scholarly journals Neuroticism and reward-related ventral striatum activity: Probing vulnerability to stress-related depression.

2021 ◽  
Vol 130 (3) ◽  
pp. 223-235
Author(s):  
Erin Bondy ◽  
David A. A. Baranger ◽  
Jared Balbona ◽  
Kendall Sputo ◽  
Sarah E. Paul ◽  
...  
2020 ◽  
Author(s):  
Erin Bondy ◽  
David A Baranger ◽  
Jared V. Balbona ◽  
Kendall Sputo ◽  
Sarah Emily Paul ◽  
...  

Background: Elevated neuroticism may confer vulnerability to the depressogenic effects of stressful life events (SLEs). Vulnerability to stress-related disruption of neural reward processing is a promising neural mechanism undergirding links between stress and depression. Methods: Data came from 2 studies: the St. Louis Personality and Aging Network (SPAN) study and the Duke Neurogenetics Study (DNS). In SPAN, we used longitudinal self-reported data from older adults (n=971) to examine whether neuroticism moderates the association between recent stressful life events and subsequent depressive symptoms. In the DNS, we tested whether this interaction is present among young adult college students (n=1,343), and further whether neuroticism moderates the association between SLEs and reward-related ventral striatum activation as measured using functional magnetic resonance imaging (n=1,195).Results: In SPAN, SLEs prospectively predicted future depressive symptoms, especially among those reporting elevated N, even after accounting for prior depressive symptoms and previous SLE exposure (NxSLE interaction: p=0.016, ΔR2=0.003). In Study 2, we replicated this effect (NxSLE interaction: p=0.019, ΔR2=0.003). Further, neuroticism moderated the association between SLEs and reward-related left VS activity such that individuals with high neuroticism who were also exposed to more SLEs had blunted reward-related left VS activation (NxSLE: p=0.017, ΔR2=0.0048) which was associated with a lifetime depression diagnosis (r=-0.07, p=0.02), but not current depressive symptoms (r=-0.003, p=0.93).Conclusions: These data suggest that neuroticism may promote vulnerability to stress-related depression, and that sensitivity to stress-related VS dysfunction may be a potential neural mechanism underlying vulnerability to stress-related clinically significant depression.


2014 ◽  
Author(s):  
Pin-Hao Andy Chen ◽  
Paul J. Whalen ◽  
Jonathan B. Freeman ◽  
James M. Taylor ◽  
Todd F. Heatherton
Keyword(s):  

2016 ◽  
Author(s):  
Paula Nelas ◽  
Diana Gandara ◽  
Cláudia Chaves ◽  
Emília Coutinho ◽  
Carla Cruz ◽  
...  

Author(s):  
Lidia Bellés ◽  
Andrea Dimiziani ◽  
Stergios Tsartsalis ◽  
Philippe Millet ◽  
François R Herrmann ◽  
...  

Abstract Background Impulsivity and novelty preference are both associated with an increased propensity to develop addiction-like behaviors, but their relationship and respective underlying dopamine (DA) underpinnings are not fully elucidated. Methods We evaluated a large cohort (n = 49) of Roman high- and low-avoidance rats using single photon emission computed tomography to concurrently measure in vivo striatal D2/3 receptor (D2/3R) availability and amphetamine (AMPH)-induced DA release in relation to impulsivity and novelty preference using a within-subject design. To further examine the DA-dependent processes related to these traits, midbrain D2/3-autoreceptor levels were measured using ex vivo autoradiography in the same animals. Results We replicated a robust inverse relationship between impulsivity, as measured with the 5-choice serial reaction time task, and D2/3R availability in ventral striatum and extended this relationship to D2/3R levels measured in dorsal striatum. Novelty preference was positively related to impulsivity and showed inverse associations with D2/3R availability in dorsal striatum and ventral striatum. A high magnitude of AMPH-induced DA release in striatum predicted both impulsivity and novelty preference, perhaps owing to the diminished midbrain D2/3-autoreceptor availability measured in high-impulsive/novelty-preferring Roman high-avoidance animals that may amplify AMPH effect on DA transmission. Mediation analyses revealed that while D2/3R availability and AMPH-induced DA release in striatum are both significant predictors of impulsivity, the effect of striatal D2/3R availability on novelty preference is fully mediated by evoked striatal DA release. Conclusions Impulsivity and novelty preference are related but mediated by overlapping, yet dissociable, DA-dependent mechanisms in striatum that may interact to promote the emergence of an addiction-prone phenotype.


Author(s):  
Valery N. Mukhin ◽  
Ivan R. Borovets ◽  
Vadim V. Sizov ◽  
Konstantin I. Pavlov ◽  
Victor M. Klimenko

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