Mild foot electrical stimulation is comparable with phenytoin in inhibiting pentylenetetrazol-induced kindling in rats

Increasing evidence demonstrates that electric stimulation has anticonvulsant effects. The present study was undertaken to investigate the effects of mild foot electrical stimulation (MFES) on the development of pentylenetetrazol (PTZ) kindling and compare its effectiveness with the more commonly us...

Full description

Saved in:
Bibliographic Details
Published inThe journal of physiological sciences Vol. 69; no. 6; pp. 1071 - 1076
Main Authors Ghasemi-Dehno, Arefe, Jand, Abolfazl, Abasi-Moghadam, Monir, Sadegh, Mehdi, Mousavi-Hasanzadeh, Morteza, Palizvan, Mohammad Reza
Format Journal Article
LanguageEnglish
Published Japan Springer 01.11.2019
BioMed Central
Springer Japan
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Increasing evidence demonstrates that electric stimulation has anticonvulsant effects. The present study was undertaken to investigate the effects of mild foot electrical stimulation (MFES) on the development of pentylenetetrazol (PTZ) kindling and compare its effectiveness with the more commonly used treatment, phenytoin. Kindling was induced in rats by repeated injections (every 24 h) of PTZ (37.5 mg/kg). The rats were subjected to either MFES (0.2 mA in intensity for a 160 ms duration with a 160 ms interval for 20 min) or phenytoin (30 mg/kg) before PTZ injections. Following this treatment, rats received MFES every other day for 10 days or 26 days after establishment of PTZ kindling. The data showed that MFES significantly inhibited development of chemical kindling induced by PTZ in rats (p = 0.001, as compared to PTZ-treated animals). This inhibitory effect is comparable with the effect of 30 mg/kg doses of phenytoin (P = 0.99, as compared to phenytoin group). However, 10 days or 26 days durations of MFES had no effect on established kindled seizures (P = 0.58 as compared to PTZ-treated animals). Our data demonstrate that although MFES significantly inhibited the development of chemical kindling, this experimental paradigm had no effect on established kindled seizures.
ISSN:1880-6546
1880-6562
DOI:10.1007/s12576-019-00726-0