Browsing by Author "Feng, Shengchuang"

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    Association between Reward Sensitivity and Smoking Status in Major Depressive Disorder
    Feng, Shengchuang (Virginia Tech, 2017-05-10)
    Chronic nicotine use has been linked to increased sensitivity to nondrug rewards as well as improvement in mood among individuals with depression, and these effects have been hypothesized to be mediated through alternations in striatal dopamine activity. Similarly, chronic nicotine use is hypothesized to influence the mechanisms by which healthy and depressed individuals learn about rewards in their environment. However, the specific behavioral and neural mechanisms by which nicotine influences the learning process is poorly understood. Here, we use a probabilistic learning task, functional magnetic resonance imaging and neurocomputational analyses, to show that chronic smoking is associated with higher reward sensitivity, along with lower learning rate and striatal prediction error signal. Further, we show that these effects do not differ between individuals with and without major depressive disorder (MDD). In addition, a negative correlation between reward sensitivity and striatal prediction error signal was found among smokers, consistent with the suggestion that enhanced tonic dopamine associated with increased reward sensitivity leads to an attenuation of phasic dopamine activity necessary for updating of reward value during learning.
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    Self- and other-regarding reinforcement learning: Disruptions in mental disorders and oxytocin's modulating role in healthy people
    Feng, Shengchuang (Virginia Tech, 2020-06-17)
    It has been suggested that reward processing and related neural substrates are disrupted in some common mental disorders such as depression, addiction, and anxiety. An increasing number of psychiatric studies have been applying reinforcement learning (RL) models to examine these disruptions in self-regarding learning (learning about rewards delivered to the learners themselves). A review of RL alterations associated with mental disorders in extant studies will be beneficial for uncovering the mechanisms of these health problems. Although impaired social reward processing is common in some mental disorders [e.g., post-traumatic stress disorder (PTSD), social anxiety and autism], RL has not been widely used to detect the potentially disrupted social reward learning, especially for other-regarding learning (learning about rewards delivered to others). Meanwhile, it has not been clear whether some drugs, e.g., oxytocin (OT), can alter other-regarding learning, so they may serve as a therapeutic intervention when related deficits occur. In the present set of studies, we summarized common and distinct features in terms of self-regarding RL disturbances among depression, addiction and anxiety disorders based on previous findings (Paper I), tested whether behavioral and neural self- and other-regarding RL were impaired in PTSD with and without comorbid depression (Paper II), and investigated OT's behavioral and neural effects on self- and other-regarding RL in healthy males (Paper III). The results of our literature review showed that the commonalities in all three mental disorders were inflexibility and inconsistent choices, and the differences included decreased learning rates in depression, a higher weight to rewards versus punishments in addiction, and hypersensitivity to punishments in anxiety. The results of the PTSD study demonstrated impaired behavioral other-regarding learning in PTSD patients with and without depression, supposedly due to their hypervigilance to unexpected outcomes for others, as evidenced by the heightened responses in their inferior parietal lobule. The OT study detected OT's effects of attenuating behavioral other-regarding learning, as well as the neural coding of unexpected outcomes for others in the anterior cingulate cortex. These findings provide new evidence of self- and other-regarding RL alterations in mental disorders, reveal potential targets for their treatments, and bring caution for using OT as a therapeutic intervention.
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    Validation of a novel method of ultraviolet-induced cutaneous inflammation and its associations with anhedonia
    Sullivan-Toole, Holly; Feng, Shengchuang; Carlton, Corinne N.; Ghane, Merage; Olino, Thomas M.; Allen, Irving C.; Richey, John A. (Nature Portfolio, 2022-11)
    Affective immunology of the skin is a growing area; however, established protocols for measuring individual differences in cutaneous inflammation are lacking. To address this, we present a preliminary validation of Precision Implementation of Minimal Erythema Dose (PI-MED) testing as a method for measuring cutaneous inflammation. PI-MED is a recently adapted protocol, optimized for reproducibility and individual differences research, that uses ultraviolet (UV) light to evoke cutaneous erythema, or inflammatory skin reddening. PI-MED's novel UV dosage schedule produces standardized erythema responses across different skin pigmentation types and shows strong internal consistency within person and good test-retest reliability across 8-10 weeks. In line with predictions, increased PI-MED erythema was associated with heightened anhedonia, across several measures, beyond influences of non-affective covariates. While future work should further refine the dosage schedule for the lightest and darkest skin types, overall, evidence supports PI-MED as a protocol for inducing and measuring individual differences in cutaneous inflammation. Further, PI-MED-induced erythema can expand psychoneuroimmunology research by offering a complementary assessment for general inflammatory tone. This work adds to a growing body of evidence demonstrating a distinct relationship between inflammation and anhedonia.