Adolescence is a period of the lifespan when challenges to behavioral regulation can have critical short and long-term repercussions. During adolescence, burgeoning independence and exposure to situations that entail tangible risk (access to alcohol, drugs, or cigarettes) present a particular psychological challenge, whereby momentary motivation toward potential rewards comes into conflict with long-term goals that require inhibitory control processes. Though risky decision-making remains a key public health issue in adolescence, there is not a clear consensus on how to best design public health interventions to support decision making in adolescence. If we understood the mechanisms of inhibitory control, specifically in the face of rewarding stimuli we could create more effective interventions around risk in adolescence. Age related variability in self-regulatory behavior and resulting risky behavior during adolescence has been historically attributed to age-related deficits in inhibitory control and still-maturing lateral prefrontal systems, such as the right infrior frontal gyrus. However, recent neuroimaging studies have challenged this view (for a review, see Somerville, Jones, & Casey, 2010). For example, most motor inhibitory control tasks improve during adolescence, instead of declining. However, one study revealed that adolescents (relative to children and adults) were selectively less skilled at engaging in impulse control to positive social cues (happy faces) and showed different associated patterns of activity in the ventral striatum (VS). While this evidence suggests that increased risk behavior during adolescence may stem from adolescent-specific challenges in employing inhibitory control over rewarding cues, this task relies heavily on social stimuli (smiling faces), which come with their own variable reactions, known to be influenced by early childhood experiences and onset of adolescence. Here we address these gaps in the literature by introducing a novel test of inhibition of reward Learned Reward Inhibition Task (LRIT) and propose to investigate the neural correlates of the developmental progression of inhibition of reward across late childhood, early adolescence, late adolescence and adulthood using structural and functional MRI. Our preliminary data suggest differences between children and adolescents in control over previously rewarded, socially irrelevant stimuli. In children, inhibition is facilitated for these stimui, while it is selectively impaired in adolescents. That is, in the LRIT task, children are moe able to withhold a response from a previously rewarded cue. In contrast, adolescents are less able to withhold a response from a previously rewarded cue. This task, relative to other assessments of inhibitory control, appears to isolate a deficit in adolescent cognition, relative t children that more closely aligns with the dramatic uptick in risk taking and self reported impulsivity in adolescence.

Public Health Relevance

To date, studies of the neural correlates of inhibitory control during adolescence have clear limitations and are poorly understood, representing a gap in knowledge with implications for a major public health concern. Here we address this gap in the literature by introducing a novel test of inhibitory control over reward: Learned Reward Inhibition Task (LRIT) and propose to investigate the neural correlates of the developmental progression of inhibitory control over adolescence and associations with substance use/abuse. This task, relative to other assessments of inhibitory control, isolates deficits in adolescent cognition, relative to children that most closely aligns with the dramatic uptick in risk taking and self reported impulsivity in adolescence.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Small Research Grants (R03)
Project #
1R03DA037405-01A1
Application #
8823083
Study Section
Special Emphasis Panel (ZDA1-MXL-F (03))
Program Officer
Grant, Steven J
Project Start
2015-02-01
Project End
2016-01-31
Budget Start
2015-02-01
Budget End
2016-01-31
Support Year
1
Fiscal Year
2015
Total Cost
$215,297
Indirect Cost
$65,297
Name
Children's Hospital Boston
Department
Type
DUNS #
076593722
City
Boston
State
MA
Country
United States
Zip Code
02115
Sheridan, Margaret A; McLaughlin, Katie A; Winter, Warren et al. (2018) Early deprivation disruption of associative learning is a developmental pathway to depression and social problems. Nat Commun 9:2216
Busso, Daniel S; McLaughlin, Katie A; Sheridan, Margaret A (2017) Dimensions of Adversity, Physiological Reactivity, and Externalizing Psychopathology in Adolescence: Deprivation and Threat. Psychosom Med 79:162-171
Busso, Daniel S; McLaughlin, Katie A; Brueck, Stephanie et al. (2017) Child Abuse, Neural Structure, and Adolescent Psychopathology: A Longitudinal Study. J Am Acad Child Adolesc Psychiatry 56:321-328.e1
LeWinn, Kaja Z; Sheridan, Margaret A; Keyes, Katherine M et al. (2017) Sample composition alters associations between age and brain structure. Nat Commun 8:874
Gold, Andrea L; Sheridan, Margaret A; Peverill, Matthew et al. (2016) Childhood abuse and reduced cortical thickness in brain regions involved in emotional processing. J Child Psychol Psychiatry 57:1154-64
McLaughlin, Katie A; Sheridan, Margaret A; Winter, Warren et al. (2014) Widespread reductions in cortical thickness following severe early-life deprivation: a neurodevelopmental pathway to attention-deficit/hyperactivity disorder. Biol Psychiatry 76:629-38
Sheridan, Margaret A; McLaughlin, Katie A (2014) Dimensions of early experience and neural development: deprivation and threat. Trends Cogn Sci 18:580-585
Law, Evelyn C; Sideridis, Georgios D; Prock, Lisa Albers et al. (2014) Attention-deficit/hyperactivity disorder in young children: predictors of diagnostic stability. Pediatrics 133:659-67
Winter, Warren; Sheridan, Margaret (2014) Previous reward decreases errors of commission on later 'No-Go' trials in children 4 to 12 years of age: evidence for a context monitoring account. Dev Sci 17:797-807
Kharitonova, Maria; Martin, Rebecca E; Gabrieli, John D E et al. (2013) Cortical gray-matter thinning is associated with age-related improvements on executive function tasks. Dev Cogn Neurosci 6:61-71