Behavioural effects of anatoxin, a potent nicotinic agonist, in rats

Neuropharmacology. 1992 Mar;31(3):311-4. doi: 10.1016/0028-3908(92)90182-o.

Abstract

Preliminary behavioural studies with the nicotinic agonist (+)-anatoxin have been carried with procedures sensitive to (-)-nicotine. In experimentally naive rats, (+)-anatoxin decreased locomotor activity; this effect resembled that of (-)-nicotine, but it was not blocked by mecamylamine. In nicotine-tolerant rats, (+)-anatoxin differed from (-)-nicotine because it did not increase locomotion. However, in rats trained to discriminate nicotine from saline in an operant conditioning procedure, (+)-anatoxin produced a partial nicotine-like discriminative stimulus effect that was blocked by mecamylamine, and a decreased rate of responding that was insensitive to mecamylamine. The behavioural profile of (+)-anatoxin differs from that of (-)-nicotine and it can be used for further investigations of CNS nicotinic receptors.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Toxins / pharmacology*
  • Behavior, Animal / drug effects*
  • Cyanobacteria Toxins
  • Discrimination, Psychological / drug effects
  • Ganglionic Stimulants / pharmacology*
  • Male
  • Marine Toxins / pharmacology*
  • Mecamylamine / pharmacology
  • Microcystins
  • Motor Activity / drug effects
  • Nicotine / pharmacology
  • Rats
  • Tropanes

Substances

  • Bacterial Toxins
  • Cyanobacteria Toxins
  • Ganglionic Stimulants
  • Marine Toxins
  • Microcystins
  • Tropanes
  • Mecamylamine
  • Nicotine
  • anatoxin a