Modifications of capsaicin-sensitive neurons in isolated guinea pig ileum by [6]-gingerol and lafutidine |
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Authors: | Someya Akiyoshi Horie Shunji Yamamoto Hisashi Murayama Toshihiko |
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Institution: | Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, Chiba University, Chiba, Japan. |
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Abstract: | A segment of guinea pig ileum was used to confirm the hypothesis that 6]-gingerol and lafutidine interact with capsaicin-sensitive neurons. Addition of 30 and 100 microM 6]-gingerol (a pungent constituent of ginger) induced contraction of the ileum immediately. Like capsaicin, 6]-gingerol-induced contraction was inhibited by antagonists of the vanilloid receptor (capsazepine and ruthenium red), tetrodotoxin, and atropine. Treatment with 6]-gingerol up to 0.3 microM, which alone had no effect, enhanced 3 microM capsaicin-induced contraction, but greater than 3 microM 6]-gingerol significantly inhibited capsaicin-induced contraction. Treatment with lafutidine (a new type of antagonist of the histamine H(2) receptor), which was suggested to interact with capsaicin-sensitive neurons in vivo, also showed both stimulatory and inhibitory effects on capsaicin-induced contraction depending on the concentrations. Lafutidine alone had no effect. The enhanced contraction induced by capsaicin in the 6]-gingerol- or lafutidine-treated ileum was also inhibited by antagonists of the vanilloid receptor, tetrodotoxin, and atropine. Capsaicin and 6]-gingerol, but not lafutidine, at 30 microM stimulated (3)H]choline release from the prelabeled slices of the ileum. These findings suggest that 6]-gingerol and lafutidine act on capsaicin-sensitive cholinergic neurons and modulate the contraction in isolated guinea pig ileum. |
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