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Serotonin1A-mediated amplification of light-induced phase advances of circadian rhythms in the Syrian hamster: post-light effects.

机译:血清素1A介导的叙利亚仓鼠昼夜节律的光诱导相进展的光放大:后光效应。

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Certain serotonergic compounds that have an agonist/antagonist activity at the 5-HT(1A) receptor subtype are known to greatly potentiate the ability of light to advance the phase of circadian activity rhythms in hamsters. Typically, investigational compounds are injected 30 min to 1 h prior to a phase-advancing light pulse, and it is not known if these compounds are efficacious when injected after a short light pulse. In this study we injected the 5-HT(1A) mixed agonist/antagonist BMY 7378 from 1 to 7 h after a short phase advancing light pulse at CT 19 in hamsters to assess the temporal window of efficacy of this compound. BMY 7378 effectively doubles the magnitude of light-induced phase advances in hamster circadian wheel running rhythms for 6 h after a light pulse administered at CT 19, and this effect abruptly ends at 7 h post-light. This demonstrates that the molecular events initiated by a light pulse at CT 19 responsible for initiating phase advances in circadian activity rhythms can be modulated for at least the next 6 h in the hamster. However, this effect found with BMY 7378 does not extend to all serotonergic compounds as the inhibitory activity of 8-OH-DPAT on light-induced phase advances is not apparent when injected just 3 h after a light pulse. Since BMY 7378 can elicit such major shifts in the timing of the circadian clock it should be useful as a tool to explore potential changes in gene expression that lead to phase shifts in circadian rhythms, now known to be susceptible to modification for 6 h after a phase-advancing light pulse.
机译:已知对5-HT(1A)受体亚型具有激动/拮抗活性的某些血清素能化合物可大大增强光使仓鼠昼夜节律活动期发展的能力。通常,在相位超前的光脉冲之前30分钟至1小时注射待研究的化合物,尚不清楚在短光脉冲后注射这些化合物是否有效。在这项研究中,我们在仓鼠中在CT 19处短时间推进光脉冲后1至7小时注射了5-HT(1A)混合激动剂/拮抗剂BMY 7378,以评估该化合物功效的时间窗。 BMY 7378在CT 19处施加光脉冲后6个小时内,使仓鼠生物钟运行节奏中的光诱导相位超前的幅度增加了一倍,并且这种影响在光照后7个小时突然终止。这表明,由CT 19处的光脉冲引发的分子事件,可引起昼夜节律活动节律的阶段提前,至少在接下来的6 h内可对其进行调制。但是,BMY 7378所发现的这种作用并未扩展到所有血清素能化合物,因为在光脉冲后仅3 h注射时8-OH-DPAT对光诱导相的抑制活性并不明显。由于BMY 7378可以引起昼夜节律时钟的这种重大变化,因此它应作为探索基因表达的潜在变化的工具,该变化可能导致昼夜节律的相移,目前已知该变化易于在昼夜节律后6小时内发生。相位超前的光脉冲。

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