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The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats
The traditional Japanese medicine rikkunshito ameliorates the nitric oxide-associated delay in gastric emptying. Whether rikkunshito affects gastric motility associated with 5-hydroxytryptamine (serotonin: 5-HT) receptors or dopamine receptors is unknown. We examined the effects of rikkunshito on th...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095508/ https://www.ncbi.nlm.nih.gov/pubmed/19861508 http://dx.doi.org/10.1093/ecam/nep173 |
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author | Tominaga, K. Kido, T. Ochi, M. Sadakane, C. Mase, A. Okazaki, H. Yamagami, H. Tanigawa, T. Watanabe, K. Watanabe, T. Fujiwara, Y. Oshitani, N. Arakawa, T. |
author_facet | Tominaga, K. Kido, T. Ochi, M. Sadakane, C. Mase, A. Okazaki, H. Yamagami, H. Tanigawa, T. Watanabe, K. Watanabe, T. Fujiwara, Y. Oshitani, N. Arakawa, T. |
author_sort | Tominaga, K. |
collection | PubMed |
description | The traditional Japanese medicine rikkunshito ameliorates the nitric oxide-associated delay in gastric emptying. Whether rikkunshito affects gastric motility associated with 5-hydroxytryptamine (serotonin: 5-HT) receptors or dopamine receptors is unknown. We examined the effects of rikkunshito on the delay in gastric emptying induced by 5-HT or dopamine using the phenol red method in male Wistar rats. 5-HT (0.01–1.0 mg kg(−1), i.p.) dose dependently delayed gastric emptying, similar to the effect of the 5-HT(3) receptor agonist 1-(3-chlorophenyl) biguanide (0.01–1.0 mg kg(−1), i.p.). Dopamine also dose dependently delayed gastric emptying. The 5-HT(3) receptor antagonist ondansetron (0.04–4.0 mg kg(−1)) and rikkunshito (125–500 mg kg(−1)) significantly suppressed the delay in gastric emptying caused by 5-HT or 1-(3-chlorophenyl) biguanide. Hesperidin (the most active ingredient in rikkunshito) suppressed the 5-HT-induced delayed gastric emptying in a dose-dependent manner, the maximum effect of which was similar to that of ondansetron (0.4 mg kg(−1)). The improvement obtained by rikkunshito or ondansetron in delaying gastric emptying was completely blocked by pretreatment with atropine. Rikkunshito appears to improve delay in gastric emptying via the antagonistic action of the 5-HT(3) receptor pathway. |
format | Text |
id | pubmed-3095508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-30955082011-06-17 The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats Tominaga, K. Kido, T. Ochi, M. Sadakane, C. Mase, A. Okazaki, H. Yamagami, H. Tanigawa, T. Watanabe, K. Watanabe, T. Fujiwara, Y. Oshitani, N. Arakawa, T. Evid Based Complement Alternat Med Original Article The traditional Japanese medicine rikkunshito ameliorates the nitric oxide-associated delay in gastric emptying. Whether rikkunshito affects gastric motility associated with 5-hydroxytryptamine (serotonin: 5-HT) receptors or dopamine receptors is unknown. We examined the effects of rikkunshito on the delay in gastric emptying induced by 5-HT or dopamine using the phenol red method in male Wistar rats. 5-HT (0.01–1.0 mg kg(−1), i.p.) dose dependently delayed gastric emptying, similar to the effect of the 5-HT(3) receptor agonist 1-(3-chlorophenyl) biguanide (0.01–1.0 mg kg(−1), i.p.). Dopamine also dose dependently delayed gastric emptying. The 5-HT(3) receptor antagonist ondansetron (0.04–4.0 mg kg(−1)) and rikkunshito (125–500 mg kg(−1)) significantly suppressed the delay in gastric emptying caused by 5-HT or 1-(3-chlorophenyl) biguanide. Hesperidin (the most active ingredient in rikkunshito) suppressed the 5-HT-induced delayed gastric emptying in a dose-dependent manner, the maximum effect of which was similar to that of ondansetron (0.4 mg kg(−1)). The improvement obtained by rikkunshito or ondansetron in delaying gastric emptying was completely blocked by pretreatment with atropine. Rikkunshito appears to improve delay in gastric emptying via the antagonistic action of the 5-HT(3) receptor pathway. Hindawi Publishing Corporation 2011 2011-02-13 /pmc/articles/PMC3095508/ /pubmed/19861508 http://dx.doi.org/10.1093/ecam/nep173 Text en Copyright © 2011 K. Tominaga et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Tominaga, K. Kido, T. Ochi, M. Sadakane, C. Mase, A. Okazaki, H. Yamagami, H. Tanigawa, T. Watanabe, K. Watanabe, T. Fujiwara, Y. Oshitani, N. Arakawa, T. The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title | The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title_full | The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title_fullStr | The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title_full_unstemmed | The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title_short | The Traditional Japanese Medicine Rikkunshito Promotes Gastric Emptying via the Antagonistic Action of the 5-HT(3) Receptor Pathway in Rats |
title_sort | traditional japanese medicine rikkunshito promotes gastric emptying via the antagonistic action of the 5-ht(3) receptor pathway in rats |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095508/ https://www.ncbi.nlm.nih.gov/pubmed/19861508 http://dx.doi.org/10.1093/ecam/nep173 |
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