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Biography and Research Information
OverviewAI-generated summary
Brenda M. Gannon's research focuses on the abuse-related effects of drugs and drug mixtures, particularly synthetic cathinones and novel arylcyclohexylamines. Her work investigates the interactions of these substances with monoamine transporters, such as the norepinephrine transporter, and their impact on behavior in rodent models. Gannon has published on the development of cannabinoids as therapeutic agents and the role of the endocannabinoid system in alcohol dependence. Her studies also examine phencyclidine-like abuse liability and psychosis-like neurocognitive effects of novel drugs. Gannon is affiliated with the University of Arkansas for Medical Sciences and has a notable number of shared publications with collaborators including William E. Fantegrossi and Lauren R. Fitzgerald. Her scholarship includes 50 publications and a h-index of 16, with 906 total citations.
Metrics
- h-index: 16
- Publications: 51
- Citations: 911
Selected Publications
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Abuse potential assessment of novel central nervous system active and psychedelic substances for controlled substances act scheduling recommendations (2025)
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Effects of orally self-administered furanyl fentanyl and acryl fentanyl in mice: antinociception, dependence and withdrawal, and defense of consumption (2025)
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A “Furious” Effort to Develop Novel 3,4-Methylenedioxymethamphetamine-Like Therapeutics (2024)
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Respiratory Depressant Effects of Fentanyl in Combination With Synthetic Cannabinoid Receptor Agonists: A Potential Mechanism for “Narcan-Resistant” Overdose (2024)
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The Development of Cannabinoids as Therapeutic Agents in the United States (2024)
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Erratum to “Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety” [Drug Alcohol Depend. 250 (2023) 110917] (2024)
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Phencyclidine-Like Abuse Liability and Psychosis-Like Neurocognitive Effects of Novel Arylcyclohexylamine Drugs of Abuse in Rodents (2024)
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Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones (2023)
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Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety (2023)
Collaboration Network
Top Collaborators
- Effects of Laboratory Housing Conditions on Core Temperature and Locomotor Activity in Mice
- Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones
- Phencyclidine-Like Abuse Liability and Psychosis-Like Neurocognitive Effects of Novel Arylcyclohexylamine Drugs of Abuse in Rodents
- Abuse potential assessment of novel central nervous system active and psychedelic substances for controlled substances act scheduling recommendations
- Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety
Showing 5 of 9 shared publications
- Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones
- Phencyclidine-Like Abuse Liability and Psychosis-Like Neurocognitive Effects of Novel Arylcyclohexylamine Drugs of Abuse in Rodents
- Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety
- Erratum to “Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety” [Drug Alcohol Depend. 250 (2023) 110917]
- MDPV “high-responder” rats also self-administer more oxycodone than their “low-responder” counterparts under a fixed ratio schedule of reinforcement
- Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety
- Erratum to “Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety” [Drug Alcohol Depend. 250 (2023) 110917]
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
- MDPV “high-responder” rats also self-administer more oxycodone than their “low-responder” counterparts under a fixed ratio schedule of reinforcement
- The Endocannabinoid System and Alcohol Dependence: Will CannabinoidReceptor 2 Agonism be More Fruitful than Cannabinoid Receptor 1 Antagonism?
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
- Structure-activity relationships for locomotor stimulant effects and monoamine transporter interactions of substituted amphetamines and cathinones
- Application of dose‐addition analyses to characterize the abuse‐related effects of drug mixtures
- Abuse potential assessment of novel central nervous system active and psychedelic substances for controlled substances act scheduling recommendations
- Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety
- Erratum to “Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety” [Drug Alcohol Depend. 250 (2023) 110917]
- Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety
- Erratum to “Effects of ambient temperature on locomotor activity and place conditioning elicited by abused psychostimulants in mice: Role of 3,4-methylenedioxy moiety” [Drug Alcohol Depend. 250 (2023) 110917]
- Phencyclidine-Like Abuse Liability and Psychosis-Like Neurocognitive Effects of Novel Arylcyclohexylamine Drugs of Abuse in Rodents
- Effects of orally self-administered furanyl fentanyl and acryl fentanyl in mice: antinociception, dependence and withdrawal, and defense of consumption
- The Development of Cannabinoids as Therapeutic Agents in the United States
- Abuse potential assessment of novel central nervous system active and psychedelic substances for controlled substances act scheduling recommendations
- The Endocannabinoid System and Alcohol Dependence: Will CannabinoidReceptor 2 Agonism be More Fruitful than Cannabinoid Receptor 1 Antagonism?
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
- α-PPP and its derivatives are selective partial releasers at the human norepinephrine transporter
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