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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >The distribution of small and intermediate conductance calcium-activated potassium channels in the rat sensory nervous system.
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The distribution of small and intermediate conductance calcium-activated potassium channels in the rat sensory nervous system.

机译:小和中等电导钙激活钾通道在大鼠感觉神经系统中的分布。

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Small (SK) and intermediate (IK) conductance calcium-activated potassium channels are candidate ion channels for the regulation of excitability in nociceptive neurones. We have used unique peptide-directed antisera to describe the immunocytochemical distribution of the known isoforms of these ion channels in dorsal root ganglia (DRG) and spinal cord of the rat. These investigations sought to characterize further the phenotype and hence possible functions of nociceptive neurone subpopulations in the rat. In addition, using Western blotting, we sought to determine the level of protein expression of SK and IK channels in sensory nervous tissues following induction of inflammation (Freund's Complete Adjuvant (FCA) arthritis model) or nerve injury (chronic constriction injury model). We show that SK1, SK2, SK3 and IK1 are all expressed in DRG and spinal cord. Morphometric analysis revealed that SK1, SK2 and IK1 were preferentially localized to neurones having cell bodies <1000 microm2 (putative nociceptors)in DRG. Dual labeling immunocytochemistry showed that these ion channels co-localize with both CGRP and IB4, known markers of nociceptor sub-populations. SK2 was localized almost exclusively in the superficial laminae of the spinal cord dorsal horn, the region in which many sensory afferents terminate; the distribution of SK1 and IK1 was more widespread in spinal cord, although some preferential labeling within the dorsal horn was observed in the case of IK1. Here we show evidence for a distinctive pattern of expression for certain members of the calcium-activated potassium channel family in the rat DRG.
机译:小电导(SK)和中电导(IK)钙激活的钾离子通道是调节伤害性神经元兴奋性的候选离子通道。我们已经使用独特的肽指导的抗血清来描述这些离子通道的已知同工型在大鼠背根神经节(DRG)和脊髓中的免疫细胞化学分布。这些研究试图进一步表征大鼠中伤害性神经元亚群的表型以及可能的功能。另外,使用蛋白质印迹法,我们试图确定诱导炎症(弗氏完全佐剂(FCA)关节炎模型)或神经损伤(慢性收缩损伤模型)后感觉神经组织中SK和IK通道蛋白的表达水平。我们显示SK1,SK2,SK3和IK1均在DRG和脊髓中表达。形态计量学分析显示,在DRG中,SK1,SK2和IK1优先定位于细胞体<1000 microm2(假定伤害感受器)的神经元。双重标记免疫细胞化学显示,这些离子通道与CGRP和IB4(伤害感受器亚群的已知标记)共定位。 SK2几乎完全定位在脊髓背角的浅层,许多感觉传入终止于此。尽管在IK1中观察到了一些在背角内的优先标记,但SK1和IK1在脊髓中的分布更为广泛。在这里,我们显示了大鼠DRG中钙激活钾通道家族某些成员的独特表达模式的证据。

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