea pigs. Inhaled pinacidil (15 – 60 μg/ml), an ATP-sensitive K+ channel opener, and moguisteine (15 – 60 μg/ml) each dose-dependently inhibited the number of capsaicin-induced coughs. The antitussive effects of pinacidil and moguisteine were significantly antagonized by pretreatment with glibenclamide (10 mg/kg, i.p.), an ATP-sensitive K+ channel blocker. However, pretreatment with naloxone methiodide (10 mg/kg, s.c.) had no significant effect on the antitussive effects of either pinacidil or moguisteine. On the other hand, inhaled dihydrocodeine (15 – 60 μg/ml) also dose-dependently suppressed the number of capsaicin-induced coughs. The antitussive effect of inhaled dihydrocodeine was significantly antagonized by pretreatment with naloxone methiodide (10 mg/kg, s.c.), but not by glibenclamide (10 mg/kg, i.p.). These results indicate that inhaled pinacidil and moguisteine both attenuate capsaicin-induced coughs. Pinacidil and moguisteine may exert their antitussive effects through the activation of ATP-sensitive K+ channels in the tracheobronchial tract. Furthermore, it is possible that ATP-sensitive K+ channels may be involved in the antitussive effects of peripherally acting non-narcotic antitussive drugs.

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  • Jpn.J.Pharmacol.

    Jpn.J.Pharmacol. 89 (2), 171-175, 2002

    公益社団法人 日本薬理学会

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