The neuroprotective effect of electrical stimulation in chronic epilepsy
10.3760/cma.j.issn.0254-1424.2014.04.003
- VernacularTitle:三叉神经电刺激对慢性癫痫大鼠癫痫状态所致海马神经元损伤的保护作用观察
- Author:
Jian ZUO
;
Huiyan HE
;
Qianqian WANG
;
Na YIN
;
Chengjuan XIE
;
Yu WANG
- Publication Type:Journal Article
- Keywords:
Epilepsy;
Transcutaneous electrical stimulation;
Trigeminal nerve;
Neuroprotection;
Glutamic acid decarboxylase 65/67
- From:Chinese Journal of Physical Medicine and Rehabilitation
2014;36(4):250-254
- CountryChina
- Language:Chinese
-
Abstract:
Objective To study any protection against hippocampal neuron damage induced by epilepsy (SE) provided by transcutaneous stimulation (TNS) of the trigeminal nerve and to document any effect of such stimulation on the expression of glutamic acid decarboxylase (GAD) 65/67.Methods Pilocarpine injection was used to induce epilepsy in healthy male Sprague-Dawley rats which were then randomly divided into a treatment group and a model group.Rats which had not received the pilocarpine injection served as normal controls.In the treatment group the rats were given electrostimulation for one month after the first spontaneous seizure following the injection of pilocarpine.In the model group they were given sham TNS for one month.After the month of stimula-tion,immunohistochemistry was used to detect the expression of GAD65/67 in the hippocampus.Terminal deoxy-nucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) assays and Nissl staining were applied to deter-mine apoptosis and neuron loss in the hippocampus.Results Significantly less apoptosis was observed in the treatment group than in model group at 24 h,48 h and 72 h post-injection.Compared to the model group,average GAD65/67 expression had increased significantly in the treatment group at 24 h,72 h,1 week,2 weeks and 4 weeks post-stimulation.GAD65 expression reached its peak from 72 h to 1 week post-stimulation,then decreased to the level of the control group by 4 weeks post-stimulation.The expression of GAD67 remained elevated at all the time points employed.Conclusions TNS can significantly protect hippocampal neurons from damage in epilepsy,at least in rats.The underlying anti-epileptic and neuroprotective mechanisms may involve increased inhibitory transmission induced by the stimulation.
