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 PRIANO, L. L.
Right arrow Articles by WILSON, R. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by PRIANO, L. L.
Right arrow Articles by WILSON, R. D.
Right arrowPubmed/NCBI databases
*Compound via MeSH
*Substance via MeSH
Hazardous Substances DB
*2-BROMO-2-CHLORO-1,1,1-TRIFLUOROETHANE
*CARBON DIOXIDE
*OXYGEN
*PENTOBARBITAL
Journal of Pharmacology And Experimental Therapeutics, Vol. 165, Issue 1, 126-135, 1969
Copyright © 1969 by American Society for Pharmacology and Experimental Therapeutics


BARBITURATE ANESTHESIA: AN ABNORMAL PHYSIOLOGIC SITUATION

L. L. PRIANO 1, D. L. TRABER 1, and R. D. WILSON 1

1 Departments of Physiology and Anesthesiology, The University of Texas Medical Branch and Shriners Burns Institute, Galveston, Texas

The cardiovascular responses to an anesthetic dose of pentobarbital were examined in unpremedicated, unanesthetized dogs. Catheter implantations and electrocardiograph electrode placement were performed under halothane anesthesia. Full recovery of the animal was allowed, after which unanesthetized controls were taken. Variables measured included systolic, diastolic and mean arterial blood pressures, central venous pressure, heart rate, initial ventricular impulse, cardiac output and arterial pO2 , pCO2 and pH. Stroke volume, pulse pressure and total peripheral resistance were calculated. Sodium pentobarbital (30 mg/kg) was then administered i.v. After stabilization, the cardiovascular responses were recorded at frac12-hr intervals for a 2frac12-hr period. Systolic blood pressure remained significantly depressed throughout the test period as did the initial ventricular impulse, stroke volume, pulse pressure, central venous pressure, pO2, pH and body temperature. Heart rate and pCO2 remained statistically significantly greater than control. Mean blood pressure showed only one significant change from control, that being a decrease. The peripheral resistance was significantly elevated from 1frac12 hr on, and cardiac output had decreased significantly at the 1-hr time and remained depressed. In view of these drastic responses, it is felt that careful consideration must be given to the choice of agent, if an anesthetic is to be employed in cardiovascular experimentation. Even more preferable would be the use of unanesthetized animals.

Submitted on June 19, 1968
Accepted on September 10, 1968




This article has been cited by other articles:


Home page
CirculationHome page
D. P. Rath, C. M. Little, H. Zhang, Z. Jiang, A. M. Abduljalil, H. Zhu, X. Tong, C. Brown, R. L. Hamlin, and P.-M. L. Robitaille
Sodium Pentobarbital Versus {alpha}-Chloralose Anesthesia : Experimental Production of Substantially Different Slopes in the Transmural CP/ATP Ratios Within the Left Ventricle of the Canine Myocardium
Circulation, January 15, 1995; 91(2): 471 - 475.
[Abstract] [Full Text]




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

Copyright © 1969 by the American Society for Pharmacology and Experimental Therapeutics.