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冷血心肌麻痹液温度与SR Ca^(2+)-ATPase活性及SR Ca^(2+)-ATPase mRNA表达 被引量:2

Effect of temperature on SR Ca 2+ ATPase activity and SR Ca 2+ ATPase mRNA expression during cold blood cardioplegic arrest
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摘要 目的:评价冷血心肌麻痹液( C B C)温度对心肌保护效果的影响. 方法:离体鼠心经 C B C不同温度(4,8,12,16 和20℃)停搏120 m in 及再灌注60 m in, 测定心肌肌浆网( S R) Ca2+  A T Pase 活性、钙摄取和 S R Ca2+  A T Pase m R N A 表达的改变. 结果:4,8,12℃组 S R Ca2+  A T Pase 活性、钙摄取保护优于16 和20℃组( P< 0.01),4℃~16℃组 S R Ca2+  A T Pase m R N A 表达量为对照组1.18~1.32 倍( P> 0.05),20℃组表达量为对照组的 1.63 倍( P< 0.05). 结论:温度影响 C B C心肌保护效果, S R Ca2+  A T Pase m R N A 表达上调可能与 S R泵功能受损的特异修复机制有关. AIM: To evaluate the effect of temperature on myocardial protection during cold blood cardioplegic arrest. METHODS: Working hearts isolated from rats underwent 120 minutes of hypothermic blood cardioplegic arrest, during which myocardial temperatures were maintained at 4℃, 8℃, 12℃, 16℃ and 20℃ respectively. Alterations in sarcoplasmic reticulum (SR) Ca 2+ ATPase activity, Ca 2+ uptake and expression of SR Ca 2+ ATPase mRNA were assessed. RESULTS: SR Ca 2+ ATPase activity and Ca 2+ uptake in groups of 4℃, 8℃ and 12℃ were well maintained, which had better protective effects than those in groups of 16℃ and 20℃ ( P <0.01). Expression of SR Ca 2+ ATPase mRNA in groups of 4℃, 8℃, 12℃ and 16℃ did not increase significantly as compared with that of control group( P >0.05). However, upregulation of SR Ca 2+ ATPase mRNA in 20℃ group increased by 1.6 times ( P <0.05). CONCLUSION: Temperature has potential effects on myocardial protection during cold blood cardioplegic arrest. Protective efficacy attained by hypothermic arrest at temperatures from 4℃~12℃ may couple the provision of myocardial aerobic metabolism with the capacity to lower myocardial oxygen demands for arrested hearts. The upregualtion of SR Ca 2+ ATPase mRNA expression may suggest the specific repair mechanism of the impaired cardiac SR pump.
出处 《第四军医大学学报》 1999年第9期809-811,共3页 Journal of the Fourth Military Medical University
关键词 心麻痹液 温度 肌浆网 RNA mRNA ATP酶 cardioplegic solutions temperature sarcoplasmic reticulum RNA messenger
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