The Mammalian Circadian Clock in the Suprachiasmatic Nucleus Exhibits Rapid Tolerance to Ethanol In Vivo and In Vitro

被引:10
|
作者
Lindsay, Jonathan H. [1 ]
Glass, J. David [2 ]
Amicarelli, Mario [2 ]
Prosser, Rebecca A. [1 ]
机构
[1] Univ Tennessee, Dept Biochem & Cellular & Mol Biol, Knoxville, TN 37996 USA
[2] Kent State Univ, Dept Biol Sci, Kent, OH 44242 USA
关键词
Rapid Tolerance; Ethanol; Circadian Rhythms; Suprachiasmatic Nucleus; Glutamate; GABAERGIC SYNAPTIC-TRANSMISSION; PHASE-SHIFTS; ALCOHOL-CONSUMPTION; GABA(A) RECEPTORS; FYN-KINASE; SENSITIVITY; SLEEP; LIGHT; DISRUPTION; EXPOSURE;
D O I
10.1111/acer.12303
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
BackgroundEthanol (EtOH) triggers cellular adaptations that induce tolerance in many brain areas, including the suprachiasmatic nucleus (SCN), the site of the master circadian clock. EtOH inhibits light-induced phase shifts in the SCN in vivo and glutamate-induced phase shifts in vitro. The in vitro phase shifts develop acute tolerance to EtOH, occurring within minutes of initial exposure, while the in vivo phase shifts exhibit no evidence of chronic tolerance. An intermediate form, rapid tolerance, is not well studied but may predict subsequent chronic tolerance. Here, we investigated rapid tolerance in the SCN clock. MethodsAdult C57BL/6mice were provided 15% EtOH or water for one 12-hour lights-off period. For in vitro experiments, SCN-containing brain slices were prepared in the morning and treated for 10minutes with glutamate +/- EtOH the following night. Single-cell neuronal firing rates were recorded extracellularly during the subsequent day to determine SCN clock phase. For in vivo experiments, mice receiving EtOH 24hours previously were exposed to a 30-minute light pulse immediately preceded by intraperitoneal saline or 2g/kg EtOH injection. Mice were then placed in constant darkness and their phase-shifting responses measured. ResultsIn vitro, the SCN clock from EtOH-exposed mice exhibited rapid tolerance, with a 10-fold increase in EtOH needed to inhibit glutamate-induced phase shifts. Co-application of brain-derived neurotrophic factor prevented EtOH inhibition, consistent with experiments using EtOH-naive mice. Rapid tolerance lasts 48 to 96hours, depending on whether assessing in vitro phase advances or phase delays. Similarly, in vivo, prior EtOH consumption prevented EtOH's acute blockade of photic phase delays. Finally, immunoblot experiments showed no changes in SCN glutamate receptor subunit (NR2B) expression or phosphorylation in response to rapid tolerance induction. ConclusionsThe SCN circadian clock develops rapid tolerance to EtOH as assessed both in vivo and in vitro, and the tolerance lasts for several days. These data demonstrate the utility of the circadian system as a model for investigating cellular mechanisms through which EtOH acts in the brain.
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页码:760 / 769
页数:10
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