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Equine veterinary journal2003; 35(5); 472-475; doi: 10.2746/042516403775600488

Effects of lipopolysaccharide and phenylbutazone on gastric contents in the horse.

Abstract: Endotoxaemia causes a disruption of gastrointestinal motility in the horse but there is no information on its effects on gastric secretion. Lipopolysaccharide (LPS) administration is known to affect gastric secretion in other species. Objective: That LPS, a toxic component of Gram-negative bacteria, would reduce gastric acid secretion and that pretreatment with phenylbutazone (PBZ) would block the effects of LPS. Methods: The effects of LPS and PBZ on gastric contents were investigated in fasted, mature horses, with permanent gastric cannulae. Horses were pretreated with either saline or PBZ 15 mins before a 60 min infusion of either LPS or saline. Gastric contents were collected at 15 min intervals for 3 h, beginning 15 mins after the start of the LPS or saline infusion. Results: Lipopolysaccharide significantly decreased gastric acid output, [K+] and potassium output and increased [Na+] and sodium output. Phenylbutazone did not affect basal gastric acid secretion but decreased LPS-induced changes in the secreted volume, [Na+] and sodium output. Conclusions: This study provides evidence that LPS affects gastric acid secretion in the horse and that these LPS-induced changes are mediated, in part, by prostaglandins. Conclusions: Lipopolysaccharide administration can induce changes in the composition of gastric contents in the horse but further work is needed to determine the source of these changes.
Publication Date: 2003-07-24 PubMed ID: 12875325DOI: 10.2746/042516403775600488Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The research explores the effects of lipopolysaccharide (LPS) and phenylbutazone on gastric contents in horses. The hypothesis was that LPS, a toxic element of certain bacteria, would reduce gastric acid secretion and that phenylbutazone could suppress these effects.

Objective and Methods of the Study

The objective of this study was to investigate whether LPS, a toxic component found in Gram-negative bacteria, would impact gastric acid secretion in horses, and to what extent a pretreatment with phenylbutazone could counteract these changes.

  • The study was conducted on mature horses that had fasted and were equipped with permanent gastric cannulae – tubes inserted into their stomachs for medical testing.
  • The horses were pretreated with either saline or phenylbutazone 15 minutes before a one-hour infusion of either LPS or saline.
  • Gastric contents of the horses were collected every 15 minutes for three hours, starting 15 minutes after the LPS or saline infusion had started.

Study Results

The results showed that LPS significantly diminished the output of gastric acid, potassium levels, and potassium output. It also increased sodium levels and sodium output.

  • Phenylbutazone did not affect the base level of gastric acid secretion in the horses.
  • However, it was seen to reduce the changes brought about by LPS in the volume of secreted gastric contents, sodium levels, and sodium output.

Conclusions

The paper provides evidence that LPS does impact the secretion of gastric acid in horses. It also suggests that these changes by LPS are mediated, to some extent, by prostaglandins, a group of physiologically active lipid compounds with hormone-like effects.

  • The researchers concluded that LPS can indeed change the composition of gastric contents in horses.
  • However, the exact source of these changes requires further investigation, indicating the need for additional research in this field.

Cite This Article

APA
Doherty TJ, Andrews FM, Blackford JT, Rohrbach BW, Sandin A, Saxton AM. (2003). Effects of lipopolysaccharide and phenylbutazone on gastric contents in the horse. Equine Vet J, 35(5), 472-475. https://doi.org/10.2746/042516403775600488

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 35
Issue: 5
Pages: 472-475

Researcher Affiliations

Doherty, T J
  • College of Veterinary Medicine, PO Box 1071, The University of Tennessee, Knoxville, Tennessee 37901, USA.
Andrews, F M
    Blackford, J T
      Rohrbach, B W
        Sandin, A
          Saxton, A M

            MeSH Terms

            • Animals
            • Anti-Inflammatory Agents, Non-Steroidal / pharmacology
            • Female
            • Gastric Acid / metabolism
            • Gastrointestinal Contents / chemistry
            • Gastrointestinal Contents / drug effects
            • Horses / physiology
            • Hydrogen-Ion Concentration
            • Lipopolysaccharides / antagonists & inhibitors
            • Lipopolysaccharides / pharmacology
            • Phenylbutazone / pharmacology
            • Potassium / metabolism
            • Random Allocation
            • Sodium / metabolism

            Citations

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