Clocinnamox antagonism of opioid suppression of schedule-controlled responding in rhesus monkeys

Author:

Butelman E. R.,Negus S. S.,Woods J. H.,Lewis J. W.

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology

Reference15 articles.

1. Adams JU, Paronis CA, Holtzman SG (1990) Assessment of relative intrinsic activity of mu-opioid analgesics in vivo by using beta-funaltrexamine. J Pharmacol Exp Ther 255:1027–1032

2. Burke T, Woods JH, Lewis JW, Medzihradsky F (1994) Irreversible opioid anatagonist effects of clocinnamox on opioid analgesia and mu receptor binding in mice. J Pharmacol Exp Ther 271:715–721

3. Butelman ER, France CP, Woods JH (1995a) Agonist and antagonist effects of dynorphin A-(1–13) in a thermal antinociception assay in rhesus monkeys. J Pharmacol Exp Ther 275:374–380

4. Butelman ER, Negus SS, Gatch MB, Chang KJ, Woods JH (1995b) BW373U86, a ∂-opioid receptor agonist, reverses bradykinin-induced thermal allodynia in rhesus monkeys. Eur J Pharmacol 277:285–287

5. Comer SD, Burke TF, Lewis JW, Woods JH (1992) Clocinnamox: a novel, systematically-active irreversible opioid antagonist. J Pharmacol Exp Ther 262:1051–1056

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