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1.
Learn Mem ; 28(6): 195-203, 2021 06.
Article in English | MEDLINE | ID: mdl-34011516

ABSTRACT

Sleep following learning facilitates the consolidation of memories. This effect has often been attributed to sleep-specific factors, such as the presence of sleep spindles or slow waves in the electroencephalogram (EEG). However, recent studies suggest that simply resting quietly while awake could confer a similar memory benefit. In the current study, we examined the effects of sleep, quiet rest, and active wakefulness on the consolidation of declarative and procedural memory. We hypothesized that sleep and eyes-closed quiet rest would both benefit memory compared with a period of active wakefulness. After completing a declarative and a procedural memory task, participants began a 30-min retention period with PSG (polysomnographic) monitoring, in which they either slept (n = 24), quietly rested with their eyes closed (n = 22), or completed a distractor task (n = 29). Following the retention period, participants were again tested on their memory for the two learning tasks. As hypothesized, sleep and quiet rest both led to better performance on the declarative and procedural memory tasks than did the distractor task. Moreover, the performance advantages conferred by rest were indistinguishable from those of sleep. These data suggest that neurobiology specific to sleep might not be necessary to induce the consolidation of memory, at least across very short retention intervals. Instead, offline memory consolidation may function opportunistically, occurring during either sleep or stimulus-free rest, provided a favorable neurobiological milieu and sufficient reduction of new encoding.


Subject(s)
Memory Consolidation , Humans , Learning , Rest , Sleep , Wakefulness
2.
Neuropharmacology ; 183: 108325, 2021 02 01.
Article in English | MEDLINE | ID: mdl-32956676

ABSTRACT

Depressed individuals suffer from effort-related motivational symptoms such as anergia and fatigue, which are resistant to treatment with many common antidepressants. While drugs that block dopamine transport (DAT) reportedly have positive motivational effects, DAT inhibitors such as cocaine and amphetamines produce undesirable side effects. Thus, there is a need to develop and characterize novel atypical DAT inhibitors with unique and selective binding profiles. Rodent effort-based choice tasks provide useful models of motivational dysfunctions. With these tasks, animals choose between a high-effort instrumental action leading to highly valued reinforcement vs. a low effort/low reward option. The present studies focused on the initial characterization of a novel atypical DAT inhibitor, CT-005404, which binds to DAT with high selectivity relative to serotonin and norepinephrine transport, and produces long-term elevations of extracellular DA. CT-005404 was assessed for its ability to attenuate the effort-related motivational effects of the DA depleting agent tetrabenazine and the pro-inflammatory cytokine interleukin-1ß (IL-1ß) using a fixed ratio 5/chow feeding choice test. Tetrabenazine (1.0 mg/kg i.p.) shifted choice behavior, decreasing lever pressing and increasing chow intake. IL-1ß (4.0 µg/kg i.p.) also decreased lever pressing. CT-005404 was co-administered (7.5-30.0 mg/kg p.o.) with either tetrabenazine or IL-1ß, and the 15.0 and 30.0 mg/kg doses significantly reversed the effects of tetrabenazine and IL-1ß. CT-005404 administered alone produced a dose-related increase in lever pressing in rats tested on a progressive ratio/chow feeding choice task. Atypical DAT inhibitors such as CT-005404 offer potential as a new avenue for drug treatment of motivational dysfunctions in humans.


Subject(s)
Choice Behavior/drug effects , Conditioning, Operant/drug effects , Depression/drug therapy , Dopamine Plasma Membrane Transport Proteins/antagonists & inhibitors , Tetrabenazine/pharmacology , Vesicular Monoamine Transport Proteins/antagonists & inhibitors , Animals , Dopamine Plasma Membrane Transport Proteins/metabolism , Feeding Behavior/drug effects , Interleukin-1beta/pharmacology , Male , Nucleus Accumbens/drug effects , Rats , Rats, Sprague-Dawley , Reward
3.
Mem Cognit ; 48(8): 1346-1358, 2020 11.
Article in English | MEDLINE | ID: mdl-32562248

ABSTRACT

Prior research has demonstrated that Americans massively overestimate how much their home state has contributed to US history. Why does such collective overclaiming occur? We argue that although self-serving biases undoubtedly influence overclaiming, non-motivated factors, such as a failure to consider the contributions of other states, also play a large role in overclaiming effects. In the current studies, subjects read descriptions of territories within a fictitious country and evaluated how much a territory within that country contributed to its history. Experiment 1 showed that overclaiming of responsibility increased as more territories were added to the country. Experiments 2 and 3 showed that requiring subjects to explicitly consider all territories reduced estimations of responsibility. Experiment 4 showed that people provided higher ratings of responsibility when more details were provided about the territory. Finally, Experiment 5 showed that retrieval fluency did not affect overclaiming. We conclude that support theory - based on the availability of content - provides a strong explanation for why the collective overclaiming of responsibility occurs, with both theoretical and practical implications.


Subject(s)
Moral Status , Humans , United States
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