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Am J Physiol Regul Integr Comp Physiol (November 17, 2005). doi:10.1152/ajpregu.00304.2005
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Submitted on April 29, 2005
Accepted on November 5, 2005

Altered Sleep Regulation in Leptin Deficient Mice

Aaron D Laposky1*, Jonathan Shelton1, Joseph Bass2, Christine Dugovic1, Nicholas Perrino3, and Fred W Turek1

1 Neurobiology and Physiology, Northwestern University, Evanston, IL, USA; Center for Sleep and Circadian Biology, Northwestern University, Evanston, IL, USA
2 Neurobiology and Physiology, Northwestern University, Evanston, IL, USA; Center for Sleep and Circadian Biology, Northwestern University, Evanston, IL, USA; Endocrinology, Evanston Northwestern Hospital, Evanston, IL, USA
3 Neurobiology and Physiology, Northwestern University, Evanston, IL, USA

* To whom correspondence should be addressed. E-mail: a-laposky{at}northwestern.edu.

Recent epidemiological, clinical and experimental studies have demonstrated important links between sleep duration and architecture, circadian rhythms and metabolism, although the genetic pathways that may interconnect these processes are not well understood. Leptin is a circulating hormone and major adiposity signal involved in long-term energy homeostasis. In this study, we tested the hypothesis that leptin deficiency leads to impairments in sleep-wake regulation. Male ob/ob mice, a genetic model of leptin deficiency, had significantly disrupted sleep architecture with an elevated number of arousals from sleep (wt, 108.2±7.2 vs. ob/ob, 148.4±4.5, P<.001) and increased stage shifts (wt, 519.1±25.2 vs. ob/ob, 748.0±38.8, P<.001) compared to wild type (wt) mice. Ob/ob mice also had more frequent, but shorter lasting sleep bouts compared to wt mice, indicating impaired sleep consolidation. Interestingly, ob/ob mice showed changes in sleep time, with increased amounts of 24-hr NREM sleep (wt, 601.5±10.8 vs. ob/ob, 669.2±13.4 minutes, P<.001). Ob/ob mice had overall lower body temperature (wt, 35.1±0.2 vs. ob/ob, 33.4±0.2 °C, P<.001) and locomotor activity counts (wt, 25125±2137 vs. ob/ob, 5219±1759, P<.001). Ob/ob mice displayed an attenuated diurnal rhythm of sleep-wake stages, NREM delta power and locomotor activity. Following sleep deprivation, ob/ob mice had smaller amounts of NREM and REM recovery sleep, both in terms of the magnitude and the duration of the recovery response. In combination, these results indicate that leptin deficiency disrupts the regulation of sleep architecture and diurnal rhythmicity.




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