首页> 外文期刊>Neuropeptides: An International Journal >Altered expression of neuropeptide Y, Y1 and Y2 receptors, but not Y5 receptor, within hippocampus and temporal lobe cortex of tremor rats.
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Altered expression of neuropeptide Y, Y1 and Y2 receptors, but not Y5 receptor, within hippocampus and temporal lobe cortex of tremor rats.

机译:震颤大鼠海马和颞叶皮层神经肽Y,Y1和Y2受体的表达改变,但不改变Y5受体的表达。

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As an endogenous inhibitor of glutamate-mediated synaptic transmission in mammalian central nervous system, neuropeptide Y (NPY) plays a crucial role in regulating homeostasis of neuron excitability. Loss of balance between excitatory and inhibitory neurotransmission is thought to be a chief mechanism of epileptogenesis. The abnormal expression of NPY and its receptors observed following seizures have been demonstrated to be related to the production of epilepsy. The tremor rat (TRM) is a hereditary epileptic animal model. So far, there is no report concerning whether NPY and its receptors may be involved in TRM pathogenesis. In this study, we focused on the expression of NPY and its three receptor subtypes: Y1R, Y2R and Y5R in the TRM brain. We first found the expression of NPY in TRM hippocampus and temporal lobe cortex was increased compared with control (Wistar) rats. The mRNA and protein expression of Y1R was down-regulated in hippocampus but up-regulated in temporal lobe cortex, whereas Y2R expression was significantly increased in both areas. There was no significant change of Y5R expression in either area. The immunohistochemistry data showed that Y1R, Y2R, Y5R were present throughout CA1, CA3, dentate gyrus (DG) and the entorhinal cortex which is included in the temporal lobe cortex of TRM. In conclusion, our results showed the altered expression of NPY, Y1R and Y2R but not Y5R in hippocampus and temporal lobe cortex of TRM brain. This abnormal expression may be associated with the generation of epileptiform activity and provide a candidate target for treatment of genetic epilepsy.
机译:作为谷氨酸介导的突触传递在哺乳动物中枢神经系统中的内源性抑制剂,神经肽Y(NPY)在调节神经元兴奋性的稳态中起着至关重要的作用。兴奋性和抑制性神经传递之间失去平衡被认为是癫痫发生的主要机制。癫痫发作后观察到的NPY及其受体的异常表达已证明与癫痫的发生有关。震颤大鼠(TRM)是遗传性癫痫动物模型。迄今为止,尚无关于NPY及其受体是否可能参与TRM发病机制的报道。在这项研究中,我们专注于TRM脑中NPY及其三种受体亚型:Y1R,Y2R和Y5R的表达。我们首先发现,与对照组(Wistar)大鼠相比,NPY在TRM海马和颞叶皮层中的表达增加。在海马中,Y1R的mRNA和蛋白表达下调,但在颞叶皮质中上调,而在两个区域中,Y2R的表达均显着增加。在这两个区域中,Y5R表达均无显着变化。免疫组织化学数据显示,Y1R,Y2R,Y5R存在于TRM颞叶皮层中的CA1,CA3,齿状回(DG)和内嗅皮层中。总之,我们的结果表明,TRM脑海马和颞叶皮层中NPY,Y1R和Y2R的表达发生了变化,而Y5R没有发生变化。这种异常表达可能与癫痫样活动的产生有关,并提供了治疗遗传性癫痫的候选靶标。

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