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催产素受体(OXTR)基因与奖励性中脑边缘反应之间的关系。

Association between the oxytocin receptor (OXTR) gene and mesolimbic responses to rewards.

机构信息

Department of Psychology, University of North Carolina, CB#3270, Davie Hall, UNC-CH, Chapel Hill, NC 27599, USA.

出版信息

Mol Autism. 2014 Jan 31;5(1):7. doi: 10.1186/2040-2392-5-7.

Abstract

BACKGROUND

There has been significant progress in identifying genes that confer risk for autism spectrum disorders (ASDs). However, the heterogeneity of symptom presentation in ASDs impedes the detection of ASD risk genes. One approach to understanding genetic influences on ASD symptom expression is to evaluate relations between variants of ASD candidate genes and neural endophenotypes in unaffected samples. Allelic variations in the oxytocin receptor (OXTR) gene confer small but significant risk for ASDs for which the underlying mechanisms may involve associations between variability in oxytocin signaling pathways and neural response to rewards. The purpose of this preliminary study was to investigate the influence of allelic variability in the OXTR gene on neural responses to monetary rewards in healthy adults using functional magnetic resonance imaging (fMRI).

METHODS

The moderating effects of three single nucleotide polymorphisms (SNPs) (rs1042778, rs2268493 and rs237887) of the OXTR gene on mesolimbic responses to rewards were evaluated using a monetary incentive delay fMRI task.

RESULTS

T homozygotes of the rs2268493 SNP demonstrated relatively decreased activation in mesolimbic reward circuitry (including the nucleus accumbens, amygdala, insula, thalamus and prefrontal cortical regions) during the anticipation of rewards but not during the outcome phase of the task. Allelic variation of the rs1042778 and rs237887 SNPs did not moderate mesolimbic activation during either reward anticipation or outcomes.

CONCLUSIONS

This preliminary study suggests that the OXTR SNP rs2268493, which has been previously identified as an ASD risk gene, moderates mesolimbic responses during reward anticipation. Given previous findings of decreased mesolimbic activation during reward anticipation in ASD, the present results suggest that OXTR may confer ASD risk via influences on the neural systems that support reward anticipation.

摘要

背景

在鉴定与自闭症谱系障碍(ASD)相关的风险基因方面已经取得了重大进展。然而,ASD 的症状表现存在异质性,这阻碍了 ASD 风险基因的检测。了解遗传对 ASD 症状表现影响的一种方法是评估 ASD 候选基因的变异与未受影响样本中的神经内表型之间的关系。催产素受体(OXTR)基因的等位基因变异赋予了较小但显著的 ASD 风险,其潜在机制可能涉及催产素信号通路的变异性与对奖励的神经反应之间的关联。本初步研究旨在使用功能磁共振成像(fMRI)研究 OXTR 基因的等位基因变异性对健康成年人对金钱奖励的神经反应的影响。

方法

使用货币奖励延迟 fMRI 任务,评估 OXTR 基因的三个单核苷酸多态性(SNP)(rs1042778、rs2268493 和 rs237887)的等位基因变异对奖赏的中脑边缘反应的调节作用。

结果

rs2268493 SNP 的 T 纯合子在奖励预期期间,而不是在任务结果阶段,中脑边缘奖赏回路(包括伏隔核、杏仁核、岛叶、丘脑和前额叶皮质区域)的激活相对降低。rs1042778 和 rs237887 SNP 的等位基因变异在奖励预期或结果期间均不能调节中脑边缘激活。

结论

本初步研究表明,先前被确定为 ASD 风险基因的 OXTR SNP rs2268493 调节奖励预期期间的中脑边缘反应。鉴于 ASD 中奖励预期期间中脑边缘激活减少的先前发现,本研究结果表明,OXTR 可能通过对支持奖励预期的神经系统的影响来赋予 ASD 风险。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/306e/3922109/44646d6f030e/2040-2392-5-7-1.jpg

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