Characteristic of spontaneous transient outward potassium currents in vascular smooth muscle cells of porcine coronary artery.
- Author:
Fang CAI
1
;
Peng-Yun LI
;
Yan YANG
;
Zhi-Fei LIU
;
Miao-Ling LI
;
Wen ZHOU
;
Jie PEI
;
Jun CHENG
;
Huan LAN
;
Joachim B GRAMMER
;
Xiao-Rong ZENG
Author Information
1. Institute of Myocardial Electrophysiology, Luzhou Medical College, Luzhou 646000, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Coronary Vessels;
cytology;
physiology;
Electrophysiological Phenomena;
physiology;
Muscle, Smooth, Vascular;
cytology;
physiology;
Myocytes, Smooth Muscle;
cytology;
physiology;
Patch-Clamp Techniques;
Potassium Channels, Calcium-Activated;
physiology;
Sodium-Calcium Exchanger;
physiology;
Swine
- From:
Acta Physiologica Sinica
2007;59(1):27-34
- CountryChina
- Language:English
-
Abstract:
Spontaneous transient outward currents (STOCs) play an important role in the myogenic regulation of small artery tone, such as coronary artery. In the present study, we investigated the electrophysiological properties and the regulation of STOCs in vascular smooth muscle cells (VSMCs) of porcine coronary artery by perforated patch-clamp technique. Our data showed that STOCs were dependent on voltage and extracellular calcium and they were highly variable in amplitudes and frequencies. STOCs superimposed stochastically onto whole-cell K(+) currents induced by step and ramp protocols. STOCs were completely abolished by ChTX [inhibitor of large-conductance Ca(2+)-activated potassium (BK(Ca)) channels], removal of extracellular Ca(2+), or addition of ryanodine (50 mumol/L) respectively. In contrast, CdCl2 and verapamil, inhibitors of voltage-dependent L-type Ca(2+) channels, had little effect on STOCs. Caffeine (5 mmol/L) transiently increased STOCs (hump), followed by a temporary inhibition. Ca(2+) ionophore A23187 increased both amplitude and frequency of STOCs. Na(+) ionophore monensin increased the frequency of STOCs. STOCs were strongly inhibited by KB-R7943, a selective inhibitor of the reverse mode of the Na(+)/Ca(2+) exchanger. Based on these observations, we conclude that STOCs are mediated by BK(Ca) channels. The generation and activation of STOCs depend upon Ca(2+) influx through Na(+)/Ca(2+) exchange and release of Ca(2+) from sarcoplasmic reticulum (SR) via ryanodine receptors. This suggests that Na(+)/Ca(2+) exchange determines calcium store refilling. Recycling of entering Ca(2+) from superficial SR may locally elevate Ca(2+) concentration at the plasma membrane, thereby activating BK(Ca) channels and then initiating STOCs.
