2014
DOI: 10.1016/j.bbr.2014.03.048
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The effect of constant darkness and circadian resynchronization on the recovery of alcohol hangover

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Cited by 6 publications
(4 citation statements)
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References 40 publications
(34 reference statements)
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“…Mice were acclimated to constant dark for 6 weeks, and livers were harvested at 9:00 am (CT1), and then every 4 h (CT5, CT9, CT13, CT17, and CT21). RNA-Seq data was presented as reads count of pooled samples hangover swiss mice [53]. Profiling genes circadian rhythm under L-DD is important for metabolic study.…”
Section: Discussionmentioning
confidence: 99%
“…Mice were acclimated to constant dark for 6 weeks, and livers were harvested at 9:00 am (CT1), and then every 4 h (CT5, CT9, CT13, CT17, and CT21). RNA-Seq data was presented as reads count of pooled samples hangover swiss mice [53]. Profiling genes circadian rhythm under L-DD is important for metabolic study.…”
Section: Discussionmentioning
confidence: 99%
“…Thus, at the same phase, circadian modulation results in decreased sensitivity to the sedative properties of alcohol and speeds the recovery process from those sedative effects. In mice, the circadian clock affects recovery from alcohol hangover symptoms, including motor coordination and anxiety, with constant darkness shortening recovery periods and circadian desynchronization inhibiting the recovery (Karadayian et al, 2014). We found that the absence of a functional circadian clock in per 01 mutants significantly increased the time necessary to recover from the sedative effects of alcohol.…”
Section: Discussionmentioning
confidence: 99%
“…hangover was developed, demonstrating long-lasting motor and affective impairments for at least 14-20 h post hangover onset [46][47][48]. Based on this model, the after-effects of acute ethanol exposure were associated with an imbalance in free radical and antioxidant production, together with decreases in oxygen consumption, inhibition of respiratory chain complex enzymatic activity, and decreases in mitochondrial membrane potential in the mouse brain cortex and cerebellum [46,[49][50][51].…”
Section: Pathology and Treatmentmentioning
confidence: 99%