Effect of rutin on anxiety-like behavior and activity of acetylcholinesterase isoforms in specific brain regions of pentylenetetrazol-treated mice

Epilepsy Behav. 2020 Jan:102:106632. doi: 10.1016/j.yebeh.2019.106632. Epub 2019 Nov 17.

Abstract

The aim of the present study was to investigate the effect of rutin administration (100 mg/kg/day) to pentylenetetrazol (PTZ)-treated Balb-c mice (60 mg/kg/day), with respect to anxiety-like behavior using both open-field and elevated plus-maze (EPM) tests, and acetylcholinesterase (AChE) activity in salt-soluble (SS) fraction and detergent-soluble (DS) fraction of the cerebral cortex, hippocampus, striatum, midbrain, and diencephalon. Our results demonstrated that the administration of PTZ in 3 doses and the induction of seizures increased significantly anxiety behavior of mice and reduced significantly DS-AChE activity in all brain regions examined, while the reduction in the SS fraction was brain region-specific. Rutin administration to normal mice did not affect their behavior, while it induced a brain region-specific reduction in SS-AChE and a significant decrease in DS-AChE in all brain regions. We demonstrated for the first time that pretreatment of PTZ-mice with rutin (PTZ + Rutin group) prevented the manifestation of anxiety and induced interestingly a further significant reduction on the SS- and DS-AChE activities only in the cerebral cortex and striatum, in comparison with PTZ group. Our results show that rutin exhibits an important anxiolytic effect and an anticholinesterase activity in specific brain areas in the seizure model of PTZ.

Keywords: Acetylcholinesterase isoforms activity; Anxiety-like behavior; Brain regions; Pentylenetetrazol; Rutin; Seizure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Anxiety / drug therapy*
  • Anxiety / enzymology*
  • Brain / drug effects
  • Brain / enzymology*
  • Isoenzymes / metabolism
  • Male
  • Maze Learning / drug effects
  • Maze Learning / physiology
  • Mice
  • Mice, Inbred BALB C
  • Pentylenetetrazole / toxicity*
  • Rutin / pharmacology
  • Rutin / therapeutic use*
  • Seizures / chemically induced
  • Seizures / drug therapy*
  • Seizures / enzymology*
  • Treatment Outcome

Substances

  • Isoenzymes
  • Rutin
  • Acetylcholinesterase
  • Pentylenetetrazole