Morphological changes in the small intestinal smooth muscle layers of horses suffering from small intestinal strangulation. Is there a basis for predisposition for reduced contractility?
- Journal Article
Summary
This research explores the morphological changes of small intestinal smooth muscle in horses that suffer from intestinal strangulation and possible connections to a reduced muscle contractility predisposition. It pays primary attention to the presence of some smooth muscle proteins and the regulation of certain heat shock proteins, with findings potentially informing treatments for equine ileus.
Objective and Methodology
The research aimed to explore the presence and quantity of particular smooth muscle proteins in control and colic horses. More specifically, it evaluated the possible up- or down-regulation of heat shock proteins, HSP20 and HSP27, which exert an influence on smooth muscle contractility.
- The method involved collecting cranial resection margins from 18 samples of strangulated small intestines.
- Controlled samples of small intestines were taken from 11 horses, euthanised for non-gastrointestinal reasons.
- Formaldehyde-fixed tissue was paraffin-embedded and processed using conventional staining and immunohistochemistry.
- Snap-frozen full-thickness biopsies were also gathered for western blot analyses.
Findings
Upon microscopic investigation, muscle layers taken from colic horses showed significantly more signs of degradation compared to control samples, with vacuolar degeneration being particularly prominent. Furthermore, myosin protein levels were noticeably reduced in colic samples, while desmin and HSP20 protein levels were found to be elevated.
- These findings suggest that the microscopic damaged observed at the muscle layer level are indicators of a stress response.
- Changes in the amounts of structural proteins such as myosin and desmin, along with heightened HSP20 levels, may provide a rationale for dysfunctional intestinal muscle layers.
Conclusions
The research suggests that postoperative ileus, commonly experienced after small intestinal strangulation and resection, may be partially attributable to a malfunctioning muscle layer.
- Key indicators of this malfunction include observable microscopic signs of degeneration, and the altered presence of both myosin and HSP20 proteins.
- The study recommends potential pharmacological interventions aiming at adjusting HSP20 expressions, which may accordingly offer a protective effect for vulnerable horses.
Cite This Article
Publication
Researcher Affiliations
- Department of Veterinary Sciences, Laboratory of Veterinary Anatomy, Embryology and Pathology, University of Antwerp, Belgium.
MeSH Terms
- Animals
- Biopsy / veterinary
- Blotting, Western
- Colic / metabolism
- Colic / pathology
- Colic / veterinary
- Female
- HSP20 Heat-Shock Proteins / metabolism
- HSP27 Heat-Shock Proteins / metabolism
- Horse Diseases / metabolism
- Horse Diseases / pathology
- Horses
- Immunohistochemistry / veterinary
- Intestinal Diseases / metabolism
- Intestinal Diseases / pathology
- Intestinal Diseases / veterinary
- Intestine, Small / metabolism
- Intestine, Small / pathology
- Male
- Muscle Contraction / physiology
- Muscle, Smooth / metabolism
- Muscle, Smooth / pathology
- Muscle, Smooth / ultrastructure
- Myosins / metabolism
- Statistics, Nonparametric
Citations
This article has been cited 3 times.- Bardell D, Rocchigiani G, Ressel L, Milner P. Histological Evaluation of Resected Tissue as a Predictor of Survival in Horses with Strangulating Small Intestinal Disease.. Animals (Basel) 2023 Aug 26;13(17).
- Dengler F, Sternberg F, Grages M, Kästner SB, Verhaar N. Adaptive mechanisms in no flow vs. low flow ischemia in equine jejunum epithelium: Different paths to the same destination.. Front Vet Sci 2022;9:947482.
- Ohlsson L, Isaxon C, Wrighton S, El Ouahidi W, Fornell L, Uller L, Ansar S, Voss U. Short-term exposure to urban PM(2.5) particles induces histopathological and inflammatory changes in the rat small intestine.. Physiol Rep 2022 Apr;10(7):e15249.