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 HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Christensen, J.
Right arrow Articles by Daniel, E. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Christensen, J.
Right arrow Articles by Daniel, E. E.
Journal of Pharmacology And Experimental Therapeutics, Vol. 159, Issue 2, 243-249, 1968
Copyright © 1968 by American Society for Pharmacology and Experimental Therapeutics


EFFECTS OF SOME AUTONOMIC DRUGS ON CIRCULAR ESOPHAGEAL SMOOTH MUSCLE

J. Christensen 1 and E. E. Daniel 1

1 Department of Internal Medicine, University of Iowa, Iowa City, Iowa and Department of Pharmacology, University of Alberta, Edmonton, Alberta, Canada

Strips from the lowest centimeter of the cat esophagus were mounted to record tension and electrical activity in the circular muscle. There were no spontaneous contractions. Slow waves and spike bursts were absent in resting tissue but occurred during drug-induced activity. Cholinergic drugs produced contractions. Maximal responses to acetylcholine were less than those to methacholine and carbachol. Norepinephrine produced contractions opposed by tolazoline but not by propranolol. Contractile responses to the cholinergic drugs and to norepinephrine were opposed by atropine but were not altered by nicotine or hexamethonium. Responses to the four stimulating drugs declined slowly with time and tachyphylaxis was not apparent. Isoproterenol had no stimulating effect but depressed the contractile responses to cholinergic drugs. The degree of depression was dose-related. The effect was opposed by propranolol. Similar depression could be shown from norepinephrine and epinephrine in the presence of tolazoline. Thus, adrenergic alpha receptors in this tissue are excitatory and beta receptors inhibitory. Cholinergic drugs are excitatory. Relaxation of the lower esophageal sphincter, if mediated through adrenergic nerves, is a response to the stimulation of adrenergic beta receptors.

Submitted on August 21, 1967
Accepted on October 23, 1967




This article has been cited by other articles:


Home page
Am. J. Physiol. Gastrointest. Liver Physiol.Home page
H. G. Preiksaitis and N. E. Diamant
Myogenic mechanism for peristalsis in the cat esophagus
Am J Physiol Gastrointest Liver Physiol, August 1, 1999; 277(2): G306 - G313.
[Abstract] [Full Text] [PDF]




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

Copyright © 1968 by the American Society for Pharmacology and Experimental Therapeutics.