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Effect of selol on the opioids activity in streptozotocin induced hyperalgesia.

Abstract
We examined the effect of the opioid receptor agonists and the effect of an antioxidant selol, which is an organoselenium compound on antinociceptive action of opioid agonists in diabetic neuropathic pain model. Streptozotocin (STZ) induced hyperglycemia accompanied by a prolonged decrease in nociceptive threshold is considered a useful model of experimental hyperalgesia. The changes in pain thresholds were determined using mechanical stimuli--the modification of the classic paw withdrawal Randall-Selitto test. Neither morphine, fentanyl nor buprenorphine administered alone in 7 consecutives days modified the STZ induced hyperalgesia, whereas selol slightly increased the nociceptive threshold. Pretreatment with selol markedly enhanced the analgesic activity of all three investigated opioids. Concomitant administration of selol and opioids in alleviation of neoplastic pains seems to be justified.
AuthorsMagdalena Bujalska, Renata Winecka, Stanisław W Gumułka
JournalActa poloniae pharmaceutica (Acta Pol Pharm) 2008 Nov-Dec Vol. 65 Issue 6 Pg. 691-6 ISSN: 0001-6837 [Print] Poland
PMID19172850 (Publication Type: Journal Article)
Chemical References
  • Analgesics, Opioid
  • Antioxidants
  • Selenium Compounds
  • selol
  • Buprenorphine
  • Streptozocin
  • Morphine
  • Fentanyl
Topics
  • Analgesics, Opioid (pharmacology)
  • Animals
  • Antioxidants (pharmacology)
  • Buprenorphine (pharmacology)
  • Diabetes Mellitus, Experimental (complications)
  • Diabetic Neuropathies (drug therapy, physiopathology)
  • Drug Synergism
  • Drug Therapy, Combination
  • Fentanyl (pharmacology)
  • Hyperalgesia (drug therapy, etiology)
  • Male
  • Morphine (pharmacology)
  • Pain Measurement
  • Pain Threshold (drug effects)
  • Rats
  • Rats, Wistar
  • Selenium Compounds (pharmacology)
  • Streptozocin

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