Gastrodin Reduces the Severity of Status Epilepticus in the Rat Pilocarpine Model of Temporal Lobe Epilepsy by Inhibiting Nav1.6 Sodium Currents

Neurochem Res. 2017 Feb;42(2):360-374. doi: 10.1007/s11064-016-2079-6. Epub 2016 Oct 14.


Temporal lobe epilepsy (TLE) is one of the most refractory types of adult epilepsy, and treatment options remain unsatisfactory. Gastrodin (GAS), a phenolic glucoside used in Chinese herbal medicine and derived from Gastrodia elata Blume, has been shown to have remarkable anticonvulsant effects on various models of epilepsy in vivo. However, the mechanisms of GAS as an anticonvulsant drug remain to be established. By utilizing a combination of behavioral surveys, immunofluorescence and electrophysiological recordings, the present study characterized the anticonvulsant effect of GAS in a pilocarpine-induced status epilepticus (SE) rat model of TLE and explored the underlying cellular mechanisms. We found that GAS pretreatment effectively reduced the severity of SE in the acute phase of TLE. Moreover, GAS protected medial entorhinal cortex (mEC) layer III neurons from neuronal death and terminated the SE-induced bursting discharge of mEC layer II neurons from SE-experienced rats. Furthermore, the current study revealed that GAS prevented the pilocarpine-induced enhancement of Nav1.6 currents (persistent (INaP) and resurgent (INaR) currents), which were reported to play a critical role in the generation of bursting spikes. Consistent with this result, GAS treatment reversed the expression of Nav1.6 protein in SE-experienced EC neurons. These results suggest that the inhibition of Nav1.6 sodium currents may be the underlying mechanism of GAS's anticonvulsant properties.

Keywords: Entorhinal cortex; Gastrodin; Nav1.6 currents; Temporal lobe epilepsy.

MeSH terms

  • Animals
  • Benzyl Alcohols / pharmacology
  • Benzyl Alcohols / therapeutic use*
  • Disease Models, Animal
  • Dose-Response Relationship, Drug
  • Epilepsy, Temporal Lobe / drug therapy*
  • Epilepsy, Temporal Lobe / physiopathology
  • Glucosides / pharmacology
  • Glucosides / therapeutic use*
  • Male
  • NAV1.6 Voltage-Gated Sodium Channel / physiology*
  • Pilocarpine / toxicity*
  • Rats
  • Rats, Sprague-Dawley
  • Severity of Illness Index
  • Sodium Channel Blockers / pharmacology
  • Sodium Channel Blockers / therapeutic use*
  • Status Epilepticus / chemically induced
  • Status Epilepticus / drug therapy*
  • Status Epilepticus / physiopathology


  • Benzyl Alcohols
  • Glucosides
  • NAV1.6 Voltage-Gated Sodium Channel
  • Scn8a protein, rat
  • Sodium Channel Blockers
  • Pilocarpine
  • gastrodin