Perilla ketone toxicity: a chemical model for the study of equine restrictive lung disease.
Abstract: Perilla ketone was assessed for its usefulness as a model of equine restrictive pulmonary disease. Three ponies were given 18 mg/kg bodyweight synthetic perilla ketone in dimethyl-sulphoxide. Within 24 h of administration, respiratory rate, peak inspiratory and expiratory flow rates and minute volume were increased. By 48 h there was a significant decrease in tidal volume, and blood pH and base excess were also decreased but not outside normal limits. At necropsy there was congestion and oedema of the lungs. Histologically there was diffuse alveolar injury but no evidence of significant obstruction in bronchial or bronchiolar lumina. It is assumed that perilla ketone toxicity in ponies produces a restrictive disease without a significant obstructive component.
Publication Date: 1984-05-01 PubMed ID: 6734583DOI: 10.1111/j.2042-3306.1984.tb01897.xGoogle Scholar: Lookup
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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The research studied the effects of perilla ketone on the respiration of ponies to model equine restrictive lung disease, with results indicating changes in respiratory characteristics and physical conditions, but without significant obstruction of airways.
Introduction to the Research
- The paper discusses a restrictive lung disease study in horses using a chemical model, specifically, perilla ketone. The key focus was to explore the usefulness of this ketone as a model for equine restrictive pulmonary disease.
- The study was conducted on three different ponies, and they were administered a synthetic perilla ketone to monitor the effects on their respiratory systems.
- The dosage given was uniform and calculated to be 18 mg/kg of the body weight, using dimethyl-sulphoxide as a solvent.
Results and Analysis
- Within 24 hours of administering the synthetic perilla ketone, indicators of pulmonary function, such as respiratory rate, peak inspiratory and expiratory flow rates, and minute volume, were recorded and showed an increase.
- As the study progressed, by the end of 48 hours, a significant decrease in tidal volume appeared, along with decreases in blood pH and base excess. However, these decreases were not extreme enough to fall outside normal limits.
- The ponies also underwent a necropsy, a post-mortem examination, which revealed congestion and oedema in their lungs as a result of the perilla ketone administration.
- A histological analysis of the lung tissue displayed signs of widespread alveolar injury but importantly, it showed no evidence of significant obstruction within their respiratory bronchial or bronchiolar lumina. This is consistent with the restrictive nature of pulmonary diseases as opposed to obstructive ones.
Conclusion and Assumptions
- The researchers concluded based on their observations that perilla ketone toxicity in ponies produces a condition that closely mirrors a restrictive lung disease, but importantly, without a significant obstructive component.
- This is a key finding because this restrictive disease model without an obstructive component could be used in further studies about restrictive lung diseases in horses, providing crucial insights into disease mechanisms and potential therapeutic strategies.
Cite This Article
APA
Breeze RG, Legreid WW, Bayly WM, Wilson BJ.
(1984).
Perilla ketone toxicity: a chemical model for the study of equine restrictive lung disease.
Equine Vet J, 16(3), 180-184.
https://doi.org/10.1111/j.2042-3306.1984.tb01897.x Publication
Researcher Affiliations
MeSH Terms
- Animals
- Dimethyl Sulfoxide / pharmacology
- Disease Models, Animal
- Horse Diseases / chemically induced
- Horse Diseases / physiopathology
- Horses
- Lung / drug effects
- Lung / physiopathology
- Lung Diseases, Obstructive / chemically induced
- Lung Diseases, Obstructive / physiopathology
- Lung Diseases, Obstructive / veterinary
- Monoterpenes
- Respiratory Function Tests / veterinary
- Terpenes / toxicity
Citations
This article has been cited 3 times.- Röder A, Hüsken S, Hutter MC, Rettie AE, Hanenberg H, Wiek C, Girhard M. Spotlight on CYP4B1. Int J Mol Sci 2023 Jan 20;24(3).
- Roellecke K, Jäger VD, Gyurov VH, Kowalski JP, Mielke S, Rettie AE, Hanenberg H, Wiek C, Girhard M. Ligand characterization of CYP4B1 isoforms modified for high-level expression in Escherichia coli and HepG2 cells. Protein Eng Des Sel 2017 Mar 1;30(3):205-216.
- Asin J, Carvallo F, Gonzales-Viera OA, Macías-Rioseco M, Streitenberger N, Abdelrazek S, Crossley B, Pesavento PA, Uzal FA. Interstitial pneumonias of undetermined etiology in foals in California, 1990-2020. J Vet Diagn Invest 2026 Jan 29;:10406387251410524.
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