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Beta-adrenergic blockade in ponies with recurrent obstructive pulmonary disease
J S Scott1, R V Broadstone, F J Derksen
1Pulmonary Laboratory, College of Veterinary Medicine, Michigan State University, East Lansing 48824.
Journal of Applied Physiology (Bethesda, Md. : 1985)
|June 1, 1988
Summary
Beta-adrenergic blockade did not affect airway hyperresponsiveness in ponies with recurrent airway obstruction. Propranolol increased pulmonary resistance during acute obstruction, suggesting beta-adrenergic involvement in central airway caliber control.
Area of Science:
- Veterinary Medicine
- Respiratory Physiology
- Pharmacology
Background:
- Recurrent airway obstruction (RAO) in ponies is characterized by airway hyperresponsiveness during exacerbations.
- The role of the beta-adrenergic system in RAO pathophysiology remains unclear.
Purpose of the Study:
- To investigate the effect of beta-adrenergic blockade using propranolol on airway responsiveness in ponies with RAO.
- To determine if the beta-adrenergic system influences airway hyperresponsiveness or airway caliber during remission and exacerbation phases of RAO.
Main Methods:
- Six ponies with RAO and six controls received aerosol histamine challenges before and after propranolol administration.
- Measurements included airway responsiveness, dynamic compliance (Cdyn), and pulmonary resistance (RL).
- Studies were conducted during clinical remission (Period A) and acute airway obstruction (Period B).
Main Results:
- Propranolol did not alter airway responsiveness, Cdyn, or RL in either group during remission (Period A).
- In RAO ponies during acute obstruction (Period B), propranolol significantly increased RL but did not affect Cdyn or airway responsiveness.
- Control ponies showed no significant changes after propranolol administration in Period B.
Conclusions:
- The beta-adrenergic system plays a role in regulating central airway caliber in RAO ponies during acute exacerbations.
- Beta-adrenergic blockade does not appear to be involved in the mechanism of histamine-induced airway hyperresponsiveness in RAO ponies.