Department of Neurobiology, Southern Medical University, Guangzhou, 510515, China.
Mol Neurobiol. 2013 Dec;48(3):794-807. doi: 10.1007/s12035-013-8467-x. Epub 2013 May 8.
Excessive K(+) efflux promotes central neuronal apoptosis; however, the type of potassium channel that mediates K(+) efflux in response to different apoptosis-inducing stimuli is still unknown. It is hypothesized that the activation of large-conductance Ca(2+)-activated K(+) channels (BKCa) mediates hypoxia/reoxygenation (H/R)- and ischemia/reperfusion (I/R)-induced neuronal apoptosis. Rat hippocampal neuronal cultures underwent apoptosis after reoxygenation, as assessed by morphologic observation, terminal deoxynucleotidyl transferase dUTP nick end labeling staining, and caspase-3 activation. Single-channel recordings revealed upregulation of BKCa channel activity 6 h after reoxygenation, which might be caused by elevated cytosolic Ca(2+). The K(+) ionophore valinomycin and the BKCa channel opener NS1619 induced neuronal apoptosis. Transfection of the BKCa channel α subunit into Chinese hamster ovary (CHO-K1) cells, which do not express endogenous K(+) channels, or into neurons will induce cell apoptosis, indicating that the opening of the BKCa channel serves as a pivotal event in mediating cell apoptosis. The specific BKCa channel blockers charybdotoxin and iberiotoxin and the nonselective K(+) channel blocker tetraethylammonium at concentrations more specific to the BKCa channel were neuroprotective. The A-type potassium channel blocker 4-aminopyridine and apamin, a small-conductance Ca(2+)-activated K(+) channel blocker, were not protective. This result suggests the involvement of the BKCa channel in H/R-induced apoptosis. Similarly, specific BKCa channel blockers also showed neuroprotection in neurons subjected to oxygen-glucose deprivation/reoxygenation or animals subjected to forebrain ischemia-reperfusion. These results demonstrate that the over-activity of BKCa channels mediates hippocampal neuronal damage induced by H/R in vitro and I/R in vivo.
细胞外钾离子大量外流会促进中枢神经元凋亡;然而,介导不同凋亡诱导刺激的钾离子外流的钾离子通道类型仍不清楚。据推测,大电导钙激活钾离子通道(BKCa)的激活介导了缺氧/复氧(H/R)和缺血/再灌注(I/R)诱导的神经元凋亡。通过形态学观察、末端脱氧核苷酸转移酶 dUTP 缺口末端标记染色和 caspase-3 激活,评估大鼠海马神经元培养物在复氧后发生凋亡。复氧后 6 小时,单通道记录显示 BKCa 通道活性上调,这可能是由于细胞浆钙离子升高引起的。钾离子载体缬氨霉素和 BKCa 通道开放剂 NS1619 诱导神经元凋亡。将 BKCa 通道 α 亚基转染到不表达内源性钾离子通道的中国仓鼠卵巢(CHO-K1)细胞或神经元中,会诱导细胞凋亡,表明 BKCa 通道的开放是介导细胞凋亡的关键事件。BKCa 通道的特异性阻断剂芋螺毒素和iberiotoxin 以及对 BKCa 通道更具特异性的非选择性钾离子通道阻断剂四乙铵具有神经保护作用。A 型钾离子通道阻断剂 4-氨基吡啶和小电导钙激活钾离子通道阻断剂 apamin 没有保护作用。这一结果表明 BKCa 通道参与了 H/R 诱导的凋亡。同样,特异性 BKCa 通道阻断剂也在氧葡萄糖剥夺/复氧或前脑缺血再灌注的神经元中表现出神经保护作用。这些结果表明,BKCa 通道的过度活跃介导了体外 H/R 诱导的海马神经元损伤和体内 I/R 损伤。