Morphine and ABT-594 (a Nicotinic Acetylcholine Agonist) Exert Centrally Mediated Antinociception in the Rat Cyclophosphamide Cystitis Model of Visceral Pain

Author:

Joshi S.K.,Mikusa Joe P.,Weaver Brenda,Honore Prisca

Publisher

Elsevier BV

Subject

Anesthesiology and Pain Medicine,Neurology (clinical),Neurology

Reference52 articles.

1. Biological basis of visceral pain: Recent developments;Al-Chaer;Pain,2002

2. Peripheral and central mechanisms of visceral sensitization in man;Anand;Neurogastroenterol Motil,2007

3. ABT-594 [(R)-5-(2-azetidinylmethoxy)-2-chloropyridine]: A novel, orally effective antinociceptive agent acting via neuronal nicotinic acetylcholine receptors, II: In vivo characterization;Bannon;J Pharmacol Exp Ther,1998

4. ABT-594, a novel cholinergic channel modulator, is efficacious in nerve ligation and diabetic neuropathy models of neuropathic pain;Bannon;Brain Res,1998

5. The cyclooxygenase-2 inhibitor GW406381X [2-(4-ethoxyphenyl)-3-[4-(methylsulfonyl)phenyl]-pyrazolo[1,5-b]pyridazine] is effective in animal models of neuropathic pain and central sensitization;Bingham;J Pharmacol Exp Ther,2005

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