Amelioration of experimental amnesia (passive avoidance failure) in rodents by the selective M1 agonist AF102B

Jpn J Pharmacol. 1988 Dec;48(4):502-6. doi: 10.1254/jjp.48.502.

Abstract

Effect of AF102B (cis-2-methylspiro-(1,3-oxathiolane-5,3')-quinuclidine) on experimental amnesia was examined using a passive avoidance task in rodents. The amnesia was produced by anti-cholinergic agents, AF64A (intracerebroventricularly) and scopolamine (subcutaneously). AF102B ameliorated the memory deficits in AF64A-treated rats at 0.1-1 mg/kg, i.p. and at 1-5 mg/kg p.o. and in scopolamine-treated mice at 1-10 mg/kg, i.p. These results suggest that AF102B may compensate for central cholinergic defects and could be developed as a possible therapeutic drug for senile dementia of the Alzheimer type.

MeSH terms

  • Amnesia / chemically induced
  • Amnesia / physiopathology*
  • Animals
  • Arecoline / pharmacology
  • Aziridines / toxicity
  • Choline / analogs & derivatives
  • Choline / toxicity
  • Male
  • Memory / drug effects*
  • Mice
  • Mice, Inbred Strains
  • Oxotremorine / pharmacology
  • Parasympathomimetics / pharmacology*
  • Quinuclidines / pharmacology*
  • Retention, Psychology / drug effects*
  • Scopolamine / toxicity
  • Thiophenes*

Substances

  • Aziridines
  • Parasympathomimetics
  • Quinuclidines
  • Thiophenes
  • Arecoline
  • Oxotremorine
  • ethylcholine aziridinium
  • Scopolamine
  • cevimeline
  • Choline