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首页> 外文期刊>Neuroreport >Nociceptin/orphanin FQ-induced inhibition of delayed rectifier potassium currents by calcium/calmodulin-dependent protein kinase type II.
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Nociceptin/orphanin FQ-induced inhibition of delayed rectifier potassium currents by calcium/calmodulin-dependent protein kinase type II.

机译:Nociceptin / orphanin FQ对钙/钙调蛋白依赖性蛋白激酶II型的延迟整流钾电流的抑制作用。

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The neuropeptide nociceptin/orphanin FQ (N/OFQ) has been shown to inhibit delayed rectifier potassium current (IK) in acutely dissociated rat parietal cortical neurons. However, the detailed mechanism of N/OFQ-induced inhibition on IK is not clear. This study is the first to explore an involvement of calcium/calmodulin (CaM)-dependent protein kinase type II (CaMKII) in mediating N/OFQ-induced responses. Utilizing pharmacological inhibitors of CaM and CaMKII, we have investigated the contribution of CaMKII in N/OFQ-induced effects using the whole-cell patch-clamp technique. In whole-cell voltage clamp, W-7 (100?μM), an antagonist of CaM, as well as KN-62, an inhibitor of CaMKII activity, attenuated the inhibitory effects of N/OFQ on IK. Activation and inactivation analysis indicated that the kinetics of IK were altered by N/OFQ, with decreased activation and promoted inactivation of IK. W-7 and KN-62 (10?μM) partly abolished the activation and inactivation curves shift of IK induced by N/OFQ. These findings show that CaMKII plays a critical role in N/OFQ-induced inhibition of IK in acutely dissociated rat parietal cortical neurons.
机译:已经显示神经肽伤害感受器/孤儿蛋白FQ(N / OFQ)可以抑制急性解离的大鼠顶叶皮层神经元的延迟整流钾电流(IK)。但是,N / OFQ诱导的IK抑制作用的详细机制尚不清楚。这项研究是第一个探索钙/钙调蛋白(CaM)依赖性II型蛋白激酶(CaMKII)在介导N / OFQ诱导的反应中的参与。利用CaM和CaMKII的药理抑制剂,我们使用全细胞膜片钳技术研究了CaMKII在N / OFQ诱导的效应中的作用。在全细胞电压钳中,CaM的拮抗剂W-7(100?μM)以及CaMKII活性的抑制剂KN-62减弱了N / OFQ对IK的抑制作用。活化和失活分析表明,N / OFQ改变了IK的动力学,降低了IK的活化并促进了IK的失活。 W-7和KN-62(10?M)消除了N / OFQ诱导的IK的激活和失活曲线移动。这些发现表明,CaMKII在N / OFQ诱导的急性分离大鼠顶叶皮层神经元的IK抑制中起关键作用。

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