scholarly journals Interconversion between distinct gating pathways of the high threshold calcium channel in rat ventricular myocytes.

1993 ◽  
Vol 462 (1) ◽  
pp. 197-228 ◽  
Author(s):  
S Richard ◽  
P Charnet ◽  
J M Nerbonne
2008 ◽  
Vol 86 (9) ◽  
pp. 620-625 ◽  
Author(s):  
Ru-xing Wang ◽  
Wen-ping Jiang

To investigate the effects of S- and R-amlodipine (Aml) on action potential (AP) and L-type calcium channel current (ICa-L), the whole-cell patch-clamp technique was used on rat ventricular myocytes to record AP, ICa-L, peak currents, steady-state activation currents, steady-state inactivation currents, and recovery currents from inactivation with S-Aml and R-Aml at various concentrations. Increasing concentrations of S-Aml gradually shortened AP durations (APDs). At concentrations of 0.1, 0.5, 1, 5, and 10 μmol/L, S-Aml blocked 1.5% ± 0.2%, 25.4% ± 5.3%, 65.2% ± 7.3%, 78.4% ± 8.1%, and 94.2% ± 5.0% of ICa-L, respectively (p < 0.05), and the half-inhibited concentration was 0.62 ± 0.12 µmol/L. Current–voltage curves were shifted upward; steady-state activation and inactivation curves were shifted to the left. At these concentrations of S-Aml, the half-activation voltages were –16.01 ± 1.65, –17.61 ± 1.60, –20.17 ± 1.46, –21.87 ± 1.69, and –24.09 ± 1.87 mV, respectively, and the slope factors were increased (p < 0.05). The half-inactivation voltages were –27.16 ± 4.48, –28.69 ± 4.52, –31.19 ± 4.17, –32.63 ± 4.34, and –35.16 ± 4.46 mV, respectively, and the slope factors were increased (p < 0.05). The recovery times from inactivation of S-Aml were prolonged (p < 0.05). In contrast, R-Aml had no effect on AP and ICa-L (p > 0.05) at the concentrations tested. Thus, only S-Aml has calcium channel blockade activity, whereas R-Aml has none of the pharmacologic actions associated with calcium channel blockers.


2010 ◽  
Vol 31 (11) ◽  
pp. 1438-1446 ◽  
Author(s):  
An-tao Luo ◽  
Hong-yan Luo ◽  
Xin-wu Hu ◽  
Lin-lin Gao ◽  
Hua-min Liang ◽  
...  

2012 ◽  
Vol 35 (8) ◽  
pp. 1249-1256 ◽  
Author(s):  
Hong Xin ◽  
Ming Gu ◽  
Wen Wei Wang ◽  
Shi Ying Huang ◽  
Fang Ping Li ◽  
...  

2003 ◽  
Vol 285 (3) ◽  
pp. E449-E453 ◽  
Author(s):  
Kish L. Golden ◽  
James D. Marsh ◽  
Yang Jiang ◽  
Tiane Brown ◽  
Jerome Moulden

Sex-related differences in cardiac function have been well documented. The extent to which sex hormones are responsible for these differences is unclear. The current study was designed to determine whether castration and androgen replacement resulted in changes in functional expression of genes encoding the L-type calcium channel and Na/Ca exchanger in isolated rat ventricular myocytes. Sixteen weeks of castration produced a 50% decline in dihydropyridine receptor expression levels and a 16% ( P < 0.05) increase in time to peak shortening. Furthermore, cardiac myocytes isolated from castrated animals also displayed an 18% ( P < 0.001) increase in time to relengthening and an 80% decrease in Na/Ca exchanger gene expression when compared with intact controls. Testosterone treatment of castrated animals completely reversed these effects. These results provide the first evidence that androgens regulate functional expression of the L-type calcium channel and the Na/Ca exchanger in isolated rat ventricular myocytes and thus may play a role in modulating cardiac performance in males and thereby contribute to the observed gender differences in cardiac function.


Endocrinology ◽  
2009 ◽  
Vol 150 (8) ◽  
pp. 3726-3734 ◽  
Author(s):  
Andrés Maturana ◽  
Sébastien Lenglet ◽  
Magaly Python ◽  
Shun'Ichi Kuroda ◽  
Michel F. Rossier

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