Effects of Carolina rinse solution, dimethyl sulfoxide, and the 21-aminosteroid, U-74389G, on microvascular permeability and morphology of the equine jejunum after low-flow ischemia and reperfusion.
Abstract: To evaluate effects of Carolina rinse solution, dimethyl sulfoxide (DMSO), and 21-aminosteroid, U-74389G, on microvascular permeability and morphology of the equine jejunum after low-flow ischemia and reperfusion. Methods: 20 healthy adult horses. Methods: Under anesthesia, full-thickness biopsy specimens of a distal portion of the jejunum were obtained for baseline measurements. In addition to a control segment, 2 jejunal segments were identified as sham-operated or experimental segments. Experimental segments underwent 60 minutes of low-flow ischemia and 3.5 hours of reperfusion. Treatments were as follows: U-74389G (3 mg/kg, IV; 6 horses), DMSO (20 mg/kg, IV; 6) diluted in 1 L of saline (0.9% NaCl) solution, local perfusion (via jejunal artery) of Carolina rinse solution (0.5 mL/kg; 4), and local perfusion of lactated Ringer's solution (0.5 mL/kg; 4). Results: Jejunal microvascular permeability was significantly lower after treatment with Carolina rinse solution or DMSO, compared with U-74389G or lactated Ringer's solution treatments. After DMSO treatment, serosal- and submucosal-layer edema was significantly increased in experimental segments, compared with control or sham-operated segments; however, edema increases were significantly less than for lactated Ringer's solution or U-74389G treatments. Significant decreases in intestinal wet weight-to-dry weight ratio were found following Carolina rinse solution or DMSO treatments, compared with lactated Ringer's solution or U-74389G treatments. Edema formation and leukocyte infiltration in jejunal segments of horses treated with lactated Ringer's solution or U-74389G were increased, compared with Carolina rinse solution or DMSO treatments. Conclusions: Carolina rinse solution and DMSO may be protective against ischemia-reperfusion injury in the equine jejunum.
Publication Date: 2005-04-13 PubMed ID: 15822599DOI: 10.2460/ajvr.2005.66.525Google Scholar: Lookup
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- Comparative Study
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research article evaluates how treatments with Carolina rinse solution, dimethyl sulfoxide (DMSO), and 21-aminosteroid (U-74389G) affect the microvascular permeability and morphology of a horse’s small intestine (jejunum) after undergoing low-flow ischemia and reperfusion – a process mimicking conditions of interrupted blood supply.
Research Methodology
- The research was conducted on 20 healthy adult horses under anesthesia. Full-thickness biopsy samples of a distal portion of the jejunum were taken for baseline measurements.
- Segments of the jejunum underwent 60 minutes of low-flow ischemia (restricted blood flow) and 3.5 hours of reperfusion (restoration of blood flow).
Treatments
- The horses were randomly split into groups for treatment with one of the three substances being tested. U-74389G was administered intravenously (IV) to 6 horses, DMSO (also IV) was given to another 6 horses, Carolina rinse solution was locally perfused to 4 horses, and the remaining four horses were perfused with a lactated Ringer’s solution to serve as a control group.
Results
- The researchers found that microvascular permeability of the jejunum was significantly lower after treatment with Carolina rinse solution or DMSO, when compared to the horses treated with U-74389G or the lactated Ringer’s solution.
- After DMSO treatment, there was a significant increase in edema (swelling) in the layers of the jejunum in the treatment group, but the increase was significantly less than for those treated with lactated Ringer’s solution or U-74389G.
- There were significant decreases in intestinal wet weight-to-dry weight ratio following treatments with Carolina rinse solution or DMSO, compared with lactated Ringer’s solution or U-74389G treatments.
- Horses treated with lactated Ringer’s solution or U-74389G had increased edema formation and leukocyte (white blood cell) infiltration in their jejunal segments compared to those treated with Carolina rinse solution or DMSO.
Conclusions
- The researchers concluded that both the Carolina rinse solution and DMSO might provide protection against the damage caused by ischemia-reperfusion in the horse’s jejunum, a process that can simulate situations such as recovery from shock or a surgical procedure.
Cite This Article
APA
Dabareiner RM, White NA, Snyder JR, Feldman BF, Donaldson LL.
(2005).
Effects of Carolina rinse solution, dimethyl sulfoxide, and the 21-aminosteroid, U-74389G, on microvascular permeability and morphology of the equine jejunum after low-flow ischemia and reperfusion.
Am J Vet Res, 66(3), 525-536.
https://doi.org/10.2460/ajvr.2005.66.525 Publication
Researcher Affiliations
- Marion DuPont Scott Equine Medical Center, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Leesburg, VA 20177, USA.
MeSH Terms
- Animals
- Body Weights and Measures / veterinary
- Capillary Permeability / drug effects
- Dimethyl Sulfoxide / pharmacology
- Horse Diseases / physiopathology
- Horse Diseases / prevention & control
- Horses
- Jejunum / blood supply
- Jejunum / drug effects
- Jejunum / ultrastructure
- Microscopy, Electron, Transmission / veterinary
- Pregnatrienes / pharmacology
- Reperfusion Injury / prevention & control
- Reperfusion Injury / veterinary
- Solutions / pharmacology
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).
- Sasaki M, Joh T. Oxidative stress and ischemia-reperfusion injury in gastrointestinal tract and antioxidant, protective agents.. J Clin Biochem Nutr 2007 Jan;40(1):1-12.
- Faleiros RR, Macoris DG, Alves GE, Souza DG, Teixeira MM, Moore RM. Local and remote lesions in horses subjected to small colon distension and decompression.. Can J Vet Res 2008 Jan;72(1):68-76.
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