首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Direct blockade of both cloned rat rod photoreceptor cyclic nucleotide-gated non-selective cation (CNG) channel alpha-subunit and native CNG channels from Xenopus rod outer segments by H-8, a non-specific cyclic nucleotide-dependent protein kinase in
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Direct blockade of both cloned rat rod photoreceptor cyclic nucleotide-gated non-selective cation (CNG) channel alpha-subunit and native CNG channels from Xenopus rod outer segments by H-8, a non-specific cyclic nucleotide-dependent protein kinase in

机译:H-8是非特异性环状核苷酸依赖性蛋白激酶H-8,可直接阻断非洲爪蟾杆外部片段对大鼠杆状光感受器环状核苷酸门控非选择性阳离子(CNG)通道α亚基和天然CNG通道的直接阻断

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摘要

Using excised inside-out patch techniques, a non-specific cyclic nucleotide-dependent protein kinase inhibitor, H-8 (N-2-(methylamino)ethyl-5-isoquinolinesulfonamide), has been shown to suppress directly the activities of both rat rod photoreceptor cyclic GMP-gated channel alpha-subunits expressed in Xenopus oocytes and native cGMP-gated channels from Xenopus rod outer segments. When co-applied with 100 microM cGMP on the cytoplasmic side of the patches, current suppression by H-8 increased with membrane depolarization. Blockade by H-8 was not relieved by supersaturating concentrations of cGMP (1 mM). In addition, blockade by H-8 showed significant inhibition of channel activity at negative holding potentials when acting from the extracellular side of the channel. The results were consistent with the conclusion that H-8 can act as an open channel blocker from either side of the channel. Even though H-8 is a much more effective kinase inhibitor, it is frequently used at concentrations that cause inhibition of cGMP-gated channels and this effect needs to be taken into account when evaluating results obtained with this compound.
机译:已经证明,使用切除的内而外贴片技术,非特异性环状核苷酸依赖性蛋白激酶抑制剂H-8(N-2-(甲基氨基)乙基-5-异喹啉基磺酰胺)可直接抑制两个大鼠杆的活性。在非洲爪蟾卵母细胞中表达的光感受器环状GMP门控通道α亚基和非洲爪蟾杆外部节段的天然cGMP门控通道。当与100 microM cGMP共同应用在贴片的细胞质侧时,H-8的电流抑制随着膜去极化而增加。过高浓度的cGMP(1 mM)无法消除H-8的封锁。此外,当从通道的细胞外作用时,被H-8阻断可在负保持电位下显着抑制通道活性。结果与以下结论一致:H-8可以从通道的任何一侧充当开放通道的阻止者。即使H-8是一种更有效的激酶抑制剂,它也经常以导致抑制cGMP门控通道的浓度使用,在评估使用该化合物获得的结果时,必须考虑到这种影响。

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