Anticonvulsant and Sedative Effects of Eudesmin isolated from Acorus tatarinowii on mice and rats

Phytother Res. 2015 Jul;29(7):996-1003. doi: 10.1002/ptr.5337. Epub 2015 Apr 7.

Abstract

This paper was designed to investigate anticonvulsant and sedative effects of eudesmin isolated from Acorus tatarinowii. The eudesmin (5, 10, and 20 mg/kg) was administered intraperitoneally (i.p.). The maximal electroshock test (MES) and pentylenetertrazole (PTZ)-induced seizures in male mice were used to evaluate anticonvulsant activities of eudesmin, and sedative effects of eudesmin were evaluated by pentobarbital sodium-induced sleeping time (PST) and locomotor activity in mice. Finally, the mechanisms of eudesmin were investigated by determining contents of glutamic acid (Glu) and gamma-aminobutyric acid (GABA) in epileptic mice, and expressions of glutamate decarboxylase 65 (GAD65), GABAA , Bcl-2, and caspase-3 in the brain of chronic epileptic rats. Results of MES and PTZ tests revealed that eudesmin possesses significant anticonvulsant effects, and the PST and locomotor activity tests demonstrated that eudesmin has significant sedative effects. Furthermore, our study revealed that after treatment with eudesmin, GABA contents increased, whereas Glu contents decreased, and ratio of Glu/GABA decreased. Our results also indicated that expressions of GAD65, GABAA, and Bcl-2 were up-regulated by treating with eudesmin, whereas the caspase-3 obviously was down-regulated. In conclusion, eudesmin has significant anticonvulsant and sedative effects, and the mechanism of eudesmin may be related to up-regulation of GABAA and GAD65 expressions, and anti-apoptosis of neuron the in brain.

Keywords: Acorus tatarinowii; anticonvulsant; antiepileptic; epilepsy; eudesmin; sedative.

MeSH terms

  • Acorus / chemistry*
  • Animals
  • Anticonvulsants / pharmacology*
  • Brain / drug effects
  • Brain / metabolism
  • Caspase 3 / metabolism
  • Disease Models, Animal
  • Electroshock
  • Epilepsy / drug therapy
  • Furans / pharmacology*
  • Glutamate Decarboxylase / metabolism
  • Glutamic Acid / chemistry
  • Hypnotics and Sedatives / pharmacology*
  • Lignans / pharmacology*
  • Male
  • Mice
  • Mice, Inbred ICR
  • Motor Activity / drug effects
  • Pentobarbital
  • Plant Extracts / pharmacology
  • Proto-Oncogene Proteins c-bcl-2 / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, GABA-A / metabolism
  • Seizures / chemically induced
  • Seizures / drug therapy*
  • gamma-Aminobutyric Acid / chemistry

Substances

  • Anticonvulsants
  • Furans
  • Hypnotics and Sedatives
  • Lignans
  • Plant Extracts
  • Proto-Oncogene Proteins c-bcl-2
  • Receptors, GABA-A
  • Glutamic Acid
  • eudesmin
  • gamma-Aminobutyric Acid
  • Casp3 protein, rat
  • Caspase 3
  • Glutamate Decarboxylase
  • Pentobarbital