首页> 美国卫生研究院文献>other >BRIEF CONSTANT LIGHT ACCELERATES SEROTONERGIC RE-ENTRAINMENT TO LARGE SHIFTS OF THE DAILY LIGHT-DARK CYCLE
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BRIEF CONSTANT LIGHT ACCELERATES SEROTONERGIC RE-ENTRAINMENT TO LARGE SHIFTS OF THE DAILY LIGHT-DARK CYCLE

机译:短暂的恒定光加速了每日轻黑暗周期大位移的5-羟色胺再吸收

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摘要

Brief (~2 day) constant light exposure (LLb) in hamsters dramatically enhances circadian phase-resetting induced by the serotonin (5-HT) receptor agonist, 8-OH-DPAT and other nonphotic stimuli. The present study was undertaken to determine if LLb can also amplify phase-resetting responses to endogenous 5-HT and accelerate re-entrainment to large-magnitude advance and delay shifts of the light-dark (LD) cycle. First, central serotonergic activity was increased by i.p. injection of L-tryptophan +/− the 5-HT reuptake inhibitor fluoxetine. Hamsters under LD or exposed to LLb received vehicle or drugs during the early morning, and phase-shifts of the locomotor activity rhythm were measured after release to constant darkness. Neither drug phase-shifted animals not exposed to LLb (p>0.5 vs. vehicle); however in animals receiving LLb, L-tryptophan with and without fluoxetine produced large phase-advance shifts (means=2.5±0.4h and 2.6±0.2h, respectively; both p<0.035 vs. vehicle). Next, the effects of LLb combined with 8-OH-DPAT or L-tryptophan+fluoxetine on serotonergic re-entrainment to 10 h phase-advance and phase-delay shifts of the LD cycle were assessed. In groups not exposed to LLb, vehicle controls re-entrained slowly to the advance and delay shifts (means=16±1 days and 24±4 days, respectively), but those treated with 8-OH-DPAT re-entrained faster (means=11±2 days and 9±2 days, respectively; both p<0.05 vs. vehicle). In groups exposed to LLb, vehicle controls re-entrained slowly to the advance and delay shifts (means=15±2 and 25±3 days, respectively); however those receiving 8-OH-DPAT rapidly re-entrained to the delay and advance shifts, with the majority (75%) requiring only 1–2 days (means=2±1 days and 4±2 days, respectively; both p<0.05 vs. vehicle). Animals exposed to LLb and treated with L-tryptophan+fluoxetine also exhibited accelerated re-entrainment to a 10 h advance shift (mean=5±2days; p<0.05 vs. vehicle). Thus through enhancing serotonergic phase-resetting, LLb facilitates rapid re-entrainment to large shifts of the LD cycle which offers a potential approach for treating circadian-related desynchronies.
机译:仓鼠中短暂的(约2天)持续光照(LLb)大大增强了由血清素(5-HT)受体激动剂,8-OH-DPAT和其他非光刺激引起的昼夜节律复位。进行本研究以确定LLb是否还可以放大对内源5-HT的相位重置响应,并加速重夹带至大幅度超前和明暗(LD)周期的延迟移位。首先,腹腔内5-羟色胺能活动增加。注射L-色氨酸+/- 5-羟色胺再摄取抑制剂氟西汀。在清晨,处于LD下或暴露于LLb的仓鼠接受了媒介物或药物,在释放到恒定的黑暗中后,测量了运动活动节奏的相移。药物相移的动物均未暴露于LLb(与媒介物相比,p> 0.5);然而,在接受LLb的动物中,有和没有氟西汀的L-色氨酸产生较大的相移(均值分别为2.5±0.4h和2.6±0.2h;相对于赋形剂,均p <0.035)。接下来,评估了LLb与8-OH-DPAT或L-色氨酸+氟西汀组合对5-羟色胺能再夹带至10 h相位提前和LD周期的相位延迟位移的影响。在未暴露于LLb的组中,媒介物对照缓慢地重新夹带至提前和延迟班次(分别为16±1天和24±4天),但用8-OH-DPAT治疗的对照则较快地夹带(均值分别为11±2天和9±2天;与媒介物相比,均p <0.05)。在暴露于LLb的组中,媒介物对照缓慢地重新夹带至提前和延迟移位(分别为15±2天和25±3天);然而,接受8-OH-DPAT的患者迅速重新陷入延迟和提前转变,大多数(75%)仅需要1-2天(分别意味着2±1天和4±2天;两者均p < 0.05对车辆)。暴露于LLb并用L-色氨酸+氟西汀治疗的动物也表现出加速的再夹带,提前了10小时(平均= 5±2天;相对于媒介物,p <0.05)。因此,通过增强5-羟色胺能的相位重置,LLb有助于快速重新夹带至LD周期的大移位,这为治疗昼夜节律相关的失调提供了一种可能的方法。

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