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MicroRNA-328a regulates water maze performance in PTZ-kindled rats

机译:MicroRNA-328a调节PTZ点燃的大鼠的水迷宫性能

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The down-regulation of microRNA-328a (miR-328a) in pentylenetetrazole (PTZ)-kindled rats with memory impairment was demonstrated in our previous study, while any contribution of miR-328a to cognitive dysfunction of PTZ-kindled rats remains unknown. In this study we have investigated the effect and the underlying mechanism of miR-328a on the cognitive function in PTZ-kindled rats. 48 SD male rats were divided into 4 groups as follows: a PTZ kindled group, a miR-328a antagomir group, an antagomir-control group, and a sham group (n = 12 for each). All rats except those from the sham group were treated with PTZ 14 times at intervals of 48 h to establish the temporal lobe epilepsy (TLE) models, and miR-328a antagomir was given to the antagomir group as a treatment by lateral-ventricle injection the day after the first injection of PTZ. Morris water maze (MWM) test was performed to assay their learning and memory abilities. The down-regulation of miR-328a in the PTZ group was confirmed using RT-qPCR and the expression of miR-328a was diminished after antagomir treatment (P < 0.05). In the probe test of water maze, the time and distance of the PTZ group were both shorter than those of the sham group (P < 0.05), and those of the antagomir-control group were both longer than those of the antagomir group (P < 0.05). In addition, we found that with the down-regulation of miR-328a, the levels of Beta-site APP-cleaving enzyme (BACE), which is a bioinformatics-predicted target of miR-328a, were up-regulated. These findings suggest that miR-328a may play a role in memory dysfunction in PTZ-kindled rats by regulating the BACE levels and this links the PTZ model with Alzheimer's disease. (C) 2016 The Authors. Published by Elsevier Inc.
机译:在我们先前的研究中,证实了戊四氮(PTZ)致记忆障碍的大鼠中microRNA-328a(miR-328a)的下调,而miR-328a对PTZ致大鼠认知功能障碍的任何贡献仍然未知。在这项研究中,我们研究了miR-328a对PTZ点燃的大鼠认知功能的影响及其潜在机制。将48只SD雄性大鼠分为4组:PTZ点燃组,miR-328a antagomir组,antagomir对照组和假组(每组n = 12)。除假手术组外的所有大鼠均在48 h间隔内进行PTZ治疗14次,建立颞叶癫痫(TLE)模型,并将miR-328a antagomir给予antagomir组,通过侧脑室注射治疗。第一次注射PTZ后的第二天。进行莫里斯水迷宫(MWM)测试以测定其学习和记忆能力。用RT-qPCR证实了PTZ组中miR-328a的下调,并且在antagomir处理后miR-328a的表达降低了(P <0.05)。在水迷宫的探针测试中,PTZ组的时间和距离均比假手术组短(P <0.05),而antagomir-对照组的时间和距离均长于antagomir组(P <0.05)。此外,我们发现随着miR-328a的下调,β-位APP裂解酶(BACE)的水平也被上调,Beta位点是生物信息学预测的miR-328a靶标。这些发现表明,miR-328a可能通过调节BACE水平在PTZ点燃的大鼠的记忆功能障碍中发挥作用,这将PTZ模型与阿尔茨海默氏病联系起来。 (C)2016作者。由Elsevier Inc.发布

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