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Serotonin Transporter Polymorphism Mediates Vulnerability to Loss of Incentive Motivation Following Acute Tryptophan Depletion

机译:5-羟色胺转运蛋白多态性介导的脆弱色氨酸耗竭后失去动力的动机。

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摘要

The serotonin (5-HT) system is implicated in incentive motivational processes. The present study utilized the acute tryptophan depletion (ATD) procedure to investigate the effect of temporarily lowering 5-HT synthesis on motivation in healthy volunteers, stratifying the results by allelic variation at the serotonin transporter gene (5-HTTLPR). ATD resulted in a robust reduction in plasma tryptophan concentration. Consistent with a previous study, ATD attenuated motivationally speeded action on the Cued-Reinforcement Reaction Time task. The present investigation revealed that this effect was restricted to volunteers of the ss genotype, whereas ll volunteers exhibited intact motivationally speeded action following ATD (treatment × reinforcement probability × genotype interaction: F1,26 = 5.8, p = 0.024). Furthermore, tryptophan availability to the brain was correlated positively with motivationally speeded action following ATD in the ss genotype group (ρ13 = 0.71, p = 0.006), whereas this correlation was negative in the ll genotype group (ρ14 = −0.60, p = 0.023). This is the first study to suggest that allelic variation at the 5-HTTLPR mediates motivational responses to ATD in healthy volunteers. These data indicate that the s allele at the 5-HTTLPR may confer risk for depression via its effect on incentive motivational processing, and highlight the importance of genetic variation in determining individual responses to pharmacological treatments.
机译:血清素(5-HT)系统与激励动机过程有关。本研究利用急性色氨酸耗竭(ATD)程序研究了暂时降低5-HT合成对健康志愿者动机的影响,通过5-羟色胺转运蛋白基因(5-HTTLPR)的等位基因变异对结果进行分层。 ATD导致血浆色氨酸浓度大幅降低。与以前的研究一致,ATD减弱了对“暗示增强反应时间”任务的激励性动作。目前的研究表明,这种影响仅限于ss基因型的志愿者,而11名志愿者在ATD后表现出完整的动机性加速动作(治疗×强化概率×基因型相互作用:F1,26 = 5.8,p = 0.024)。此外,在ss基因型组中,脑中色氨酸的可利用性与ATD激发后的动机性行动呈正相关(ρ13= 0.71,p = 0.006),而在ll基因型组中,这种相关性为负(ρ14= -0.60,p = 0.023) )。这是第一项表明5-HTTLPR等位基因变异介导健康志愿者对ATD的激励反应的研究。这些数据表明5-HTTLPR上的s等位基因可能通过其对激励动机过程的影响而赋予患抑郁症的风险,并突显了遗传变异在确定对药物治疗的个体反应中的重要性。

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