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American journal of veterinary research2005; 66(8); 1321-1323; doi: 10.2460/ajvr.2005.66.1321

Effects of mosapride, a 5-hydroxytryptamine 4 receptor agonist, on electrical activity of the small intestine and cecum in horses.

Abstract: To examine the effects of various doses of mosapride, a 5-hydroxytryptamine 4 receptor agonist, on motility of the small intestine and cecum in horses by use of electrical activity and to determine the dose that provides the optimal response. Methods: 6 healthy adult Thoroughbreds. Methods: Electrical activity of the small intestine and cecum was recorded before and after mosapride administration by use of an electrogastrograph. Mosapride (0.5, 1, 1.5, and 2 mg/kg) was dissolved in 200 mL of water and administered orally to horses through a nasogastric tube. Three hours after drug administration, mean amplitude of electrical activity calculated for a period of 30 minutes was expressed as the percentage of the mean amplitude of electrical activity for a period of 30 minutes before drug administration. Results: Mosapride administered orally increased the percentage of the mean amplitude of electrical activity in the small intestine and cecum in a dose-dependent manner. Mean +/- SD values differed significantly for 1, 1.5, and 2 mg/kg (127.0 +/- 12.5%, 137.7 +/- 22.2%, and 151.1 +/- 24.0%, respectively) in the small intestine and for 1.5 and 2 mg/kg (130.1 +/- 34.5% and 151.6 +/- 45.2%, respectively) in the cecum. Conclusions: Analysis of results of this study clearly documents that mosapride promotes motility in the small intestine and cecum of horses and that the optimal orally administered dosage is 1.5 to 2 mg/kg. Therefore, mosapride may be useful for treatment of horses with gastrointestinal tract dysfunction.
Publication Date: 2005-09-22 PubMed ID: 16173472DOI: 10.2460/ajvr.2005.66.1321Google Scholar: Lookup
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  • Journal Article

Summary

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This research studied the effect of varied doses of mosapride, a drug, on the motility of the small intestine and cecum in horses. It found that mosapride stimulates motility in these organs, suggesting potential usefulness in treating horses with gastrointestinal dysfunction.

Introduction and Methods

  • The study aimed to understand the impact of mosapride on the intestines’ electrical activity in horses. Mosapride is an agonist for the 5-hydroxytryptamine 4 receptor.
  • The researchers experimented with different doses of the drug and analyzed the effect to find the dosage for optimal response.
  • The subject pool consisted of six healthy adult Thoroughbreds. The horses’ intestinal and cecum electrical activity was recorded before and after the administration of mosapride.
  • Mosapride was dissolved in water and given orally through a nasogastric tube in doses of 0.5, 1, 1.5 and 2 mg/kg.
  • The mean amplitude of electrical activity post three hours of drug administration was calculated and expressed as a percentage of the mean amplitude before drug administration.

Results

  • The results indicated an increase in the electrical activity in the intestines and cecum. This indicated that mosapride stimulated increased motility in these organs.
  • This percentage increase was found to be dose-dependent, with higher doses resulting in greater effects.
  • Specifically, doses of 1, 1.5 and 2 mg/kg caused significant increases in the small intestine, while doses of 1.5 and 2 mg/kg effected significant increases in the cecum.

Conclusion

  • The analysis documented that mosapride promotes motility in the small intestines and cecum of horses, with the optimal dosage being 1.5 to 2 mg/kg when administered orally.
  • The results of the study highlight the potential benefits of mosapride for treating gastrointestinal tract dysfunction in horses.

Cite This Article

APA
Sasaki N, Okamura K, Yamada H. (2005). Effects of mosapride, a 5-hydroxytryptamine 4 receptor agonist, on electrical activity of the small intestine and cecum in horses. Am J Vet Res, 66(8), 1321-1323. https://doi.org/10.2460/ajvr.2005.66.1321

Publication

ISSN: 0002-9645
NlmUniqueID: 0375011
Country: United States
Language: English
Volume: 66
Issue: 8
Pages: 1321-1323

Researcher Affiliations

Sasaki, Naoki
  • Department of Veterinary Surgery, Obihiro University of Agriculture and Veterinary Medicine, Inada, Obihiro, Hokkaido, 080-8555, Japan.
Okamura, Kouichi
    Yamada, Haruo

      MeSH Terms

      • Animals
      • Benzamides / pharmacology
      • Cecum / drug effects
      • Cecum / physiology
      • Dose-Response Relationship, Drug
      • Electrophysiology
      • Gastrointestinal Motility / drug effects
      • Horses / physiology
      • Intestine, Small / drug effects
      • Intestine, Small / physiology
      • Morpholines / pharmacology
      • Serotonin 5-HT4 Receptor Agonists

      Citations

      This article has been cited 5 times.
      1. Arai S, Haritani M, Sawada H, Kimura K. Effect of mosapride on ruminal motility in cattle. J Vet Med Sci 2019 Jul 19;81(7):1017-1020.
        doi: 10.1292/jvms.19-0196pubmed: 31155551google scholar: lookup
      2. Lee JW, Sung KW, Lee OY, Lee SE, Sohn CI. The effects of 5-HT4 receptor agonist, mosapride citrate, on visceral hypersensitivity in a rat model. Dig Dis Sci 2012 Jun;57(6):1517-24.
        doi: 10.1007/s10620-012-2101-zpubmed: 22427128google scholar: lookup
      3. Okamura K, Sasaki N, Kikuchi T, Murata A, Lee I, Yamada H, Inokuma H. Effects of mosapride on motility of the small intestine and caecum in normal horses after jejunocaecostomy. J Vet Sci 2009 Jun;10(2):157-60.
        doi: 10.4142/jvs.2009.10.2.157pubmed: 19461212google scholar: lookup
      4. Prause AS, Stoffel MH, Portier CJ, Mevissen M. Expression and function of 5-HT7 receptors in smooth muscle preparations from equine duodenum, ileum, and pelvic flexure. Res Vet Sci 2009 Oct;87(2):292-9.
        doi: 10.1016/j.rvsc.2009.03.009pubmed: 19364615google scholar: lookup
      5. Kong J, Wu SD, Zhang XB, Li ZS, Shi G, Wang W, Chen JZ. Choledochoscope manometry about different drugs on the Sphincter of Oddi. World J Gastroenterol 2008 Oct 14;14(38):5907-12.
        doi: 10.3748/wjg.14.5907pubmed: 18855992google scholar: lookup