Feng Jun, Liu Yuhong, Khabbaz Kamal R, Sodha Neel R, Osipov Robert M, Hagberg Robert, Alper Seth L, Sellke Frank W
Department of Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
J Surg Res. 2009 Nov;157(1):123-8. doi: 10.1016/j.jss.2009.03.043. Epub 2009 May 3.
We investigated the role of calcium-activated potassium (K(Ca)) channel activation in myogenic tone in human peripheral microvasculature after heart surgery.
Human skeletal muscle arterioles (90-180microm diameter) were dissected from tissue harvested pre- and post-cardiopulmonary bypass (CPB) during cardiac surgery. Myogenic reactivity in response to stepwise increases in intraluminal pressure was studied between pressure steps. Microvessel tone was determined pre-CPB, post-CPB, and after blockade of K(Ca) channels. Expression and localization of large conductance (BK) K(Ca) channels in the coronary microvasculature was assessed by immunoblot and immunofluorescence photomicroscopy.
Myogenic tone of skeletal muscle arterioles was significantly reduced post-CPB compared with pre-CPB. Decrease in myogenic tone after CPB was reflected by the increase in microvessel internal diameter. Myogenic tone of post-CPB microvessels was significantly increased after treatment with BK(Ca)-blocker iberiotoxin, but unchanged in the combined presence of the blockers of intermediate (IK(Ca)) and small conductance (SK(Ca)) K(Ca) channels, TRAM34/apamin. The increases in myogenic tone after iberiotoxin treatment were demonstrated as a decrease in microvessel internal diameter. No significant differences in BK(Ca) protein levels were noted comparing pre- and post-CPB conditions judged by immunoblot and by immunofluorescence staining of skeletal muscle microvessels. Prominent staining for BK(Ca)-alpha and BK(Ca)-beta(1) subunits localized to the microvascular smooth muscle.
CPB-associated decrease in peripheral myogenic reactivity is likely due to activation of BK(Ca), but not IK(Ca) or SK(Ca). CPB may increase BK(Ca) activity without increasing BK polypeptide level.
我们研究了钙激活钾(K(Ca))通道激活在心脏手术后人体外周微血管肌源性张力中的作用。
在心脏手术期间,从体外循环(CPB)前后采集的组织中解剖出人体骨骼肌小动脉(直径90 - 180微米)。研究了在压力阶跃之间,内腔压力逐步升高时的肌源性反应性。在CPB前、CPB后以及阻断K(Ca)通道后测定微血管张力。通过免疫印迹和免疫荧光显微镜评估大电导(BK)K(Ca)通道在冠状动脉微血管中的表达和定位。
与CPB前相比,CPB后骨骼肌小动脉的肌源性张力显著降低。CPB后肌源性张力的降低通过微血管内径的增加得以体现。用BK(Ca)阻滞剂iberiotoxin处理后,CPB后微血管的肌源性张力显著增加,但在同时存在中间电导(IK(Ca))和小电导(SK(Ca))K(Ca)通道阻滞剂TRAM34/蜂毒明肽的情况下,肌源性张力无变化。iberiotoxin处理后肌源性张力的增加表现为微血管内径的减小。通过免疫印迹以及骨骼肌微血管的免疫荧光染色判断,CPB前后BK(Ca)蛋白水平无显著差异。BK(Ca)-α和BK(Ca)-β(1)亚基的显著染色定位于微血管平滑肌。
CPB相关的外周肌源性反应性降低可能是由于BK(Ca)的激活,而非IK(Ca)或SK(Ca)。CPB可能增加BK(Ca)活性而不增加BK多肽水平。