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
|更新时间:2024-01-04
|
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
Chinese Journal of Experimental Traditional Medical FormulaeVol. 19, Issue 15, Pages: 213-217(2013)
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:
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.
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
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.