JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Weissberg, R. M.
Right arrow Articles by Bradshaw, J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Weissberg, R. M.
Right arrow Articles by Bradshaw, J.

Respiratory and cardiovascular effects of prostaglandins in the conscious guinea pig

RM Weissberg, J Marian and J Bradshaw

A technique to assess respiratory and cardiovascular effects of prostaglandins (PGs) in conscious guinea pigs was developed. Animals were placed in a plethysmograph and tidal volume, airflow, and heart rate were recorded. In addition, blood pressure and/or pleural pressure were obtained. Some experiments involved the use of a pulmonary calculator that processed the appropriate pulmonary signal and provided on-line readout of dynamic compliance and airway resistance. Aerosolized antagonists were evaluated for their ability to block responses to aerosolized histamine. We found the relative antagonistic potencies of PGE1, PGE2, isoproterenol, and salbutamol to be 5.5, 2.3, 1 and 0.2, respectively. Aerosolized PGE1 and PGE2 but not PGF2alpha given prior to histamine caused decreases in tidal volume, airflow and heart rate. These effects were not seen in animals that were prepared for measurements involving invasive surgical techniques. The aerosolized PGE2 induced tidal volume changes were not prevented by pretreatment with salbutamol, chlorpheniramine, atropine or hexamethonium, though the latter two drugs inhibited the fall in heart rate. We suggest that the bradycardia following aerosolized PGE2 administration may originate from airway irritant receptors. The results validate use of our methods for the assessment of responses to bronchoactive agents under physiological conditions.

Volume 198, Issue 1, pp. 197-208, 07/01/1976
Copyright © 1976 by American Society for Pharmacology and Experimental Therapeutics







Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1976 by the American Society for Pharmacology and Experimental Therapeutics.