Chronobiology international
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Accumulating evidence suggests epilepsy and seizures may influence circadian rhythms and that circadian rhythms may influence epilepsy. It is also conceivable that seizure timing influences the timing of daily activities, sleeping, and wakefulness (i.e., chronotype). Only one group has studied the distribution of chronotypes of epileptics, showing significant differences between the diurnal activity patterns in two groups of patients with different epilepsy syndromes. ⋯ We show that the distribution of chronotypes and subjective sleep parameters of epileptics, in general, is different from that of healthy controls. Nevertheless, no differences are observed between patients with specified epilepsy syndromes, although they exhibit seizures with different diurnal patterns. Our results suggest that epilepsy, itself, rather than seizure timing, has a significant influence on chronotype behavior and subjective sleep parameters.
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Pain exhibits temporal variations in intensity due to multiple factors, including endogenous neuroendocrine and various external influences that vary over the 24 h. Also, medications can vary in potency and/or toxicity according to the time when they are administered. However, there is no consensus among studies regarding the 24-h pattern of analgesia during labor. ⋯ However, the duration of intrathecal analgesia showed two peaks, i.e., at approximately 00:00 and approximately 12:00 h. These results demonstrate that labor analgesia achieved by fentanyl combined with bupivacaine shows a diurnal pattern in pain relief and duration of spinal analgesia. However, part of these temporal patterns was explained by the association with duration of labor.
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The present study determined a circadian rhythm in force control during a visually guided tracking task under single task conditions (i.e., tracking task presented alone) and dual task conditions (i.e., tracking task together with a memory task). Nine healthy young male subjects participated in a Constant Routine protocol involving a week of regular bedtimes, a baseline night of 8 h sleep, and subsequent wakefulness of 40 h. Subjects performed an eye-hand coordination task that required tracking an unpredictable target (presented on a computer screen) by using grip force to adjust a visual feedback to the changing target. ⋯ Tracking precision descriptively revealed inter-individual differences: half of the subjects maintained fairly stable performance during the 40 h of wakefulness, whereas the other half showed a clear circadian rhythmicity in tracking precision. Thus, tracking precision seems to be a sensitive parameter for conditions of divided attention and inter-individual variability during the circadian minimum, whereas tracking delay revealed neither a dichotomy of task conditions nor inter-individual differences in performance-amplitude over sessions. Nonetheless, both tracking precision and delay showed a comparable circadian rhythmicity.
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Melatonin, which shows a robust nycthemeral rhythm, plays the role of an endogenous synchronizer, able to stabilize and reinforce circadian rhythms and maintain their mutual phase relationships. Additionally, melatonin is a potent antioxidant and displays immunological properties. Because free radical generation, immune dysfunction, and sleep and metabolic disorders are involved in the short- and long-term pathophysiology of the burn syndrome, we undertook the study of daily urine melatonin, 6-sulfatoxymelatonin (aMT6s, the main hepatic melatonin metabolite), and cortisol variations plus temperature profiles in burn patients using a non-invasive protocol. ⋯ The core temperature profiles were abnormal in all three sessions, mainly during the night, although there was a tendency toward normalization with time. The individual mesors were consistently increased compared with controls. Globally, the abnormalities we report could participate in the pathophysiology of short- and long-term alterations observed in burn syndrome, especially disturbances of sleep, metabolism, and immune function.
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Long-term, night shiftwork has been identified as a potential carcinogenic risk factor. It is hypothesized that increased light at night exposure during shiftwork reduces melatonin production, which is associated with increased cancer risk. Sleep duration has been hypothesized to influence both melatonin levels and cancer risk, and it has been suggested that sleep duration could be used as a proxy for melatonin production. ⋯ Analysis of salivary melatonin levels indicated that the circadian rhythms of night workers were not altered, meaning peak melatonin production occurred at night. This study indicates that two nights of rotating shift work may not change the timing of melatonin production to the day among those working at night. Additionally, in this study, sleep duration was not correlated with urinary melatonin levels, suggesting it may not be a good proxy for melatonin production.