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血清素转运体相关启动子区域多态性与精神分裂症或人类海马体中血清素转运体密度之间无关联。

No association between the serotonin transporter-linked promoter region polymorphism and either schizophrenia or density of the serotonin transporter in human hippocampus.

作者信息

Naylor L, Dean B, Pereira A, Mackinnon A, Kouzmenko A, Copolov D

机构信息

Rebecca L. Cooper Research Laboratories, Molecular Schizophrenia Division, Mental Health Research Institute of Victoria, Parkville, Australia.

出版信息

Mol Med. 1998 Oct;4(10):671-4.

Abstract

BACKGROUND

Allelic association case-control analysis of a deletion/insertion polymorphism in the serotonin transporter-linked polymorphic region (5-HTTLPR) has suggested associations with unipolar disorder, bipolar disorder, depression, and Alzheimer's disease. Moreover, the heterozygous long form of the 5-HTTLPR has been associated with increased levels of mRNA for the serotonin transporter (5-HTT) and increased serotonin uptake in lymphoblastic cell lines. This study attempts to determine whether there is an association between 5-HTTLPR genotype and schizophrenia or the binding of [3H]paroxetine to the human hippocampal 5-HTT.

MATERIALS AND METHODS

DNA from the cerebellum from 58 schizophrenic and 62 control subjects was used to genotype the 5-HTTLPR. In addition, the relationship between 5-HTTLPR genotype and the affinity and density of [3H]paroxetine binding to the hippocampal 5-HTT was assessed.

RESULTS

There were no associations between 5-HTTLPR allotype or genotype and/or the parameters of [3H]paroxetine binding to the hippocampal 5-HTT.

CONCLUSIONS

Our data suggest that 5-HTTLPR genotype neither confers an increased susceptibility for schizophrenia nor dictates the expression of the 5-HTT in the human hippocampus.

摘要

背景

对5-羟色胺转运体相关多态性区域(5-HTTLPR)中的缺失/插入多态性进行等位基因关联病例对照分析,结果提示其与单相情感障碍、双相情感障碍、抑郁症及阿尔茨海默病有关。此外,5-HTTLPR的杂合长型与5-羟色胺转运体(5-HTT)的mRNA水平升高以及淋巴细胞系中5-羟色胺摄取增加有关。本研究旨在确定5-HTTLPR基因型与精神分裂症之间是否存在关联,以及[3H]帕罗西汀与人海马5-HTT的结合情况。

材料与方法

采用58例精神分裂症患者及62例对照者小脑的DNA对5-HTTLPR进行基因分型。此外,评估了5-HTTLPR基因型与[3H]帕罗西汀结合海马5-HTT的亲和力及密度之间的关系。

结果

5-HTTLPR别型或基因型与[3H]帕罗西汀结合海马5-HTT的参数之间无关联。

结论

我们的数据表明,5-HTTLPR基因型既不会增加精神分裂症的易感性,也不会决定人海马中5-HTT 的表达。

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