Change of neurocytes in acute intoxicated encephalopathy induced by 1, 2-dichloroethane after intervention with antagonists.
- Author:
Jing WANG
1
;
Mao-Long GAO
;
Ying-Tao SHI
;
Qiao NIU
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Calcium; antagonists & inhibitors; physiology; Cells, Cultured; Ethylene Dichlorides; toxicity; Neurons; drug effects; pathology; Rats; Rats, Sprague-Dawley; Receptors, N-Methyl-D-Aspartate; antagonists & inhibitors; physiology
- From: Chinese Journal of Industrial Hygiene and Occupational Diseases 2007;25(12):726-729
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo study the role of N-methyl-D-aspartate receptor and Ca(2+) in acute intoxicated encephalopathy induced by 1, 2-dichloroethane (1, 2-DCE) in vitro.
METHODSNeurocytes of new born rats were cultured in vitro, which were administered with different doses of 1, 2-DCE, and NMDAR and Ca(2+) antagonists including Ketamine and Nimodiping respectively. The cell morphologic structures were observed under light microscope, and its proliferation was detected by Cell Counting Kit-VIII.
RESULTS1, 2-DCE could damage the normal morphological structure of neurocytes: the cell body swelled and broke down, the karyon slurred or disappeared, the axone became shorten and thick, connection of neurocytes was reduced, the cell membrane was half-baked, injury of neurocytes became severer with the increase of the dose of 1, 2-DCE. There was no statistical difference in the proliferation of neurocytes between every 1, 2-DCE groups (P > 0.05), but there was significantly statistical difference between 1, 2-DCE groups, the control group, and the retarder groups (P < 0.01).
CONCLUSION1, 2-DCE can damage the normal morphological structure of neurocytes, and the damage will become severer with the increase of the dose of 1, 2-DCE. However, the cell morphologic structures and proliferation of antagonist groups are much better than those in the 1, 2-DCE groups.