Aihara Yasuo, Jahromi Babak S, Yassari Reza, Nikitina Elena, Agbaje-Williams Mayowa, Macdonald R Loch
Department of Surgery, University of Chicago and Pritzker School of Medicine, Chicago, IL 60637, USA.
J Cereb Blood Flow Metab. 2004 Jan;24(1):75-83. doi: 10.1097/01.WCB.0000095803.98378.D8.
Cerebral vasospasm is a transient, delayed constriction of cerebral arteries that occurs after subarachnoid hemorrhage (SAH). Smooth muscle cells show impaired relaxation after SAH, which may be caused by a defect in the ionic mechanisms regulating smooth muscle membrane potential and Ca(2+) permeability. We tested this hypothesis by examining changes in expression of mRNA and protein for ion channels in the basilar arteries of dogs after SAH using quantitative real-time polymerase chain reaction (PCR) and western blotting. SAH was associated with a significant reduction in basilar artery diameter to 41 +/- 8% of pre-SAH diameter (P < 0.001) after 7 days. There was significant downregulation of the voltage-gated K(+) channel K(v) 2.2 (65% reduction in mRNA, P < 0.001; 49% reduction in protein, P < 0.05) and the beta1 subunit of the large-conductance, Ca(2+) - activated K(+) (BK) channel (53% reduction in mRNA, P < 0.02). There was no change in BK beta1 subunit protein. Changes in mRNA levels of K(v) 2.2 and the BK-beta1 subunit correlated with the degree of vasospasm (r(2) = 0.490 and 0.529 respectively, P < 0.05). The inwardly rectifying K(+) (K(ir)) channel K(ir) 2.1 was upregulated (234% increase in mRNA, P < 0.001; 350% increase in protein, P < 0.001). There was no significant change in mRNA expression of L- type Ca(2+) channels and the BK-alpha subunit. These data suggest that K(+) channel dysfunction may contribute to the pathogenesis of cerebral vasospasm.
脑血管痉挛是蛛网膜下腔出血(SAH)后发生的脑动脉短暂性延迟收缩。SAH后平滑肌细胞舒张功能受损,这可能是由调节平滑肌膜电位和Ca(2+)通透性的离子机制缺陷引起的。我们通过定量实时聚合酶链反应(PCR)和蛋白质印迹法检测SAH后犬基底动脉中离子通道mRNA和蛋白质表达的变化,来验证这一假设。SAH后7天,基底动脉直径显著缩小至SAH前直径的41±8%(P<0.001)。电压门控K(+)通道K(v) 2.2显著下调(mRNA减少65%,P<0.001;蛋白质减少49%,P<0.05),大电导Ca(2+)激活K(+)(BK)通道的β1亚基也显著下调(mRNA减少53%,P<0.02)。BKβ1亚基蛋白质无变化。K(v) 2.2和BK-β1亚基的mRNA水平变化与血管痉挛程度相关(r(2)分别为0.490和0.529,P<0.05)。内向整流K(+)(K(ir))通道K(ir) 2.1上调(mRNA增加234%,P<0.001;蛋白质增加350%,P<0.001)。L型Ca(2+)通道和BK-α亚基的mRNA表达无显著变化。这些数据表明,K(+)通道功能障碍可能在脑血管痉挛的发病机制中起作用。