Literature DB >> 8214659

Previous administration of indomethacin or naloxone did not influence ketorolac antinociception in mice.

H F Miranda1, F Sierralta, G Pinardi.   

Abstract

We studied the effects of the inhibition of prostaglandin biosynthesis and opioid antagonism in the antinociceptive action of ketorolac using the mouse acetic acid writhing test. Ketorolac was administered via the intraperitoneal, intrathecal, or intracerebroventricular routes. Although the ketorolac induced a significant dose-dependent antinociceptive effect, the intracerebroventricular administration was the most effective route. Indomethacin and naloxone pretreatments did not change the ketorolac-induced antinociception. The present findings suggest that this antinociceptive action of ketorolac is not mediated by the inhibition of prostaglandin biosynthesis nor by activation of opioid receptors.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8214659     DOI: 10.1213/00000539-199310000-00016

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  4 in total

Review 1.  Ketorolac. A reappraisal of its pharmacodynamic and pharmacokinetic properties and therapeutic use in pain management.

Authors:  J C Gillis; R N Brogden
Journal:  Drugs       Date:  1997-01       Impact factor: 9.546

2.  Interaction between the antinociceptive effect of ketoprofen and adrenergic modulatory systems.

Authors:  G Pinardi; F Sierralta; H F Miranda
Journal:  Inflammation       Date:  2001-08       Impact factor: 4.092

3.  Intrathecal ketorolac tromethamine produces analgesia after chronic constriction injury of sciatic nerve in rat.

Authors:  W C Parris; P K Janicki; B Johnson; J L Horn
Journal:  Can J Anaesth       Date:  1996-08       Impact factor: 5.063

4.  The analgesic interaction of tramadol and morphine in rats: An isobolographic study.

Authors:  Hesam Savadkoohi; Nasser Vesal
Journal:  Vet Res Forum       Date:  2019-03-15       Impact factor: 1.054

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.