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首页> 外文期刊>Philosophical Transactions of the Royal Society of London, Series B. Biological Sciences >Transcriptional regulation of the 5-HT 1A receptor: Implications for mental illness (Review)
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Transcriptional regulation of the 5-HT 1A receptor: Implications for mental illness (Review)

机译:5-HT 1A受体的转录调控:对精神疾病的影响(综述)

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The serotonin-1A (5-HT _(1A)) receptor is an abundant post-synaptic 5-HT receptor (heteroreceptor) implicated in regulation of mood, emotion and stress responses and is the major somatodendritic autoreceptor that negatively regulates 5-HT neuronal activity. Based on animal models, an integrated model for opposing roles of pre- and post-synaptic 5-HT _(1A) receptors in anxiety and depression phenotypes and response to antidepressants is proposed. Understanding differential transcriptional regulation of pre- versus post-synaptic 5-HT _(1A) receptors could provide better tools for their selective regulation. This review examines the transcription factors that regulate brain region-specific basal and stress-induced expression of the 5-HT _(1A) receptor gene (Htr1a). A functional polymorphism, rs6295 in the Htr1a promoter region, blocks the function of specific repressors Hes1, Hes5 and Deaf1, resulting in increased 5-HT _(1A) autoreceptor expression in animal models and humans. Its association with altered 5-HT _(1A) expression, depression, anxiety and antidepressant response are related to genotype frequency in different populations, sample homogeneity, disease outcome measures and severity. Preliminary evidence from gene × environment studies suggests the potential for synergistic interaction of stress-mediated repression of 5-HT _(1A) heteroreceptors, and rs6295-induced upregulation of 5-HT _(1A) autoreceptors. Targeted therapeutics to inhibit 5-HT _(1A)autoreceptor expression and induce 5-HT _(1A) heteroreceptor expression may ameliorate treatment of anxiety and major depression.
机译:血清素1A(5-HT _(1A))受体是一种丰富的突触后5-HT受体(异源受体),涉及情绪,情绪和压力反应的调节,并且是主要的体树突触自体受体,对5-HT神经元产生负调节作用。活动。基于动物模型,提出了一个综合模型,针对突触前后5-HT_(1A)受体在焦虑和抑郁表型以及对抗抑郁药的反应中的相反作用。了解突触前5-HT_(1A)受体的差异转录调控可能为它们的选择性调控提供更好的工具。这篇评论检查了转录因子,调节脑区域特定的基础和应激诱导的5-HT _(1A)受体基因(Htr1a)的表达。 Htr1a启动子区域中的功能性多态性rs6295阻断了特定阻遏物Hes1,Hes5和Deaf1的功能,导致动物模型和人类体内5-HT _(1A)自受体表达增加。它与5-HT _(1A)表达改变,抑郁,焦虑和抗抑郁反应的相关性与不同人群的基因型频率,样本均一性,疾病结果指标和严重程度有关。来自基因×环境研究的初步证据表明,应激介导的5-HT _(1A)异源受体抑制和rs6295诱导的5-HT _(1A)自体受体上调可能具有协同相互作用的潜力。抑制5-HT _(1A)自体受体表达并诱导5-HT _(1A)异体受体表达的靶向疗法可改善焦虑症和重度抑郁症的治疗。

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