Effect of serotonin depletion on seizures learning-memory in pilocarpine-induced epileptic rats.
- Author:
Xiao-chai LV
1
;
Hua-pin HUANG
;
Wan-hui LIN
;
Sheng-gen CHEN
Author Information
- Publication Type:Journal Article
- MeSH: 5,7-Dihydroxytryptamine; toxicity; Animals; Epilepsy; chemically induced; metabolism; psychology; Male; Maze Learning; Memory; Pilocarpine; adverse effects; Raphe Nuclei; Rats; Rats, Sprague-Dawley; Serotonin; metabolism
- From: Chinese Journal of Applied Physiology 2012;28(3):210-213
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the relationship between serotonin (5-HT) and epilepsy and the mechanism of learning-memory in pilocarpine (PILO)-induced epileptic rats after 5,7-dihydroxytryptamine (5,7-DHT) microinjection in median raphe nucleus.
METHODSAdult S D rats were randomly divided into 3 groups: PILO group, PILO+ 5,7-DHT group, vehicle control group; PILO group was divided into two groups by status epilepticus (SE): PILO + SE group and PILO - SE group. The rats' seizures and cortex electroencephalography (EEG) were observed by video EEG. The rats' spatial learning-memory was evaluated by Morris water maze. Finally, serotonergic neuron in raphe nuclei was observed by immunohistochemistry.
RESULTSAfter treatment of 5,7-DHT (PILO + 5,7-DHT group), the success rate, the mortality and the frequency of chronic spontaneous seizures in pilocarpine-induced epilepsy model were all improved. Compared with the control group, the number of serotonergic neuron in raphe nuclei was decrease in PILO + SE group (P < 0.05). Moreover, it's extremely decrease in PILO + 5,7-DHT group (P < 0.01). Compared with control group, the mean escape latency was prolonged, the times of crossing target was decreased and the retention time in target zone was shortened in PILO + SE group (P < 0.05), but there was no significant difference between PILO + SE group and PILO + 5,7-DHT group.
CONCLUSIONDepletion of serotonin may facility the rats' epileptic seizures, but we could not interpret which may cause epileptic rats' cognitive deficit.