Beta-adrenergic blockade in ponies with recurrent obstructive pulmonary disease.
Abstract: Ponies with recurrent airway obstruction have hyperresponsive airways during acute disease exacerbations but not during clinical remission. We examined the effect of beta-adrenergic blockade with propranolol on airway responsiveness to aerosol histamine in six ponies with recurrent airway obstruction and six age- and gender-matched controls. Measurements were made with principal ponies in clinical remission (period A) and during an acute period of airway obstruction (period B). beta-Adrenergic blockade did not change airway responsiveness, dynamic compliance (Cdyn), or pulmonary resistance (RL) in either group of ponies at period A or in the control ponies at period B. In principal ponies at period B, propranolol significantly increased RL but was without effect on Cdyn or airway responsiveness. We conclude that the beta-adrenergic system is involved in the control of central airway caliber in principal ponies at period B but that this system does not seem to be involved in the mechanism of airway hyperresponsiveness to histamine.
Publication Date: 1988-06-01 PubMed ID: 2841272DOI: 10.1152/jappl.1988.64.6.2324Google 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
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This research studied the effect of a drug called propranolol on ponies suffering from a recurrent airway obstruction. It found that while the drug increased pulmonary resistance during periods of acute disease, it did not appear to play a significant role in the airway’s hyperresponsiveness to histamine.
Introduction and Methodology
- This research was conducted on twelve ponies, half of which were suffering from Recurrent Airway Obstruction (RAO), a chronic breathing difficulty somewhat similar to asthma in humans. The other half served as age- and gender-matched control subjects.
- Measurements were made at two different periods – during clinical remission (Period A) and during an acute phase of airway obstruction (Period B).
- The researchers used beta-adrenergic blockade, a type of therapy that involves the use of propranolol, a medication often used to treat high blood pressure and heart conditions. The medication was used to study its effects on the airway responsiveness to aerosol histamine, a compound which can cause narrowing of the airways and difficulty in breathing.
Results and Discussion
- The study found that the propranolol medication did not change the airway responsiveness, dynamic compliance (Cdyn – a measure of lung elasticity), or pulmonary resistance (RL – a measure of the resistance to airflow in the respiratory tract) in the control group or in the RAO ponies during clinical remission (Period A).
- However, during the period of acute disease (Period B), the administration of propranolol significantly increased pulmonary resistance in the affected ponies, suggesting a worsening of their airway obstruction.
- Despite this, the drug had no effect on the lung’s dynamic compliance or on the airway’s responsiveness to the histamine aerosol.
Conclusion
- From these results, the researchers concluded that the beta-adrenergic system, which is affected by propranolol, seems to be involved in controlling the size of the airway in RAO ponies during acute disease periods. They also inferred that this system does not seem to play a significant role in the airway’s overreaction to histamine.
- However, further research is needed to confirm and better understand these findings, especially since the beta-adrenergic system’s role in airway obstruction remains significantly unexplored.
Cite This Article
APA
Scott JS, Broadstone RV, Derksen FJ, Robinson NE.
(1988).
Beta-adrenergic blockade in ponies with recurrent obstructive pulmonary disease.
J Appl Physiol (1985), 64(6), 2324-2328.
https://doi.org/10.1152/jappl.1988.64.6.2324 Publication
Researcher Affiliations
- Pulmonary Laboratory, College of Veterinary Medicine, Michigan State University, East Lansing 48824.
MeSH Terms
- Airway Resistance / drug effects
- Animals
- Horse Diseases / physiopathology
- Horses
- Lung / drug effects
- Lung / physiology
- Lung / physiopathology
- Lung Compliance / drug effects
- Lung Diseases, Obstructive / physiopathology
- Lung Diseases, Obstructive / veterinary
- Propranolol / pharmacology
- Receptors, Adrenergic, beta / drug effects
- Receptors, Adrenergic, beta / physiology
- Reference Values
Grant Funding
- HL-01455 / NHLBI NIH HHS
- HL-27619 / NHLBI NIH HHS
Citations
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