Brian J. Parks
Researcher
University of Arkansas for Medical Sciences
faculty
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Biography and Research Information
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Brian J. Parks conducts research focused on the pharmacological effects of substances, particularly in preclinical models. His work has investigated the pharmacodynamics of deuterated buprenorphine, examining its metabolism and its interaction with norbuprenorphine in the context of neonatal opioid withdrawal syndrome. Parks has also studied the impact of deuterated buprenorphine on mitigating fentanyl effects in pregnant rats. His research extends to the effects of early life adversity on substance use, including ethanol self-administration and adrenergic receptor expression in adolescent rats. Additionally, Parks has analyzed public discourse surrounding substances like kratom, examining responses to FDA inquiries and the motivations for self-medication. He has also contributed to the development and evaluation of surveys related to healthcare education, specifically for nurse practitioners.
Metrics
- h-index: 3
- Publications: 12
- Citations: 29
Selected Publications
- Development and Psychometric Evaluation of a Theory-Based Preceptorship Survey for Nurse Practitioners (2025) DOI
- Limited bedding and nesting increases ethanol drinking in female rats (2024) DOI
- Interaction between buprenorphine and norbuprenorphine in neonatal opioid withdrawal syndrome (2023) DOI
- Deuterated buprenorphine retains pharmacodynamic properties of buprenorphine and resists metabolism to the active metabolite norbuprenorphine in rats (2023) DOI
- Effects of a two-hit model of early life adversity on oral ethanol self-administration and adrenergic receptor expression in adolescent rats (2023) DOI
- 481 Interactions between buprenorphine and norbuprenorphine in neonatal opioid withdrawal syndrome (2023) DOI
- Interaction between buprenorphine and norbuprenorphine in neonatal opioid withdrawal syndrome. (2022) DOI
- Deuterated buprenorphine retains pharmacodynamic properties of buprenorphine and resists metabolism to the active metabolite norbuprenorphine in rats (2022) DOI
- Qualitative content analysis of public responses to an FDA inquiry on the impact of scheduling changes to kratom (2022) DOI
- Effects of prenatal opioid exposure and early life adversity on opioidâinduced antinociception (2022) DOI
- 384 Motives for kratom self-medication: contents of public comments solicited by the FDA (2022) DOI
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