HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Antinociceptive and anti-inflammatory properties of an adenosine kinase inhibitor and an adenosine deaminase inhibitor.

Abstract
Spinal administration of an adenosine kinase inhibitor, alone or in combination with an adenosine deaminase inhibitor, produces antinociception in inflammatory pain tests. In the present study, we examined the antinociceptive and anti-inflammatory effects produced by the peripheral (intraplantar) administration of 5'-amino-5'-deoxyadenosine (an adenosine kinase inhibitor), 2'-deoxycoformycin (an adenosine deaminase inhibitor), and combinations of both agents in the carrageenan-induced thermal hyperalgesia and paw oedema model in the rat. When injected in the ipsilateral paw immediately prior to carrageenan injection, both agents produced antinociception only at the highest dose (1 micromol), whereas a reduction in paw swelling was evident at a lower dose (300 nmol). Significant augmentation in both the antinociceptive and anti-inflammatory effects was seen when 5'-amino-5'-deoxyadenosine and 2'-deoxycoformycin were co-administered in equimolar doses at all dose levels. Both effects were mediated via activation of adenosine receptors, as indicated by blockade by an adenosine receptor antagonist. When administered into the contralateral paw, 1 micromol 5'-amino-5'-deoxyadenosine+1 micromol 2'-deoxycoformycin produced prominent antinociception, indicating a systemic drug activity. There was only a modest reduction in paw oedema in the carrageenan-injected (ipsilateral) paw, suggesting that much of this activity was locally mediated. Reversal of systemic effects on thermal thresholds by an intrathecal adenosine receptor antagonist implicates a spinal site of action in this instance. An ipsilateral administration of 1 micromol 5'-amino-5'-deoxyadenosine, but not 1 micromol 2'-deoxycoformycin, reduced carrageenan-induced c-Fos expression in the spinal dorsal horn, and this was further reduced by the peripheral co-injection of the two agents. These results provide evidence for a predominantly spinal antinociceptive effect and a predominantly peripheral anti-inflammatory effect produced by inhibitors of adenosine kinase and adenosine deaminase.
AuthorsA Poon, J Sawynok
JournalEuropean journal of pharmacology (Eur J Pharmacol) Vol. 384 Issue 2-3 Pg. 123-38 (Nov 19 1999) ISSN: 0014-2999 [Print] Netherlands
PMID10611432 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Adenosine Deaminase Inhibitors
  • Analgesics
  • Anti-Inflammatory Agents
  • Central Nervous System Stimulants
  • Deoxyadenosines
  • Enzyme Inhibitors
  • Proto-Oncogene Proteins c-fos
  • Purinergic P1 Receptor Antagonists
  • 5'-amino-5'-deoxyadenosine
  • Pentostatin
  • Caffeine
  • 3,7-dimethyl-1-propargylxanthine
  • Carrageenan
  • Adenosine Kinase
  • Adenosine Deaminase
  • Theobromine
Topics
  • Adenosine Deaminase (metabolism)
  • Adenosine Deaminase Inhibitors
  • Adenosine Kinase (antagonists & inhibitors, metabolism)
  • Analgesics (pharmacology)
  • Animals
  • Anti-Inflammatory Agents (pharmacology)
  • Caffeine (pharmacology)
  • Carrageenan (adverse effects)
  • Central Nervous System Stimulants (pharmacology)
  • Deoxyadenosines (pharmacology)
  • Dose-Response Relationship, Drug
  • Drug Synergism
  • Edema (chemically induced, prevention & control)
  • Enzyme Inhibitors (pharmacology)
  • Hindlimb
  • Hyperalgesia (prevention & control)
  • Injections, Spinal
  • Male
  • Nociceptors (drug effects)
  • Pain (prevention & control)
  • Pentostatin (pharmacology)
  • Proto-Oncogene Proteins c-fos (drug effects, metabolism)
  • Purinergic P1 Receptor Antagonists
  • Rats
  • Rats, Sprague-Dawley
  • Spinal Cord (drug effects, metabolism)
  • Theobromine (analogs & derivatives, pharmacology)
  • Time Factors

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: