钙库调控的钙离子通道对大鼠膀胱平滑肌收缩性调控的研究

赵滨; 白新宇; 董兴有; 王青青; 李龙坤; 宋波

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钙库调控的钙离子通道对大鼠膀胱平滑肌收缩性调控的研究

论著 | 更新时间：2025-01-15

- 钙库调控的钙离子通道对大鼠膀胱平滑肌收缩性调控的研究
- Store operated calcium channels regulate contraction of rat bladder smooth muscle in vitro
- 陆军军医大学学报 2014年36卷第11期页码：1178-1182
- 作者机构：
  
  1. 第三军医大学西南医院泌尿外科
  2. 第三军医大学新桥医院泌尿外科
- 作者简介：
- 基金信息：
- DOI：
  中图分类号： R322.62;R329.25;R-332
- 纸质出版日期：2014，
  
  网络出版日期：2014-06-15，
- 稿件说明：
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赵滨, 白新宇, 董兴有, 等. 钙库调控的钙离子通道对大鼠膀胱平滑肌收缩性调控的研究[J]. 陆军军医大学学报, 2014,36(11):1178-1182.

ZHAO BIN, BAI XINYU, DONG XINYOU, et al. Store operated calcium channels regulate contraction of rat bladder smooth muscle in vitro. [J]. Journal of army medical university, 2014, 36(11): 1178-1182.
赵滨, 白新宇, 董兴有, 等. 钙库调控的钙离子通道对大鼠膀胱平滑肌收缩性调控的研究[J]. 陆军军医大学学报, 2014,36(11):1178-1182. DOI：

ZHAO BIN, BAI XINYU, DONG XINYOU, et al. Store operated calcium channels regulate contraction of rat bladder smooth muscle in vitro. [J]. Journal of army medical university, 2014, 36(11): 1178-1182. DOI：

摘要

目的分析胞内钙库调控的钙离子通道（store operated calcium channels

SOCCs）在大鼠膀胱平滑肌中的功能。方法 RT-PCR检测SOCCs相关蛋白基因表达；使用SOCCs的激动剂CPA（10 μmol/L）以及抑制剂SKF-96365（10 μmol/L），采用离体肌条的方法观察其肌肉的收缩，全细胞膜片钳技术观察膀胱平滑肌细胞电流，激光共聚焦显微镜观察其膀胱平滑肌细胞内钙离子变化。结果 RT-PCR检测到TRPC3、TRPC4和STIM1基因表达。加入CPA激活SOCCs后，离体肌条实验结果显示膀胱平滑肌离体肌条收缩频率为（5.937 5±1.108 0）/min，比加入CPA前明显增加(

0.05)，收缩幅度为（0.067 1±0.027 0）g，比加入CPA前明显降低(

0.05)；膜片钳实验结果显示钙电流较加入CPA前显著增加，-80 mV电流密度为（-3.127 1±0.908 7）pA/pF，20 mV电流密度为（1.048 1±0.322 5）pA/pF(

0.05)；激光共聚焦显微镜实验结果显示钙离子相对荧光（1.150 7±0.212 1）较加入CPA前显著增加（

0.05）。加入抑制剂SKF-96365抑制SOCCs后，离体肌条收缩频率为（5.081 3±1.129 5）/min，较加入CPA后显著减缓(

0.05)，收缩幅度为（0.079 0±0.033 0）g，较加入CPA后显著增加(

0.05)；膜片钳显示钙电流较加入CPA后显著减少，-80 mV电流密度为（-2.678 1±0.804 4）pA/pF，20 mV电流密度为（0.907 7±0.346 2）pA/pF(

0.05)；激光共聚焦显微镜实验结果显示细胞内钙离子相对荧光（1.028 9±0.204 7）较加入CPA后显著减少（

0.05)。结论膀胱平滑肌中可以表达SOCCs相关的通道，膀胱平滑肌的收缩性受到SOCCs的影响。

Abstract

Objective To investigate the function of intracellular store operated calcium cha

nnels (SOCCs) in the contraction of bladder smooth muscle of rats. Methods Bladder smooth muscle cells (BSMCs) and bladder smooth muscle strips were isolated from female SD rats. RT-PCR was employed to detect the expression of the SOCCs related genes in the bladder tissues. The SOCCs agonist CPA (10 μmol/L) and its inhibitor SKF-96365 (10 μmol/L) was used to treat the isolated BSMCs and muscle stripes. The isolated bladder smooth muscle was used for contraction

in vitro

. The cell current was recorded with whole-cell patch-clamp technique. The changes of intracellular calcium ion were observed by lacer scanning confocal microscopy. Results TRPC3

TRPC4 and STIM1 were expressed in BSMCs. CPA treatment resulted in significant increase in the contraction frequency (5.937 5±1.108 0 times/min) and obvious decrease in the amplitude (0.067 1±0.027 0 g) of the isolated muscle strips (

0.05). Whole-cell patch-clamp technique indicated that CPA treatment induced obvious increase in the cell calcium currents

with the current destiny of -3.127 1±0.908 7 pA/pF at -80 mV and 1.048 1±0.322 5 pA/pF at 20 mV (

0.05). The relative intensity of fluorescence was significant enhanced (1.150 7±0.212 1) than the cells without treatment (

0.05). On the contrary

the use of SKF-96365 decreased the contraction frequency to 5.081 3±1.129 5 times/min and increased amplitude to 0.079 0±0.033 0 g of the bladder smooth muscle strips

both with significant difference with the addition of CPA (

0.05). The calcium currents became little compared with that induced by CPA treatment

and the current destiny was -2.678 1±0.804 4 pA/pF at -80 mV and 0.907 7±0.346 2 pA/pF at 20 mV (

0.05). The relative intensity of fluorescence was also significantly reduced (1.028 9±0.204 7) compared with the treatment of CPA (

0.05). Conclusion The bladder smooth muscle expresses SOCCs

and its contraction is affected by the channels.

关键词

钙库调控的钙离子通道膀胱平滑肌钙离子

Keywords

store operated calcium channelsbladder smooth musclecalcium ions

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