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The role of miRNA in the pain mechanisms

The role of miRNA in the pain mechanisms
miRNA在疼痛机制中的作用
批准号:
20390417
负责人:
HAGIHIRA Satoshi
金额:
$12.65万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2008
资助国家:
日本
项目状态:
已结题
起止时间:
2008 至 2010

项目摘要

项目成果

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中文摘要
翻译
在目前的研究中,我们研究了多种mirna的功能,重点关注那些被认为是GABAA α 5受体(Gabra5)调控的潜在靶点。该方法鉴定了六个候选的mirna,它们是Gabra5调控的候选mirna (miR 598-3p、miR541、miR378、miR219-2-3p、miR223和miR346)。荧光素酶测定证实,这6个mirna靶向Gabra5中的特定序列。接下来,我们检查了这些miRNAs是否在蛋白水平上降低了Gabra5的表达。我们发现只有miR378和miR541负调控海马神经元中的Gabra5蛋白。Gabra5在认知和记忆中起着重要作用。通过增加Gabra5的表达水平,我们可能能够改善患有认知问题和记忆功能障碍的阿尔茨海默病患者的症状。miR378和miR541抑制剂是这种推测的新疗法的潜在靶点。
英文摘要
In the current study, we investigated the function of multiple miRNAs, focusing on those that are considered potential targets for GABAA alpha 5 receptor (Gabra5) regulation.The in silico approach identified six miRNAs that were candidates for Gabra5 regulation (miR 598-3p, miR541, miR378, miR219-2-3p, miR223, and miR346). Luciferase assays confirmed that the six miRNAs targeted specific sequences within Gabra5. We next examined whether these miRNAs reduced Gabra5 expression at the protein level. We found that only miR378 and miR541 negatively regulated Gabra5 protein in hippocampal neurons.Gabra5 plays an important role in cognition and memory. By increasing the expression level of Gabra5, we might be able to ameliorate the symptoms of patients with Alzheimer's disease, who suffer from cognitive problems and memory dysfunction. Inhibitors of miR378 and miR541 are potential targets for this putative new therapy.
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The snoRNA RBII-52 regulates alternative splicing of serotonin 2C receptor in the rat oro-facial neuropathic paimodel.
snoRNA RBII-52 调节大鼠口面部神经病变模型中血清素 2C 受体的选择性剪接。
DOI: --
发表时间: 2009
期刊:
影响因子: --
作者: [Aya Nakae, Kunihiro Nakai, Tatsuya Tanaka, Mari Yoshida, Akiko Mikam, Masaki Takashina, Satoshi Hagihira, Masahiko Shibata, Koichi Ueda, Takashi ashimo]
通讯作者: Takashi ashimo
The role of snoRNA in a rat model of oro-facial neuropathic pain.
snoRNA 在口面部神经病理性疼痛大鼠模型中的作用。
DOI: --
发表时间: 2009
期刊:
影响因子: --
作者: [Aya Nakae, Kunihiro Nakai, Tatsuya Tanaka, Satoshi Hagihira, Takashi Mashimo]
通讯作者: Takashi Mashimo
Serotonin2C receptor mRNA editing in neuropathic pain model.
神经病理性疼痛模型中 5-羟色胺2C 受体 mRNA 编辑。
DOI: --
发表时间: 2007
期刊: Neuroscience Research 60(2)
影响因子: --
作者: [Aya Nakae, et. al.]
通讯作者: et. al.
PregnaDoes Not Enhance Volatile Anestheic Sensitivity on the Brain : An Electroencephalographic Aalysis Study.
怀孕不会增强大脑对挥发性麻醉剂的敏感性:脑电图分析研究。
DOI: --
发表时间: 2010
期刊: Anesthesiology 113(3)
影响因子: --
作者: [Ueyama H, Hagihira S, Takashina M, Nakae A, Mashi T.]
通讯作者: Mashi T.
29
    Pain chronisity and attention control
    • 批准号:
      23592287
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.16万
    • 财政年份:
      2011
    • 负责人:
      HAGIHIRA Satoshi
    • 依托单位:
    The mechanism of neuron pathic pain analyzed by DNA microarray.
    • 批准号:
      15390473
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $9.09万
    • 财政年份:
      2003
    • 负责人:
      HAGIHIRA Satoshi
    • 依托单位:
    海外基金