TY - JOUR
T1 - Serotonergic integration of circadian clock and ultradian sleep-wake cycles
AU - Miyamoto, Hiroyuki
AU - Nakamaru-Ogiso, Eiko
AU - Hamada, Kozo
AU - Hensch, Takao K.
PY - 2012/10/17
Y1 - 2012/10/17
N2 - In mammals, the suprachiasmatic nucleus (SCN) of the hypothalamus generates a 24 h rhythm of sleep and arousal. While neuronal spiking activity in the SCN provides a functional circadian oscillator that propagates throughout the brain, the ultradian sleep-wake state is regulated by the basal forebrain/preoptic area (BF/POA). How this SCN circadian oscillation is integrated into the shorter sleep-wake cycles remains unclear. We examined the temporal patterns of neuronal activity in these key brain regions in freely behaving rats. Neuronal activity in various brain regions presented diurnal rhythmicity and/or sleep-wake state dependence. We identified a diurnal rhythm in the BF/POA that was selectively degraded when diurnal arousal patterns were disrupted by acute brain serotonin depletion despite robust circadian spiking activity in the SCN. Local blockade of serotonergic transmission inthe BF/POA was sufficient to disrupt the diurnal sleep-wake rhythm of mice. These results suggest that the serotonergic system enables the BF/POA to couple the SCN circadian signal to ultradian sleep-wake cycles, thereby providing apotential link between circadian rhythms and psychiatric disorders.
AB - In mammals, the suprachiasmatic nucleus (SCN) of the hypothalamus generates a 24 h rhythm of sleep and arousal. While neuronal spiking activity in the SCN provides a functional circadian oscillator that propagates throughout the brain, the ultradian sleep-wake state is regulated by the basal forebrain/preoptic area (BF/POA). How this SCN circadian oscillation is integrated into the shorter sleep-wake cycles remains unclear. We examined the temporal patterns of neuronal activity in these key brain regions in freely behaving rats. Neuronal activity in various brain regions presented diurnal rhythmicity and/or sleep-wake state dependence. We identified a diurnal rhythm in the BF/POA that was selectively degraded when diurnal arousal patterns were disrupted by acute brain serotonin depletion despite robust circadian spiking activity in the SCN. Local blockade of serotonergic transmission inthe BF/POA was sufficient to disrupt the diurnal sleep-wake rhythm of mice. These results suggest that the serotonergic system enables the BF/POA to couple the SCN circadian signal to ultradian sleep-wake cycles, thereby providing apotential link between circadian rhythms and psychiatric disorders.
UR - http://www.scopus.com/inward/record.url?scp=84867585936&partnerID=8YFLogxK
U2 - 10.1523/JNEUROSCI.0793-12.2012
DO - 10.1523/JNEUROSCI.0793-12.2012
M3 - Article
C2 - 23077063
AN - SCOPUS:84867585936
SN - 0270-6474
VL - 32
SP - 14794
EP - 14803
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 42
ER -