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 (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Conklin, D. R.
Right arrow Articles by Eisenach, J. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Conklin, D. R.
Right arrow Articles by Eisenach, J. C.
Related Collections
Right arrow Pain
Right arrow Pharmacology

Anesth Analg 2003;96:191-194
© 2003 International Anesthesia Research Society


PAIN MEDICINE

Intrathecal Ketorolac Enhances Antinociception from Clonidine

Dawn R. Conklin, BA, and James C. Eisenach, MD

From the Department of Anesthesiology and Center for the Study of Pharmacologic Plasticity in the Presence of Pain, Wake Forest University School of Medicine, Winston-Salem, North Carolina

Address correspondence and reprint requests to James C. Eisenach, MD, Department of Anesthesiology, Wake Forest University School of Medicine, Medical Center Blvd., Winston-Salem, NC 27157–1009. Address e-mail to eisenach{at}wfubmc.edu

Although both {alpha}2-adrenergic agonists and cyclooxygenase inhibitors produce analgesia, their exact sites of action and interaction remain unclear. A previous report demonstrated a surprising inhibition of antinociception in rats from intrathecal clonidine by co-administered ketorolac. There are no other reports of interaction between these two classes of analgesics. We therefore reexamined this interaction, determining the effect of intrathecal clonidine and ketorolac alone and in combination in normal rats. Clonidine, but not ketorolac, produced antinociception to noxious hind paw thermal stimulation. The addition of ketorolac significantly enhanced the effect of clonidine, indicating a synergistic interaction for analgesia. Although the reasons for the discrepancy between this and the previous report are unclear, these results are consistent with previous studies that indicate an antinociceptive action of intrathecal {alpha}2-adrenergic agonists in the normal condition, a lack of such effect for cyclooxygenase inhibitors, and positive reinforcing effects of these two systems when co-stimulated.

IMPLICATIONS: Spinal injection of the {alpha}2-adrenergic agonist clonidine and the cyclooxygenase inhibitor ketorolac results in a synergistic interaction for antinociception in normal animals, suggesting that the combination of these drugs will enhance rather than detract from the analgesia of either alone.




This article has been cited by other articles:


Home page
Anesth. Analg.Home page
J. P. Rathmell, T. R. Lair, and B. Nauman
The Role of Intrathecal Drugs in the Treatment of Acute Pain
Anesth. Analg., November 1, 2005; 101(5S_Suppl): S30 - 43.
[Abstract] [Full Text] [PDF]


Home page
Anesth. Analg.Home page
Y.-C. Hsieh, W.-Y. Liang, S.-K. Tsai, and C.-S. Wong
Intrathecal Ketorolac Pretreatment Reduced Spinal Cord Ischemic Injury in Rats
Anesth. Analg., April 1, 2005; 100(4): 1134 - 1139.
[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 © 2003 by the International Anesthesia Research Society.