PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2
中国医学科学杂志(英文版)2003年0卷第4期 页码:260-264
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PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2
Affiliations:
1. Li Yuan 1,,Zheng Yansong 2 ,Gong Weiqin 1 and Wang Xiaoming 1 1 Department of Geriatrics,Xijing Hospital,Fourth Military Medical University,Xi ’an710032 2 Department of Geriatrics,Chinese PLA General Hospital,Beijing,100853
2. Xijing Hospital
3. Fourth Military Medical University
4. Xi ’an,710032
5. Chinese PLA General Hospital
6. ,China
Author bio:
Funds:
DOI:
中图分类号:R96
纸质出版日期:2003
Accepted:
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PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2[J]. 中国医学科学杂志(英文版), 2003,0(4):260-264.
PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2[J]. Chinese medical sciences journal, 2003, 0(4): 260-264.
PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2[J]. 中国医学科学杂志(英文版), 2003,0(4):260-264.DOI:
PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2[J]. Chinese medical sciences journal, 2003, 0(4): 260-264.DOI:
PROTECTIVE EFFECTS OF MELATONIN ON CULTURED RAT CARDIOMYOCYTES DAMAGED BY H2O2
摘要
Abstract
Objective.To investigate the protective effects of melatonin(MT )on cardiomyocytes against the ox-idative injury induced by H 2 O 2 .Methods.Ventricular myocytes were isolated from neonatal rats and cultured for3~5days.Cells were divided into4groups:control group
H 2 O 2 (100μmol/L H 2 O 2 )group
MT group(100μmol/L MT )and MT preconditioning group(100μmol/L MT+100μmol/L H 2 O 2 ).The fluorescent probe
DCFH?DA
was used to detect intracellular levels of reactive oxygen species(ROS)and another fluorescent probe
Fluo-3?AM
was used to detect[Ca 2+ ] i by using a laser scanning confocal microscopy(LSCM).The malondi-aldehyde(MDA)content in cardiomyocytes was determined by measuring thiobarbituric acid?reactive sub-stances to monitor lipid peroxidation.The activity of cytoplasmic enzyme lactate dehydrogenase(LDH)that was released into the culture media was assayed to indicate alternation in the integrity of the cellular membrane.Trypan blue exclusion was used to detect the cell viability.Results.Compared with the control group
intracellular ROS
[Ca 2+ ] i
MDA content
LDH leakage and cell death were significantly elevated when cells were treated by100μmol/L H 2 O 2 for60minutes(P<0.01).However
those changes were significantly attenuated in MT preconditioning group.Conclusion.MT has very good antioxidant effect and can protect the cardiomyocytes against H 2 O 2 -in-duced injury.