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Equine veterinary journal1981; 13(2); 95-98; doi: 10.1111/j.2042-3306.1981.tb04122.x

Prevention of endotoxin-induced arterial hypoxaemia and lactic acidosis with flunixin meglumine in the conscious pony.

Abstract: Bacterial endotoxin injected intravenously into conscious ponies produced alterations in cardiopulmonary and gastrointestinal function. Specifically, tachypnoea, dyspnoea, hypoxaemia, colic, lactic acidosis and diarrhoea resulted from administration of 10 micrograms/kg Escherichia coli endotoxin. Pretreatment of the ponies with a potent prostaglandin synthetase inhibitor, flunixin meglumine, prevented these ill effects of endotoxin.
Publication Date: 1981-04-01 PubMed ID: 7018898DOI: 10.1111/j.2042-3306.1981.tb04122.xGoogle Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article studies how flunixin meglumine can prevent problems such as rapid breathing, diarrhea, colic, or hypoxaemia induced by endotoxins in conscious ponies.

Objective of the Research

  • The study aimed to investigate the possibility of preventing the negative effects that result from an intravenous injection of bacterial endotoxin in conscious ponies by using the drug flunixin meglumine.

Methodology and Experimental Setup

  • The researchers injected Escherichia coli endotoxin intravenously into conscious ponies. The dosage was 10 micrograms per kilogram.
  • The effect of the endotoxin administration led to various conditions like tachypnoea (fast breathing), dyspnoea (shortness of breath), hypoxaemia (low oxygen level in the blood), colic (abdominal pain), lactic acidosis (build-up of lactic acid more than it can be gotten rid of), and diarrhoea.
  • To ascertain if these conditions could be prevented, the researchers pre-treated the ponies with the drug flunixin meglumine, a potent prostaglandin synthetase inhibitor, before administering the endotoxin.

Findings and Conclusions

  • The findings demonstrated that flunixin meglumine was able to prevent the ill effects that resulted from the administration of endotoxin. This suggests that this drug might be useful in preventing the development of these conditions when endotoxin enters the bloodstream of conscious ponies.
  • In a broader sense, it may imply the potential use of flunixin meglumine or similar drugs in preventing the detrimental effects of other toxins or infections in other animals or even humans.
  • The findings need to be corroborated with larger sample sizes and possibly other species to get a better understanding of its potential in clinical applications.

Cite This Article

APA
Moore JN, Garner HE, Shapland JE, Hatfield DG. (1981). Prevention of endotoxin-induced arterial hypoxaemia and lactic acidosis with flunixin meglumine in the conscious pony. Equine Vet J, 13(2), 95-98. https://doi.org/10.1111/j.2042-3306.1981.tb04122.x

Publication

ISSN: 0425-1644
NlmUniqueID: 0173320
Country: United States
Language: English
Volume: 13
Issue: 2
Pages: 95-98

Researcher Affiliations

Moore, J N
    Garner, H E
      Shapland, J E
        Hatfield, D G

          MeSH Terms

          • Acidosis / prevention & control
          • Acidosis / veterinary
          • Animals
          • Bicarbonates / blood
          • Blood Gas Analysis / veterinary
          • Carotid Arteries
          • Clonixin / administration & dosage
          • Clonixin / analogs & derivatives
          • Clonixin / therapeutic use
          • Endotoxins
          • Escherichia coli
          • Horse Diseases / prevention & control
          • Horses
          • Hypoxia / prevention & control
          • Hypoxia / veterinary
          • Lactates / blood
          • Meglumine / administration & dosage
          • Meglumine / analogs & derivatives
          • Meglumine / therapeutic use
          • Nicotinic Acids / therapeutic use

          Grant Funding

          • USPH 5 F32 HL 05627-02 / NHLBI NIH HHS

          Citations

          This article has been cited 12 times.
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            pubmed: 2713784