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血清素转运体相关启动子区域三基因座功能多态性对人脑中血清素转运体表达的影响。

Effect of a triallelic functional polymorphism of the serotonin-transporter-linked promoter region on expression of serotonin transporter in the human brain.

作者信息

Parsey Ramin V, Hastings Ramin S, Oquendo Maria A, Hu Xianzhang, Goldman David, Huang Yung-yu, Simpson Norman, Arcement Julie, Huang Yiyun, Ogden R Todd, Van Heertum Ronald L, Arango Victoria, Mann J John

机构信息

Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York, USA.

出版信息

Am J Psychiatry. 2006 Jan;163(1):48-51. doi: 10.1176/appi.ajp.163.1.48.

Abstract

OBJECTIVE

The authors examined effects of a triallelic functional polymorphism of the human serotonin-transporter-linked promoter region (5-HTTLPR) on in vivo expression of serotonin transporter in the brain in healthy volunteers and subjects with major depressive disorder.

METHOD

Twenty-five medication-free subjects with DSM-IV major depressive disorder during a major depressive episode and 42 healthy volunteers were clinically evaluated and genotyped. Serotonin transporter binding potential (f(1)B(max)/K(d)) was determined by using positron emission tomography with the radiotracer [(11)C]McN 5652 and metabolite-corrected arterial input functions.

RESULTS

There was no difference in serotonin transporter binding potential by genotype in healthy volunteers or in subjects with major depressive disorder. Allelic frequencies did not differ between subjects with major depressive disorder and healthy volunteers.

CONCLUSIONS

Associations of the 5-HTTLPR polymorphism to clinical phenotypes appear to be due to developmental effects of 5-HTTLPR on expression and not due to its direct effect on serotonin transporter binding in adulthood.

摘要

目的

作者研究了人类血清素转运体相关启动子区域(5-HTTLPR)的三基因座功能多态性对健康志愿者和重度抑郁症患者大脑中血清素转运体体内表达的影响。

方法

对25名处于重度抑郁发作期且未服用药物的DSM-IV重度抑郁症患者和42名健康志愿者进行临床评估和基因分型。使用放射性示踪剂[(11)C]McN 5652和代谢物校正动脉输入函数的正电子发射断层扫描来测定血清素转运体结合潜能(f(1)B(max)/K(d))。

结果

健康志愿者或重度抑郁症患者中,血清素转运体结合潜能在不同基因型之间没有差异。重度抑郁症患者和健康志愿者的等位基因频率没有差异。

结论

5-HTTLPR多态性与临床表型的关联似乎是由于5-HTTLPR对表达的发育影响,而非其对成年期血清素转运体结合的直接影响。

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