JPET

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Journal of Pharmacology And Experimental Therapeutics Fast Forward
First published on November 16, 2005; DOI: 10.1124/jpet.105.094276


0022-3565/06/3163-1195-1201$20.00
JPET 316:1195-1201, 2006
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
jpet.105.094276v1
316/3/1195    most recent
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
Right arrow Citation Map
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 Peckham, E. M.
Right arrow Articles by Traynor, J. R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Peckham, E. M.
Right arrow Articles by Traynor, J. R.

BEHAVIORAL PHARMACOLOGY

Comparison of the Antinociceptive Response to Morphine and Morphine-Like Compounds in Male and Female Sprague-Dawley Rats

Elizabeth M. Peckham, and John R. Traynor

Department of Pharmacology, University of Michigan Medical School, Ann Arbor, Michigan

Male rats are more sensitive to the antinociceptive effects of morphine than female rats. This difference is seen across several rat strains using a variety of nociceptive stimuli. However, the literature in regard to sex differences in antinociceptive responses to µ-opioids other than morphine is less consistent. The present study was designed to examine whether there is a structure-activity rationale that determines which µ-opioids will show a differential antinociceptive response between male and female rats. A series of morphinans closely related in structure to morphine, namely, codeine, heroin, hydrocodone, hydromorphone, oxymorphone, and oxycodone, were examined for their antinociceptive activity in male and female Sprague-Dawley rats and compared with the structurally unrelated µ-opioid agonists methadone and fentanyl. Antinociception was measured by the warm-water tail-withdrawal assay. The results show that morphine is more potent in males compared with females > hydromorphone = hydrocodone = oxymorphone, but there was no observable sex difference in the antinociceptive potency of codeine, heroin, oxycodone, methadone, or fentanyl. The potency to stimulate guanosine 5'-O-(3-[35 S]thio)triphosphate ([35S]GTP{gamma}S) binding and binding affinity of the various morphinans was compared in rat glioma C6 cells expressing the rat µ-opioid receptor; relative efficacy was also compared by stimulation of [35S]GTP{gamma}S binding in slices of rat brain thalamus. The presence of a sex difference in antinociceptive responsiveness was not related to drug potency, efficacy, or affinity. Consequently, it is likely that differential metabolism of the opioid, possibly by glucuronidation, determines the presence or absence of a sex difference.


Received for publication August 16, 2005
Accepted November 10, 2005.

Address correspondence to: Dr. John R. Traynor, University of Michigan, 1150 West Medical Center Dr. 1301 MSRB III, Ann Arbor, MI 48109-0632. E-mail: jtraynor{at}umich.edu




This article has been cited by other articles:


Home page
Anesth. Analg.Home page
H. Lenz, L. Sandvik, E. Qvigstad, C. E. Bjerkelund, and J. Raeder
A Comparison of Intravenous Oxycodone and Intravenous Morphine in Patient-Controlled Postoperative Analgesia After Laparoscopic Hysterectomy
Anesth. Analg., October 1, 2009; 109(4): 1279 - 1283.
[Abstract] [Full Text] [PDF]


Home page
Mol. Pharmacol.Home page
M. S. Virk and J. T. Williams
Agonist-Specific Regulation of {micro}-Opioid Receptor Desensitization and Recovery from Desensitization
Mol. Pharmacol., April 1, 2008; 73(4): 1301 - 1308.
[Abstract] [Full Text] [PDF]


Home page
J. Pharmacol. Exp. Ther.Home page
D. S. Gupta, H. von Gizycki, and A. R. Gintzler
Sex-/Ovarian Steroid-Dependent Release of Endomorphin 2 from Spinal Cord
J. Pharmacol. Exp. Ther., May 1, 2007; 321(2): 635 - 641.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
D. L. Shuey, C. Woodland, C. Tremblay, R. Gregson, and R. J. Gerson
Oxymorphone Hydrochloride, a Potent Opioid Analgesic, Is Not Carcinogenic in Rats or Mice
Toxicol. Sci., March 1, 2007; 96(1): 162 - 173.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
J. Claiborne, S. Nag, and S. S. Mokha
Activation of Opioid Receptor Like-1 Receptor in the Spinal Cord Produces Sex-Specific Antinociception in the Rat: Estrogen Attenuates Antinociception in the Female, whereas Testosterone Is Required for the Expression of Antinociception in the Male
J. Neurosci., December 13, 2006; 26(50): 13048 - 13053.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
E. Bostrom, U. S. H. Simonsson, and M. Hammarlund-Udenaes
In Vivo Blood-Brain Barrier Transport of Oxycodone in the Rat: Indications for Active Influx and Implications for Pharmacokinetics/Pharmacodynamics
Drug Metab. Dispos., September 1, 2006; 34(9): 1624 - 1631.
[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 © 2006 by the American Society for Pharmacology and Experimental Therapeutics.