Author/Authors :
Ghasemi, Fatemeh Department of Physiology - Medical School - Shahid Beheshti University of Medical Sciences, Evin, Tehran, Iran , Tamadon, Hanieh Neuroscience Research Center - Department of Physiology - Medical School - Shahid Beheshti University of Medical Sciences, Evin, Tehran, Iran , Hosseinmardi, Narges Department of Physiology - Medical School - Shahid Beheshti University of Medical Sciences, Evin, Tehran, Iran , Janahmadi, Mahyar Department of Physiology - Medical School - Shahid Beheshti University of Medical Sciences, Evin, Tehran, Iran
Abstract :
Epilepsy is a chronic neurological disease which disrupts the neuronal electrical activity.
One-third of patients are resistant to treatment with available antiepileptic agents. The use of
herbal medicine for treating several diseases including epilepsy is on the rise. Therefore, further
investigation is required to verify the safety and effectiveness of Phytomedicine in treating
diseases. The current study is an attempt to elucidate the electrophysiological mechanism of
the effect of Dorema ammoniacum gum on a cellular model of epilepsy, using intracellular
recording method. The gum was applied either after or before pentylenetetrazole, as an epileptic
drug, in order to explore the possible therapeutic and preventive effects of gum. Treatment with
D. ammoniacum gum alone increased the neuronal excitability and when applied before or
after treatment with PTZ not only did not prevent or change the electrophysiological changes
induced by PTZ but also re-enhanced the induction of hyperexcitability and epileptiform activity
through depolarizing membrane potential, increasing the firing frequency and decreasing the
AHP amplitude. However, phenobarbital, as a standard anti-epileptic agent, almost reversed the
effect of PTZ and preserved the normal firing properties of F1 neurons.
The possible candidate mechanism of the effect of gum on neuronal excitability could be
suppressive effects of gum on voltage and/or Ca2+ dependent K+ channels currents underlying
AHP.
Keywords :
Neuronal excitability , Intracellular recording , Dorema ammoniacum , Pentylenetetrazole , Epileptic activity