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神经发育障碍中血清素受体的调节:聚焦于5-羟色胺7受体

Modulation of Serotonin Receptors in Neurodevelopmental Disorders: Focus on 5-HT7 Receptor.

作者信息

Lee Jieon, Avramets Diana, Jeon Byungsun, Choo Hyunah

机构信息

Brain Science Institute, Korea Institute of Science and Technology, Seongbuk-gu, Seoul 02792, Korea.

Division of Bio-Medical Science & Technology, KIST School, Korea University of Science and Technology, Seoul 02792, Korea.

出版信息

Molecules. 2021 Jun 2;26(11):3348. doi: 10.3390/molecules26113348.

Abstract

Since neurodevelopmental disorders (NDDs) influence more than 3% of children worldwide, there has been intense investigation to understand the etiology of disorders and develop treatments. Although there are drugs such as aripiprazole, risperidone, and lurasidone, these medications are not cures for the disorders and can only help people feel better or alleviate their symptoms. Thus, it is required to discover therapeutic targets in order to find the ultimate treatments of neurodevelopmental disorders. It is suggested that abnormal neuronal morphology in the neurodevelopment process is a main cause of NDDs, in which the serotonergic system is emerging as playing a crucial role. From this point of view, we noticed the correlation between serotonin receptor subtype 7 (5-HTR) and NDDs including autism spectrum disorder (ASD), fragile X syndrome (FXS), and Rett syndrome (RTT). 5-HTR modulators improved altered behaviors in animal models and also affected neuronal morphology via the 5-HTR/G signaling pathway. Through the investigation of recent studies, it is suggested that 5-HTR could be a potential therapeutic target for the treatment of NDDs.

摘要

由于神经发育障碍(NDDs)影响着全球超过3%的儿童,人们对了解这些疾病的病因并开发治疗方法进行了深入研究。虽然有阿立哌唑、利培酮和鲁拉西酮等药物,但这些药物并不能治愈这些疾病,只能帮助人们感觉更好或缓解症状。因此,需要发现治疗靶点以找到神经发育障碍的最终治疗方法。有人认为神经发育过程中异常的神经元形态是NDDs的主要原因,其中血清素能系统正发挥着关键作用。从这一角度来看,我们注意到血清素受体亚型7(5-HTR)与包括自闭症谱系障碍(ASD)、脆性X综合征(FXS)和雷特综合征(RTT)在内的NDDs之间的关联。5-HTR调节剂改善了动物模型中改变的行为,并且还通过5-HTR/G信号通路影响神经元形态。通过对近期研究的调查,表明5-HTR可能是治疗NDDs的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96d4/8199608/7e393b46efdf/molecules-26-03348-g001.jpg

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