Positive allosteric modulators of alpha 7 nicotinic acetylcholine receptors enhance procognitive effects of conventional anti-Alzheimer drugs in scopolamine-treated rats

Behav Brain Res. 2020 May 15:385:112547. doi: 10.1016/j.bbr.2020.112547. Epub 2020 Feb 19.

Abstract

Positive allosteric modulators (PAMs) of alpha 7 nicotinic acetylcholine receptors (α7-nAChRs) may represent a novel approach to attenuate cognitive decline in Alzheimer's disease (AD). One possible scenario for the use of this class of compounds is their combination with currently approved anti-AD drugs. We thus evaluated the efficacy of co-administration of inactive doses of type I and type II α7-nAChR PAMs (CCMI and PNU-120596, respectively) with acetylcholinesterase inhibitors (AChEIs), donepezil and galantamine, or with a non-competitive glutamate N-methyl-D-aspartate receptor antagonist, memantine, in ameliorating scopolamine-induced memory deficits in the novel object recognition test in rats. Both CCMI and PNU-120596 as well as donepezil, galantamine and memantine attenuated the scopolamine-induced recognition impairments. Interestingly, the combined administration of previously established sub-effective doses of the tested PAMs (0.1 mg/kg) with either AChEIs, donepezil (0.3 mg/kg) and galantamine (0.1 mg/kg), or memantine (0.3 mg/kg) also restored object recognition memory in scopolamine-treated animals. These findings suggest the therapeutic potential of α7-nAChR PAMs as an augmentation strategy for cognitive enhancement in AD.

Keywords: Acetylcholinesterase inhibitors; Allosteric modulators; Alpha 7 nicotinic acetylcholine receptors; Alzheimer’s disease; Memantine.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Allosteric Regulation
  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / physiopathology
  • Animals
  • Cholinergic Antagonists / toxicity
  • Cholinesterase Inhibitors / pharmacology*
  • Disease Models, Animal
  • Donepezil / pharmacology
  • Drug Synergism
  • Excitatory Amino Acid Antagonists / pharmacology*
  • Galantamine / pharmacology
  • Isoxazoles / pharmacology*
  • Memantine / pharmacology
  • Nootropic Agents / pharmacology
  • Phenylurea Compounds / pharmacology*
  • Rats
  • Recognition, Psychology / drug effects*
  • Scopolamine / toxicity
  • alpha7 Nicotinic Acetylcholine Receptor / agonists*

Substances

  • (N-(4-chlorophenyl))-alpha-((4-chlorophenyl)-aminomethylene)-3-methyl-5-isoxazoleacet-amide
  • 1-(5-chloro-2,4-dimethoxyphenyl)-3-(5-methylisoxazol-3-yl)urea
  • Cholinergic Antagonists
  • Cholinesterase Inhibitors
  • Chrna7 protein, rat
  • Excitatory Amino Acid Antagonists
  • Isoxazoles
  • Nootropic Agents
  • Phenylurea Compounds
  • alpha7 Nicotinic Acetylcholine Receptor
  • Galantamine
  • Donepezil
  • Scopolamine
  • Memantine