JOURNAL HOME CME HOME THIS MONTH PAST ISSUES ETOC COLLECTIONS
AUTHORS REVIEWERS EDITORIAL BOARD FEEDBACK RSS HELP
A&A International Anesthesia Research Society
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a colleague
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
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 ISI Web of Science (10)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Asai, T.
Right arrow Articles by Power, I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Asai, T.
Right arrow Articles by Power, I.
Anesth Analg 1999;88:204-208
© 1999 International Anesthesia Research Society


GENERAL ARTICLES

Naloxone Inhibits Gastric Emptying in the Rat

Takashi Asai, MD, PhD*,*, and Ian Power, BSc(Hons), MD, FRCA{dagger}

*Department of Anesthesiology, Kansai Medical University, Moriguchi City, Osaka, Japan; *Department of Anaesthetics and Intensive Care Medicine, University of Wales College of Medicine, Cardiff, United Kingdom; and {dagger}Department of Anaesthesia and Pain Management, Royal North Shore Hospital and University of Sydney, St. Leonards, New South Wales, Australia

Address correspondence and reprint requests to Takashi Asai, Department of Anesthesiology, Kansai Medical University, 10–15 Fumizono-cho, Moriguchi City, Osaka, 570-8507, Japan. Address e-mail to asait{at}takii.kmu.ac.jp

Naloxone is generally considered to be a pure antagonist, but it may produce several behavioral effects, such as hyperalgesia or stimulation of respiration. We studied the effect of naloxone on gastric emptying and gastrointestinal transit in rats. Six to eight Wistar rats (200–250 g) were used for each experiment. Either saline or naloxone (0.01–10 mg/kg) was injected intraperitoneally at 0 min. At 30 min, radiolabeled saline or milk 1 mL was infused into the stomach. At 60 min, gastric emptying and gastrointestinal transit were calculated by measuring the radioactivity in the gastrointestinal tract. Naloxone significantly inhibited gastric emptying of saline (P = 0.002) and of milk (P < 0.05), but not the gastrointestinal transit of either (P > 0.05). Gastric emptying of saline showed a significant peak (P < 0.05) in the dose-response curve at 0.7 mg/kg. Therefore, naloxone significantly inhibits gastric emptying of saline and milk, but not the gastrointestinal transit of either.

Implications: Although naloxone is generally considered to be a pure opioid receptor antagonist, it delays gastric emptying of saline or milk, as does morphine in the rat. However, it is uncertain from our results whether naloxone inhibited gastric emptying by antagonizing the effects of endogenous opioids.




This article has been cited by other articles:


Home page
JNMHome page
D. L. Anderson, F. D. Bartholomeusz, I. D. Kirkwood, B. E. Chatterton, G. Summersides, S. Penglis, T. Kuchel, and L. Sansom
Liquid Gastric Emptying in the Pig: Effect of Concentration of Inhaled Isoflurane
J. Nucl. Med., July 1, 2002; 43(7): 968 - 971.
[Abstract] [Full Text] [PDF]




Lippincott, Williams & Wilkins Anesthesia & Analgesia® is published for the International Anesthesia Research Society® by Lippincott Williams & Wilkins with the assistance of Stanford University Libraries' HighWire Press®. Copyright 2006 by the International Anesthesia Research Society. Online ISSN: 1526-7598   Print ISSN: 0003-2999 HighWire Press
Copyright © 1999 by the International Anesthesia Research Society.