Cortical neuron injury occurs following recurrent epileptiform discharges induced by magnesium-free treatment in vitro.
- Author:
Hai-yan CAO
1
;
Yu-wu JIANG
;
Tao BO
;
Xi-ru WU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Cerebral Cortex; embryology; Culture Media; chemistry; pharmacology; Culture Techniques; Magnesium; pharmacology; Neurons; drug effects; pathology; Rats; Rats, Wistar; Seizures; physiopathology
- From: Chinese Journal of Pediatrics 2003;41(1):25-28
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study cortical neuron injury following recurrent epileptiform discharges induced by magnesium-free treatment in vitro.
METHODSCultured embryo cortical neurons were exposed to magnesium-free media for 3 h, then they were returned to regular media containing normal level magnesium. At different time after Mg(2+)-free treatment, trypan blue staining and determination of LDH activity were used to determine the cell viability, flow cytometry was applied to measure neuronal apoptosis, and MTT assay to study metabolic rate.
RESULTS(1) Neuronal morphology on light microscopy following Mg(2+)-free treatment showed that there were no prominent alterations. (2) At different time (6, 12, 72 h) after Mg(2+)-free treatment, neuronal viability by trypan blue staining and LDH activity showed modest changes compared with time-matched control in different culture days (6, 12, 17 d) (P > 0.05). (3) Cell apoptosis increased mildly at different time after Mg(2+)-free treatment in neurons cultured for different days, but the increase was not significant (P > 0.05). (4) Metabolic rate decreased at 6 h after Mg(2+)-free treatment (P < 0.05) in neurons cultured for 6 d, and was 86.4% of that of the control; while the rate at 24 h in neurons cultured for 12 d and 17 d also decreased (P < 0.05), being 78.7% and 70.9%, respectively, of that of the control.
CONCLUSIONSThese findings demonstrated that the injury occurred on cultured cortical neurons caused by magnesium-free-treatment-induced recurrent epileptiform discharges was mainly functional and relatively mature neurons displayed more severe and much later mitochondrial function impairment than immature neurons.