Effect of intraluminal oxygen in intestinal strangulation obstruction in ponies.
Abstract: This study examined the effect of intraluminal oxygen administration on mucosal morphology following intestinal strangulation obstruction (ISO) in anesthetized ponies. The ISO was produced by ligation of the intestinal vasculature in 5 ponies for 50 minutes and 2 ponies for 90 minutes. Two ponies served as controls. Light and scanning electron microscopic examination of intestinal biopsy specimens revealed progressive mucosal degeneration following ISO in nontreated intestines, whereas high magnification scanning electron microscopic examination documented subtle evidence of microvilli disruption 120 minutes following ISO in oxygen-treated intestines.
Publication Date: 1980-10-01 PubMed ID: 7224285
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
- Research Support
- U.S. Gov't
- P.H.S.
Summary
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The research investigated how administrating oxygen in the intestine affected its physical structure after being obstructed in anaesthetized ponies. Findings indicated that oxygen treatment lessened the physical distortion of the intestinal tissue brought by such obstruction.
Methodology
- The research was conducted with a sample size of nine ponies. To simulate intestinal strangulation obstruction (ISO), the researchers constricted the blood flow to the intestines in seven of the ponies. The experiment kept this obstruction for 50 minutes in five ponies and extended to 90 minutes in the other two. Two ponies that were not subjected to ISO served as controls for comparison purposes.
- The researchers administered oxygen into the luminal (inner) space of the intestines in some of the ponies. This method of treatment was key to assessing the effect of oxygen on the deteriorating intestinal tissues.
Observations
- To assess the impact of ISO and oxygen treatment, the researchers performed microscopic examinations of the intestinal tissues. They used light and scanning electron microscopes to visualize the minute changes in the intestinal surface (mucosal) morphology.
- Initial observations were made in non-treated intestines, where the researchers observed progressive mucosal degeneration following ISO. This simply means that the surface layer of the intestinal tissues was seen to break down progressively as a result of the blood supply being cut-off, a condition that simulates ISO.
Results
- Upon observing the intestines in ponies that were given oxygen treatment, however, they found evidence of less drastic damage – subtle disruption in the structure of microvilli (tiny extensions of the cell surface) was noted 120 minutes after the ISO.
- This suggests that delivering oxygen into the obstructed intestine minimized the degree of tissue degradation and retained the structural integrity of the mucosa to some extent. This could possibly hint at a therapeutic strategy for managing intestinal strangulation.
Conclusion
- The experiment concluded that the administration of intraluminal oxygen may have protective effects on intestinal tissue structure during ISO. The less pronounced damage in oxygen-treated intestines, as compared to those not given the treatment, alludes to the beneficial impact of oxygen in preserving microvilli and overall mucosal structure.
- However, more research and verification would be necessary to solidify the findings and understand the therapeutic implications of intraluminal oxygen for ISO treatment in greater depth.
Cite This Article
APA
Moore JN, White NA, Trim CM, Garner HE.
(1980).
Effect of intraluminal oxygen in intestinal strangulation obstruction in ponies.
Am J Vet Res, 41(10), 1615-1620.
Publication
Researcher Affiliations
MeSH Terms
- Animals
- Biopsy
- Horse Diseases / pathology
- Horse Diseases / therapy
- Horses
- Intestinal Obstruction / complications
- Intestinal Obstruction / pathology
- Intestinal Obstruction / veterinary
- Intestines / blood supply
- Ischemia / pathology
- Ischemia / therapy
- Ischemia / veterinary
- Oxygen / therapeutic use
- Time Factors
Grant Funding
- HL05627-02 / NHLBI NIH HHS
Citations
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