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纸质出版日期:2013
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李映新, 黄媛恒, 覃斐章, 等. 17-甲氧基-7-羟基-苯并呋喃查尔酮对心肌细胞内游离钙浓度及L-型钙电流的影响[J]. 中国实验方剂学杂志, 2013,19(15):213-217.
LI Ying-xin, HUANG Yuan-heng, QIN Fei-zhang, et al. Effects of 17-methoxyl-7-hydroxy-benzfuranchalcon on Intracellular Calcium Overload in Cultured Cardiac Myocytes of Neonatal Rats Injured by HO and L-type Calcium Current in Isolated Ventricular Myocytes of Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(15): 213-217.
李映新, 黄媛恒, 覃斐章, 等. 17-甲氧基-7-羟基-苯并呋喃查尔酮对心肌细胞内游离钙浓度及L-型钙电流的影响[J]. 中国实验方剂学杂志, 2013,19(15):213-217. DOI: 10.11653/syfj2013150213.
LI Ying-xin, HUANG Yuan-heng, QIN Fei-zhang, et al. Effects of 17-methoxyl-7-hydroxy-benzfuranchalcon on Intracellular Calcium Overload in Cultured Cardiac Myocytes of Neonatal Rats Injured by HO and L-type Calcium Current in Isolated Ventricular Myocytes of Mice[J]. Chinese journal of experimental traditional medical formulae, 2013, 19(15): 213-217. DOI: 10.11653/syfj2013150213.
目的: 研究17-甲氧基-7-羟基-苯并呋喃查尔酮(YLSC)对H2O2诱导的心肌细胞内钙超载的拮抗作用及对L型钙电流(ICa-L)的影响。 方法: 采用SD 大鼠乳鼠进行心肌细胞培养
实验分为①正常对照组;②H2O2组:上机前加入终浓度为0.3 mmol·L-1 的H2O2;③预先给予低、中、高不同终浓度YLSC药物处理组:分别给予100
200
400 μmol·L-1 YLSC的无血清培养基
孵育24 h
上机前加入终浓度为0.3 mmol·L-1 H2O2
以Fluo-3/AM 荧光指示剂负载
应用激光共聚焦显微镜技术
分别于加入H2O2后15 min内检测细胞内[Ca2+]i的变化;分离昆明种小鼠单个心室肌细胞
全细胞膜片钳技术记录YLSC对ICa-L的影响。 结果: ①与正常对照组比较
H2O2诱导的模型组细胞内[Ca2+]i增加60.43%±7.75%
而高、中、低YLSC预处理组[Ca2+]i分别增加38.39%±13.87%
14.49%±2.94%
-28.1%±1.52%
与模型组比较显著降低(P<0.01)。②YLSC可使心室肌细胞ICa-L的电流-电压(I-V)关系曲线上移
能改变ICa-L的激活和失活特征
使ICa-L的激活曲线和稳态失活曲线左移。 结论: YLSC对心肌细胞钙离子通道有较好的阻断作用
能显著减轻H2O2诱导的心肌细胞内[Ca2+]i超载。
Objective: To investigate the effects of 17-methoxyl-7-hydroxy-benzfuranchalcon (YLSC)on intracellular calcium overload in cultured cardiac myocytes of neonatal rats injured by H2O2and L-type calcium current(ICa-L) in isolated ventricular myocytes. Method: The cells of primary cultured cardiac myocytes of neonatal rats were divided into groups:①control group;② model group:administrated with 0.3 mmol·L-1 H2O2;③YLSC treated groups:incubation respectively with 100
200
400 μmol·L-1YLSC for 24 h
and add 0.3 mmol·L-1 H2O2.Laser confocal microscopy was used with Fluo-3/Am as indicator to detect changes of [Ca2+]i immediately and 15 mintues after H2O2 intervention. Single ventricular cell was obtained enzymatically by Langendorff perfusion apparatus. The wholecell patch clamp was used to record the ICa-L. Result: ①The average fluorescence intensity values of the model group treated by H2O2 higher significantly than control group and the fluorescence enhancement ratio was 60.43%±7.75%. The YLSC could decline the intensity values in a does-dependent manner manner
the fluorescence enhancement ratios of low
middle and high does respectively were 38.39%±13.87%
14.49%±2.94%
-28.1%±1.52%
and all of them were much lower compared with H2O2 group(P<0.01). ②YLSC can up-shifted the current-voltage(I-V) curves and markedly shifted the steady state activation and inactivation curve of ICa-L to the left. Conclusion: YLSC inhibited the L-type calcium channel
it can significantly reduce the myocardial intracellular Ca2+ overload induced by H2O2.
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