Differential Effects of 5-HTTLPR Genotypes on Inhibition of Negative Emotional Information Following Acute Stress Exposure and Tryptophan Challenge
Differential Effects of 5-HTTLPR Genotypes on Inhibition of Negative Emotional Information Following Acute Stress Exposure and Tryptophan Challenge
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5-HTTLPR 基因型对急性应激暴露和色氨酸挑战后负面情绪信息抑制的差异作用
DOI:
10.1038/npp.2010.221
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发表时间:
2011
影响因子:
7.6
通讯作者:
R. Raedt
中科院分区:
文献类型:
--
作者:
C. Markus;R. Raedt
Previous data suggest that a polymorphism at the serotonin (5-HT) transporter gene (5-HTTLPR) may influence stress resilience and stress-related depression symptoms due to interactions between brain 5-HT dysfunction and stress exposure. Although attentional bias for emotional information has been reliably observed in depression, the interaction between 5-HT transporter-linked promoter region (5-HTTLPR), brain 5-HT vulnerability, and acute stress on affective information processing has not yet been investigated. This study examines the effects of tryptophan (TRP) augmentation (indicating 5-HT manipulation) on inhibition of negative emotional information under stress in mainly female S′/S′- vs L′/L′-allele carriers. A total of 15 female homozygotic short-allele 5-HTTLPR (S′/S′=S/S, S/LG, LG/LG) and 13 female homozygotic long-allele 5-HTTLPR (L′/L′=LA/LA) subjects were tested for mood and inhibition of emotional information in a double-blind, placebo-controlled design before and after stress exposure following TRP manipulation. Stress exposure significantly impaired inhibition of negative affective information only in S′/S′ carriers, whereas L′/L′ carriers even showed increased inhibition of negative information. The S′/S′ allele 5-HTTLPR genotype increases cognitive-attentional bias for negative emotional information under acute stress. As this bias is an important component of depression, this may be a mediating mechanism making S′/S′-allele carriers more vulnerability for stress-induced depression symptoms. Moreover, current data suggest that L′/L′-allele genotypes are more resilient, even increasing cognitive emotional (inhibitory) control after stress.
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影响因子:
120.7
作者:
Risch, Neil;Herrell, Richard;Lehner, Thomas;Liang, Kung-Yee;Eaves, Lindon;Hoh, Josephine;Griem, Andrea;Kovacs, Maria;Ott, Jurg;Merikangas, Kathleen Ries
通讯作者:
Merikangas, Kathleen Ries
DOI:
10.1176/ajp.2006.163.9.1588
发表时间:
2006-09
期刊:
The American journal of psychiatry
影响因子:
--
作者:
G. Zalsman;Yung-yu Huang;M. Oquendo;A. Burke;Xian-zhang Hu;D. Brent;S. Ellis;D. Goldman;J. Mann-J
通讯作者:
G. Zalsman;Yung-yu Huang;M. Oquendo;A. Burke;Xian-zhang Hu;D. Brent;S. Ellis;D. Goldman;J. Mann-J
影响因子:
--
作者:
Delgado,PL;Miller,HL;Salomon,RM;Licinio,J;Heninger,GR;Gelenberg,AJ;Charney,DS
通讯作者:
Charney,DS
影响因子:
--
作者:
Delgado,PL;Charney,DS;Price,LH;Aghajanian,GK;Landis,H;Heninger,GR
通讯作者:
Heninger,GR
DOI:
10.1073/pnas.94.10.5308
发表时间:
1997-05-13
影响因子:
11.1
作者:
Nishizawa, S;Benkelfat, C;Diksic, M
通讯作者:
Diksic, M