Theses and Dissertations
This collection includes both ASU Theses and Dissertations, submitted by graduate students, and the Barrett, Honors College theses submitted by undergraduate students.
Displaying 1 - 2 of 2
Filtering by
- All Subjects: Dopamine
Description
Fibromyalgia (FM) is a chronic musculoskeletal disorder characterized by widespread pain, fatigue, and a variety of other comorbid physiological and psychological characteristics, including a deficit of positive affect. Recently, the focus of research on the pathophysiology of FM has considered the role of a number of genomic variants. In the current manuscript, case-control analyses did not support the hypothesis that FM patients would differ from other chronic pain groups in catechol-O-methyltransferase (COMT) and mu-opioid receptor (OPRM1) genotype. However, evidence is provided in support of the hypothesis that functional single nucleotide polymorphisms on the COMT and OPRM1 genes would be associated with risk and resilience, respectively, in a dual processing model of pain-related positive affective regulation in FM. Forty-six female patients with a physician-confirmed diagnosis of FM completed an electronic diary that included once-daily assessments of positive affect and soft tissue pain. Multilevel modeling yielded a significant gene X environment interaction, such that individuals with met/met genotype on COMT experienced a greater decline in positive affect as daily pain increased than did either val/met or val/val individuals. A gene X environment interaction for OPRM1 also emerged, indicating that individuals with at least one asp allele were more resilient to elevations in daily pain than those homozygous for the asn allele. In sum, the findings offer researchers ample reason to further investigate the contribution of the catecholamine and opioid systems, and their associated genomic variants, to the still poorly understood experience of FM.
ContributorsFinan, Patrick Hamilton (Author) / Zautra, Alex (Thesis advisor) / Davis, Mary (Committee member) / Lemery-Chalfant, Kathryn (Committee member) / Presson, Clark (Committee member) / Arizona State University (Publisher)
Created2011
Description
Capacity limits of the human nervous system require important or rewarding information to be prioritized and encoded over less important or rewarding information. The present dissertation aims to identify structural and functional neural correlates of reward-motivated memory encoding. Chapter 1 reviews studies of reward-motivated memory encoding and their neural correlates, as well as the structure and function of dopaminergic midbrain circuits. Chapter 2 presents a study that utilizes electroencephalography (EEG) to determine which of two hypothesized processes underly the influence of reward value on episodic memory. One hypothesis is that value engages prefrontal executive control processes, so that valuable stimuli engage an elaborative rehearsal strategy that benefits memory. A second hypothesis is that value acts through the reward-related midbrain dopamine system to modulate synaptic plasticity in hippocampal and cortical efferents, thereby benefiting memory encoding. The results revealed that EEG signals thought to index dopamine-driven attention allocation were modulated by reward value and were positively correlated with individual differences in behavioral measures of memory prioritization. Chapter 3 employs diffusion-weighted magnetic resonance imaging (MRI) to dissociate heterogenous functional circuits of the midbrain reward system. The results comport with primate histology and show that midbrain circuits are differentially predictive of impulsivity and of attention-deficit hyperactivity disorder (ADHD). Chapter 4 presents a study that also employs diffusion-weighted MRI. The findings replicate Chapter 3 in dissociating heterogenous functional circuits of the midbrain reward system. Additionally, the structural integrity of midbrain-hippocampus circuits was quantified. Structural integrity of these circuits was positively correlated to behavioral measures of memory prioritization. These findings suggest that structural and functional measures of the dopaminergic reward system may underlie reward-motivated memory encoding in humans.
ContributorsElliott, Blake Louis (Author) / Brewer, Gene A (Thesis advisor) / McClure, Samuel M (Committee member) / Sanabria, Federico (Committee member) / Bae, Gi-Yeul (Committee member) / Arizona State University (Publisher)
Created2021