首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Increased protein levels of serotonin transporter in frontal cortex of patients with Down syndrome.
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Increased protein levels of serotonin transporter in frontal cortex of patients with Down syndrome.

机译:唐氏综合症患者额叶皮质5-羟色胺转运蛋白的蛋白水平升高。

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Serotonin transporters (SERTs) are presynaptic proteins specialized for the clearance of serotonin from the synaptic cleft. A large body of evidence exists on altered platelet serotonin uptake and metabolism in Down syndrome (DS). Besides, dysregulation of SERTs expression have been reported in various complex behavioural traits and disorders including, neurodegenerative disorders. This prompted us to investigate SERT protein levels in adult brain specimens. Western blot analyses were performed in frontal cortex and cerebellum of aged controls and patients with DS and Alzheimer's disease (AD). The result revealed that frontal cortex SERT was significantly increased (P<0.05) in DS, whereas in AD it was comparable to controls. In cerebellum, no significant difference was observed among the study populations. A remarkable difference was noted when SERT was normalized vs. neuron specific enolase (NSE), a neuronal marker. The increase in SERT/NSE was highly significant (P<0.01) in DS frontal cortex compared to controls. Neither AD frontal cortex nor DS and AD cerebellum did show any significant difference. These findings indicate that a region specific alteration in SERT expression may exist in DS with AD-like pathology. As little is known about the status of serotenergic synaptic markers in DS brain, the findings may contribute to an effort made to delineate the underlying causes of serotonergic dysfunction in DS and the quest for therapeutic strategies. The study also suggest caution should be taken in applying data obtained from DS to model AD biochemical defects.
机译:血清素转运蛋白(SERTs)是突触前蛋白,专门用于从突触间隙清除5-羟色胺。在唐氏综合症(DS)中,血小板血清素摄取和代谢改变的大量证据。此外,已经报道了在多种复杂的行为特征和病症中包括神经变性疾病的SERT表达的失调。这促使我们研究成人脑标本中的SERT蛋白水平。在老年对照以及DS和阿尔茨海默氏病(AD)患者的额叶皮层和小脑中进行蛋白质印迹分析。结果表明,额叶皮层SERT在DS中显着增加(P <0.05),而在AD中则与对照组相当。在小脑中,研究人群之间没有观察到显着差异。当将SERT标准化与神经元特异性神经元特异性烯醇化酶(NSE)相比时,注意到了显着差异。与对照组相比,DS额叶皮层中SERT / NSE的增加非常显着(P <0.01)。 AD额叶皮质和DS及AD小脑均未显示任何显着差异。这些发现表明,具有AD样病理的DS中可能存在SERT表达的区域特异性改变。关于DS脑中的血清素能突触标记物的状态知之甚少,这些发现可能有助于描述DS中血清素能功能障碍的潜在原因以及寻求治疗策略。该研究还建议在将从DS获得的数据应用于AD生化缺陷模型时应谨慎。

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