Animal model of methylphenidate's long-term memory-enhancing effects

Autor: Stephan G. Anagnostaras, Kleou Rasaei, Kristin K. Howell, Emilie T. Reas, Stephanie A. Carmack
Rok vydání: 2014
Předmět:
Male
Conditioning
Classical

Pharmacology
Inbred C57BL
Atomoxetine Hydrochloride
Medical and Health Sciences
Developmental psychology
Mice
Cocaine
Psychology
Fear conditioning
Nootropic Agents
Propylamines
Adrenergic Uptake Inhibitors
Long-term memory
Methylphenidate
Fear
Biological Sciences
Reinforcement
Mental Health
Neuropsychology and Physiological Psychology
Serotonin Uptake Inhibitors
Attention Deficit Disorder (ADD)
Female
Drug
Reinforcement
Psychology

Selective Serotonin Reuptake Inhibitors
Locomotion
medicine.drug
Atomoxetine hydrochloride
Memory
Long-Term

Cognitive Neuroscience
Citalopram
Long-Term
Basic Behavioral and Social Science
Dose-Response Relationship
Cellular and Molecular Neuroscience
Memory
Behavioral and Social Science
mental disorders
medicine
Animals
Attention deficit hyperactivity disorder
Maze Learning
Amphetamine
Bupropion
Neurology & Neurosurgery
Dose-Response Relationship
Drug

Research
Psychology and Cognitive Sciences
Atomoxetine
Neurosciences
medicine.disease
Conditioned place preference
Classical
Brain Disorders
Mice
Inbred C57BL

Reinforcement (Psychology)
Space Perception
Central Nervous System Stimulants
Conditioning
Zdroj: Learning & memory (Cold Spring Harbor, N.Y.), vol 21, iss 2
Carmack, SA; Howell, KK; Rasaei, K; Reas, ET; & Anagnostaras, SG. (2014). Animal model of methylphenidate's long-term memory-enhancing effects. Learning and Memory, 21(2), 82-89. doi: 10.1101/lm.033613.113. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/0wg3c8z0
ISSN: 1549-5485
DOI: 10.1101/lm.033613.113
Popis: Methylphenidate (MPH), introduced more than 60 years ago, accounts for two-thirds of current prescriptions for attention deficit hyperactivity disorder (ADHD). Although many studies have modeled MPH's effect on executive function, almost none have directly modeled its effect on long-term memory (LTM), even though improvement in LTM is a critical target of therapeutic intervention in ADHD. We examined the effects of a wide range of doses of MPH (0.01-10 mg/kg, i.p.) on Pavlovian fear learning, a leading model of memory. MPH's effects were then compared to those of atomoxetine (0.1-10 mg/kg, i.p.), bupropion (0.5-20 mg/kg, i.p.), and citalopram (0.01-10 mg/kg, i.p.). At low, clinically relevant doses, MPH enhanced fear memory; at high doses it impaired memory. MPH's memory-enhancing effects were not confounded by its effects on locomotion or anxiety. Further, MPH-induced memory enhancement seemed to require both dopamine and norepinephrine transporter inhibition. Finally, the addictive potential of MPH (1 mg/kg and 10 mg/kg) was compared to those of two other psychostimulants, amphetamine (0.005 mg/kg and 1.5 mg/kg) and cocaine (0.15 mg/kg and 15 mg/kg), using a conditioned place preference and behavioral sensitization paradigm. We found that memory-enhancing effects of psychostimulants observed at low doses are readily dissociable from their reinforcing and locomotor activating effects at high doses. Together, our data suggest that fear conditioning will be an especially fruitful platform for modeling the effects of psychostimulants on LTM in drug development. © 2014 Carmack et al.
Databáze: OpenAIRE