Literature DB >> 22094432

Perception of a naturalistic stressor interacts with 5-HTTLPR/rs25531 genotype and gender to impact reward responsiveness.

Yuliya Nikolova1, Ryan Bogdan, Diego A Pizzagalli.   

Abstract

BACKGROUND: Stressful life experiences frequently precede the onset of major depression; however, the mechanisms that underlie this link are poorly understood. Importantly, some individuals are more susceptible to the depressogenic effects of stress than others. Carriers of the S or LG allele of the 5-HTTLPR/rs25531 polymorphisms (S' participants) have been found to be more prone to developing depression under stress relative to L or LA homozygotes (L' participants). Moreover, emerging evidence indicates that stress-induced anhedonia may be a mechanism underlying links between stress and depression. Given these findings, we hypothesized that exposure to a naturalistic stressor (school final examinations) would disrupt reward responsiveness (a key behavioral component of anhedonia), and that this effect would be strongest in S' participants.
METHODS: To objectively assess reward responsiveness, we administered a probabilistic reward task to 70 Bulgarian high school students over two sessions in the 6-month period preceding school finals. For each participant, the two sessions were designated as the 'stress' and 'control' conditions based on self-reported perceived stress.
RESULTS: A genotype×condition interaction emerged in males, with S' participants showing larger stress-related reduction in reward responsiveness relative to L' participants.
CONCLUSION: While in need of replication in a larger sample, our results indicate that stress associated with a real-life event is linked to reduced reward responsiveness, the susceptibility to which is modulated by 5-HTTLPR/rs25531 genotype. Although preliminary, these findings identify anhedonia as a promising mechanism linking 5-HTTLPR/rs25531 genotype and stress to depression.
Copyright © 2011 S. Karger AG, Basel.

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Year:  2011        PMID: 22094432      PMCID: PMC3238029          DOI: 10.1159/000329105

Source DB:  PubMed          Journal:  Neuropsychobiology        ISSN: 0302-282X            Impact factor:   2.328


  56 in total

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2.  Association of a triallelic serotonin transporter gene promoter region (5-HTTLPR) polymorphism with stressful life events and severity of depression.

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4.  A common polymorphism in the mineralocorticoid receptor modulates stress responsiveness.

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Review 5.  Stress, depression, and anhedonia: caveats concerning animal models.

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6.  Mental performance in old age dependent on cortisol and genetic variance in the mineralocorticoid and glucocorticoid receptors.

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Review 8.  Chronic mild stress (CMS) revisited: consistency and behavioural-neurobiological concordance in the effects of CMS.

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10.  Increased perceived stress is associated with blunted hedonic capacity: potential implications for depression research.

Authors:  Diego A Pizzagalli; Ryan Bogdan; Kyle G Ratner; Allison L Jahn
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  19 in total

Review 1.  Sex differences modulating serotonergic polymorphisms implicated in the mechanistic pathways of risk for depression and related disorders.

Authors:  LeeAnn M Perry; Andrea N Goldstein-Piekarski; Leanne M Williams
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2.  Corticotropin-releasing hormone receptor type 1 (CRHR1) genetic variation and stress interact to influence reward learning.

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3.  Evidence of a diurnal rhythm in implicit reward learning.

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Review 4.  Peril and pleasure: an rdoc-inspired examination of threat responses and reward processing in anxiety and depression.

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5.  Striatal Hypersensitivity During Stress in Remitted Individuals with Recurrent Depression.

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Review 6.  Anhedonia: a concept analysis.

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7.  Social defeat disrupts reward learning and potentiates striatal nociceptin/orphanin FQ mRNA in rats.

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Review 8.  Depression, stress, and anhedonia: toward a synthesis and integrated model.

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