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Neuroprotective Effect of Lithium Chloride in Rat Model of Cardiac Arrest
Author(s) -
И. В. Острова,
О. А. Гребенчиков,
Н. В. Голубева
Publication year - 2019
Publication title -
obŝaâ reanimatologiâ
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.175
H-Index - 6
eISSN - 2411-7110
pISSN - 1813-9779
DOI - 10.15360/1813-9779-2019-3-73-82
Subject(s) - neuroprotection , lithium chloride , resuscitation , lithium (medication) , hippocampal formation , hippocampus , saline , anesthesia , medicine , endocrinology , chemistry , pharmacology , organic chemistry
Lithium chloride, which is used for the treatment of bipolar disorders, has a neuroprotective eect in conditions associated with acute and chronic circulatory disorders. The purpose of the study : to investigate the ecacy of lithium chloride for the prevention of post-resuscitation death of hippocampal neurons during the post-resuscitation period. Material and methods . Cardiac arrest for 10 minutes was evoked in mature male rats by intrathoracic clumping of the vascular bundle of the heart, followed by resuscitation. 40 mg/kg or 20 mg/kg of 4,2% lithium chloride (LiCl) was injected intraperitoneally 1 hour before cardiac arrest, on the 1st and 2nd day after resuscitation (n=9). Untreated animals received equivalent doses of saline (n=9). Rats after a sham surgery served as a reference group (n=10). The number of viable neurons in the CA1 and CA3/CA4 elds of the hippocampus was estimated in slides stained with cresyl violet by day 6 or 7 postresuscitation. In a separate series of experiments, at the same terms, we studied the eect of lithium chloride on the protein content of GSK3β (glycogen synthase kinase) in brain tissue using Western-Blot analysis. Results.  Histological assay showed that a 10-minute cardiac arrest resulted in a decrease in the number of viable neurons in the hippocampal CA1 eld — by 37.5% (P0.001), in the CA3/CA4 eld — by 12.9% (P0.05) vs. the reference group. Lithium treatment increased the number of viable neurons in resuscitated rats — in the CA1 eld by 37% (P<0.01), in the CA3/CA4 eld — by 11.5% (P0.1) vs. the untreated animals. It was found that lithium caused an increase in phosphorylated form of GSK3β: by 180% vs. the reference group (P[1]0.05), and by 150% vs. the untreated animals (P0.05). Conclusion . Lithium treatment leads to a pronounced neuroprotection in the neuronal populations of the hippocampus post-resuscitation. This eect may be due to an increase in the content of the phosphorylated form of GSK3β protein. The results indicate a high potential of lithium for the prevention and treatment of neurodegenerative disorders caused by a temporary arrest of blood circulation. 

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