Analgesic effects of Sazetidine-A, a new nicotinic cholinergic drug

Giovanni Cucchiaro*, Yingxian Xiao, Alfredo Gonzalez Sulser, Kenneth J. Kellar

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Background: The use of nicotinic agonists for analgesia is limited by their unacceptable side effects. Sazetidine-A is a new partial agonist nicotinic ligand that has very high selectivity for beta 2-containing nicotinic acetylcholine receptors. It potently and selectively desensitizes alpha 4 beta 2 nicotinic acetylcholine receptors without measurable effects on alpha 3 beta 4 receptors. The authors investigated the analgesic effects of Sazetidine-A using the formalin model of chronic inflammatory pain.

Methods: The formalin test was conducted after rats received intraperitoneal saline, Sazetidine-A (0.125, 0.25, 0.5, 1, 2 mg/kg), or subcutaneous epibatidine (2.5-5-10 mu g/kg). In other experiments, Sazetidine-A was preceded by naloxone (0.5 mg/kg) or mecamylamine (10 mg). Effects of Sazetidine-A and epibatidine on locomotor were tested in an open field, and seizure activity was measured using the Racine scale. Locus coeruleus neuron extracellular single-unit spontaneous discharge was recorded in anesthetized animals after Sazetidine-A and epibatidine.

Results: Higher doses of Sazetidine-A (0-5, 1, or 2 mg/kg) induced analgesia, with pain scores significantly lower than those seen after saline, lower doses of Sazetidine-A, and epibatidine (P <0.001). Naloxone did not antagonize the effects of Sazetidine-A, and mecamylamine had partial, dose-dependent antagonistic effects. Epibatidine excited locus coeruleus neurons, whereas Sazetidine-A had no effect on these neurons. Epibatidine and Sazetidine-A affected animals' locomotor activity for the initial 20 min. While analgesic doses of epibatidine caused seizures, no seizure activity or other neurologic complications were seen in animals that received as much as four times the minimum analgesic dose of Sazetidine-A.

Conclusions: Sazetidine-A seems to be a potent analgesic without causing neurologic side effects.

Original languageEnglish
Pages (from-to)512-519
Number of pages8
Issue number3
Publication statusPublished - Sept 2008

Keywords / Materials (for Non-textual outputs)

  • MICE


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