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Kv7.2 subunit-containing M-type potassium channels in the lateral habenula are involved in the regulation of working memory in parkinsonian rats

机译:kv7.2亚单位的亚单位的M型钾通道在横向湿地中参与了帕金森大鼠工作记忆的调节

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Although the lateral habenula (LHb) is involved in the regulation of multiple brain functions and this region expresses abundant M-type potassium channel (M-channel) subunits Kv7.2 and Kv7.3, the role of M-channels in regulating working memory is unclear, particularly in Parkinson's disease (PD). Here we tested the effects of activation and blockade of LHb M-channels on working memory by the T-maze rewarded alternation test in rats with unilateral 6-hydroxydopamine lesions of the substantia nigra compacta (SNc). The SNc lesion induced working memory impairment, increased the firing rate of LHb neurons, decreased dopamine (DA) level in the ventral medial prefrontal cortex (vmPFC) and reduced the expression of Kv7.2 subunit in the LHb. Intra-LHb injection of M-channel activator retigabine induced enhancement of working memory in SNc sham-lesioned and SNc-lesioned rats; conversely, the injection of M-channel blocker XE-991 impaired working memory in the two groups of rats. However, doses producing significant effects in SNc-lesioned rats were higher than those in SNc sham-lesioned rats. Further, intra-LHb injection of retigabine decreased the firing rate of LHb neurons and increased release of DA and serotonin (5-HT) in the vmPFC, while XE-991 increased the firing rate and decreased DA and 5-HT release in the two groups of rats. Compared with SNc sham-lesioned rats, the duration of M-channel activation and blockade action on the firing rate of the neurons and release of DA and 5-HT was significantly shortened in SNc-lesioned rats, which was consistent with reduced expression of Kv7.2 subunit in the LHb after lesioning the SNc. Collectively, these findings suggest involvement of LHb Kv7.2 subunit-containing M-channels in working memory impairment in SNc-lesioned rats, and that enhanced or impaired working memory after activation or blockade of M-channels in the LHb is related to the changes in the firing activity of LHb neurons and DA and 5-HT release in the vmPFC.
机译:虽然横向Habenula(LHB)参与了多脑功能的调节,但该区域表达了丰富的M型钾通道(M沟道)亚基KV7.2和KV7.3,M-Chancels在调节工作记忆中的作用尚不清楚,特别是在帕金森病(PD)中。在这里,我们通过在大鼠内部6-羟基多胺病变(SNC)的大鼠中,通过T-Maze奖励交替试验测试了激活和阻断LHB M-通道的影响。 SNC病变诱导的工作记忆障碍,增加了LHB神经元的烧制率,降低了腹侧前额叶皮质(VMPFC)中的多巴胺(DA)水平,并降低了LHB中KV7.2亚基的表达。 LHB内部注射M沟道活化剂重载诱导的SNC假损伤和SNC损伤大鼠工作记忆的增强;相反,在两组大鼠中注射M沟道阻滞剂XE-991受损的工作记忆。然而,在SNC损伤大鼠中产生显着影响的剂量高于SNC假损伤大鼠的剂量。此外,LHB内注射克重扣降低了LHB神经元的烧制率,并在VMPFC中增加了DA和血清素(5-HT)的释放,而XE-991增加了烧制率并降低了两者和5-HT释放大鼠群体。与SNC假损伤的大鼠相比,在SNC损伤的大鼠中,M沟道激活和对DA和5-HT释放的烧制率的阻断作用显着缩短,这与kV7的表达相一致.2在SNC损伤后LHB中的亚基。这些研究结果表明,LHB KV7.2亚单位的M-通道在SNC损伤大鼠中的工作记忆损伤中涉及,并且在LHB中激活或阻断M-Chancels后增强或受损的工作记忆与变化有关在VMPFC中的LHB神经元和DA和5-HT释放的烧制活性。

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