Skip to main content
Advertisement

Main menu

  • Home
  • Articles
    • Current Issue
    • Fast Forward
    • Latest Articles
    • Special Sections
    • Archive
  • Information
    • Instructions to Authors
    • Submit a Manuscript
    • FAQs
    • For Subscribers
    • Terms & Conditions of Use
    • Permissions
  • Editorial Board
  • Alerts
    • Alerts
    • RSS Feeds
  • Virtual Issues
  • Feedback
  • Submit
  • Other Publications
    • Drug Metabolism and Disposition
    • Journal of Pharmacology and Experimental Therapeutics
    • Molecular Pharmacology
    • Pharmacological Reviews
    • Pharmacology Research & Perspectives
    • ASPET

User menu

  • My alerts
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Pharmacology and Experimental Therapeutics
  • Other Publications
    • Drug Metabolism and Disposition
    • Journal of Pharmacology and Experimental Therapeutics
    • Molecular Pharmacology
    • Pharmacological Reviews
    • Pharmacology Research & Perspectives
    • ASPET
  • My alerts
  • Log in
  • My Cart
Journal of Pharmacology and Experimental Therapeutics

Advanced Search

  • Home
  • Articles
    • Current Issue
    • Fast Forward
    • Latest Articles
    • Special Sections
    • Archive
  • Information
    • Instructions to Authors
    • Submit a Manuscript
    • FAQs
    • For Subscribers
    • Terms & Conditions of Use
    • Permissions
  • Editorial Board
  • Alerts
    • Alerts
    • RSS Feeds
  • Virtual Issues
  • Feedback
  • Submit
  • Visit jpet on Facebook
  • Follow jpet on Twitter
  • Follow jpet on LinkedIn
Research ArticleArticle

ELECTROLYTE CONTENT OF PERFUSED RAT VENTRICLES EXPOSED TO HALOTHANE OR ANOXIA

Raymond R. Paradise and Lionell K. Griffith
Journal of Pharmacology and Experimental Therapeutics November 1966, 154 (2) 281-288;
Raymond R. Paradise
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Lionell K. Griffith
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Info & Metrics
  • eLetters
  • PDF
Loading

Abstract

A reproducible method has been devised for depressing the force of contraction of isolated perfused rat hearts with halothane. Approximately 6 mg/100 ml of halothane in the perfusate were required to maintaiui 50% depression over a 2-hr period. To achieve 98% depression, 17 mg/100 ml were required. Recovery of force of contraction was virtually complete on stopping the administration of halothane. Neither concentration of halothane resulted in a significant change in perfusion rate, but the latter concentration produced a decrease in tissue potassium content. Anoxia (i.e., 95% N2-5% CO2 imistead of 95% 02-5% CO2) produced a 90% decrease in force of contraction, which was maintained over a 2-hr period. Recovery of force of contraction upon admission of oxygen was slower and less complete than recovery from halothane. In addition, anoxia produced an increase in perfusion rate and a decrease in tissue potassium content. Despite the fact that anoxia and halothane produced similar changes in force of contraction and potassium content, the differences in perfusion rate and recovery of force of contraction indicate that different biochemical changes are occurring in the cells.

Footnotes

    • Received March 9, 1966.
    • Accepted May 26, 1966.
  • © 1966 by The Williams & Wilkins Company

JPET articles become freely available 12 months after publication, and remain freely available for 5 years. 

Non-open access articles that fall outside this five year window are available only to institutional subscribers and current ASPET members, or through the article purchase feature at the bottom of the page. 

 

  • Click here for information on institutional subscriptions.
  • Click here for information on individual ASPET membership.

 

Log in using your username and password

Forgot your user name or password?

Purchase access

You may purchase access to this article. This will require you to create an account if you don't already have one.
PreviousNext
Back to top

In this issue

Journal of Pharmacology and Experimental Therapeutics
Vol. 154, Issue 2
1 Nov 1966
  • Table of Contents
  • Table of Contents (PDF)
  • Index by author
  • Editorial Board (PDF)
  • Front Matter (PDF)
Download PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Journal of Pharmacology and Experimental Therapeutics article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
ELECTROLYTE CONTENT OF PERFUSED RAT VENTRICLES EXPOSED TO HALOTHANE OR ANOXIA
(Your Name) has forwarded a page to you from Journal of Pharmacology and Experimental Therapeutics
(Your Name) thought you would be interested in this article in Journal of Pharmacology and Experimental Therapeutics.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Research ArticleArticle

ELECTROLYTE CONTENT OF PERFUSED RAT VENTRICLES EXPOSED TO HALOTHANE OR ANOXIA

Raymond R. Paradise and Lionell K. Griffith
Journal of Pharmacology and Experimental Therapeutics November 1, 1966, 154 (2) 281-288;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero

Share
Research ArticleArticle

ELECTROLYTE CONTENT OF PERFUSED RAT VENTRICLES EXPOSED TO HALOTHANE OR ANOXIA

Raymond R. Paradise and Lionell K. Griffith
Journal of Pharmacology and Experimental Therapeutics November 1, 1966, 154 (2) 281-288;
Reddit logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
  • Info & Metrics
  • eLetters
  • PDF

Related Articles

Cited By...

More in this TOC Section

  • PST3093 Stimulates SERCA2a and Improves Cardiac Function
  • CRV431 Decreases Liver Fibrosis and Tumor Development
  • Pharmacological Characterization of Nicotine-Induced Seizures in Mice
Show more Article

Similar Articles

Advertisement
  • Home
  • Alerts
Facebook   Twitter   LinkedIn   RSS

Navigate

  • Current Issue
  • Fast Forward by date
  • Fast Forward by section
  • Latest Articles
  • Archive
  • Search for Articles
  • Feedback
  • ASPET

More Information

  • About JPET
  • Editorial Board
  • Instructions to Authors
  • Submit a Manuscript
  • Customized Alerts
  • RSS Feeds
  • Subscriptions
  • Permissions
  • Terms & Conditions of Use

ASPET's Other Journals

  • Drug Metabolism and Disposition
  • Molecular Pharmacology
  • Pharmacological Reviews
  • Pharmacology Research & Perspectives
ISSN 1521-0103 (Online)

Copyright © 2023 by the American Society for Pharmacology and Experimental Therapeutics