首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Two different inward rectifier K~+ channels are effectors for transmitter-induced slow excitation in brain neurons
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Two different inward rectifier K~+ channels are effectors for transmitter-induced slow excitation in brain neurons

机译:两种不同的内向整流器K〜+通道是脑神经元中发射器诱导的缓慢激发的效应子

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Substance P (SP) excites large neurons of the nucleus basalis (NB) by inhibiting an inward rectifier K~+ channel (Kir). The properties of the Kir in NB (KirNB) in comparison with the G protein-coupled Kir (GIRK) were investigated. Single-channel recordings with the cell-attached mode showed constitutivefy active KirNB channels, which were inhibited by SP. When the recording method was changed from the on-cell to the inside-out mode, the channel activity of KirNB remained intact with its constitutive activity unaltered. Application of Gβ_(1γ2) to inside-out patches induced activity of a second type of Kir (GIRK). Application of Gβ_(1γ2), however, did not change the KirNB activity. Sequestering Gβ_(1γ2) with Gα_(i2) abolished the GIRK activity, whereas the KirNB activity was not affected. The mean open time of KirNB channels (1.1 ms) was almost the same as that of GIRKs. The unitary conductance of KirNB was 23 pS (155 mM [K~+]_o), whereas that of the GIRK was larger (32-39 pS). The results indicate that KirNB is different from GIRKs and from any of the classical Kirs (IRKs). Whole-cell current recordings revealed that application of muscarine to NB neurons induced a GIRK current, and this GIRK current was also inhibited by SP. Thus, SP inhibits both KirNB and GIRKs. We conclude that the excitatory transmitter SP has two types of Kirs as its effectors: the constitutively active, Gβγ-independent KirNB channel and the Gβγ-dependent GIRK.
机译:P(SP)物质通过抑制向内整流器K +通道(Kir)激发基底核(NB)的大神经元。与G蛋白偶联的Kir(GIRK)相比,研究了NB中Kir的特性(KirNB)。具有细胞附着模式的单通道记录显示了本构激活的KirNB通道,该通道被SP抑制。当将记录方法从“ on-cell”模式更改为“ inside-out”模式时,KirNB的通道活性保持不变,其组成活性不变。将Gβ_(1γ2)应用于由内而外的贴剂可诱导第二种Kir(GIRK)的活性。然而,Gβ_(1γ2)的应用并没有改变KirNB活性。用Gα_(i2)螯合Gβ_(1γ2)消除了GIRK活性,而KirNB活性未受影响。 KirNB通道的平均打开时间(1.1毫秒)与GIRK的平均打开时间几乎相同。 KirNB的单位电导为23 pS(155 mM [K〜+] _ o),而GIRK的单位电导更大(32-39 pS)。结果表明,KirNB与GIRK和任何经典的Kirs(IRK)不同。全细胞电流记录显示,将毒蕈碱应用于NB神经元会诱导GIRK电流,而该GIRK电流也被SP抑制。因此,SP同时抑制KirNB和GIRK。我们得出的结论是,兴奋性递质SP具有两种类型的Kirs作为其效应子:本构活性的,Gβγ独立的KirNB通道和Gβγ依赖的GIRK。

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