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色氨酸负荷调节哺乳动物昼夜节律系统中的光诱导反应。

Tryptophan loading modulates light-induced responses in the mammalian circadian system.

作者信息

Glass J D, Selim M, Srkalovic G, Rea M A

机构信息

Department of Biological Sciences, Kent State University, OH 44242, USA.

出版信息

J Biol Rhythms. 1995 Mar;10(1):80-90. doi: 10.1177/074873049501000107.

Abstract

Enhanced endogenous serotonergic activity, stimulated by L-tryptophan (TRYPT) loading, was found to have a substantial impact on neurochemical and behavioral aspects of the circadian response to light in the male Syrian hamster. An intraperitoneal (i.p.) injection of 150 mg/kg TRYPT significantly stimulated serotonin (5-HT) release in the suprachiasmatic nuclear (SCN) region, as reflected by a 205 +/- 30% maximal increase in the extracellular concentration of 5-HT assessed using microdialysis. Administration of TRYPT 1 h before exposure to a light pulse (30 min, 40 lux) delivered during late subjective night dose-dependently suppressed the number of SCN cells expressing light-induced Fos-like immunoreactivity (Fos-LI; maximal suppression @200 mg/kg was 77 +/- 4%, p < 0.001). This action of TRYPT was attenuated by pretreatment with the 5-HT1a antagonist, NAN-190, and was abolished by the 5-HT2/5-HT7 antagonist, ritanserin, or the nonselective 5-HT antagonist, metergoline (all 10 mg/kg). These antagonists alone had no effect on light-induced Fos. In a second experiment, pretreatment of free-running hamsters housed under constant darkness with 150 mg/kg TRYPT 45-60 min prior to light exposure (10 min, 20 lux) during late subjective night (CT 19) significantly attenuated the light-induced phase advances of the circadian activity rhythm (66 +/- 7 min vs. 100 +/- 6 min for vehicle controls; p < 0.001). The same dose of TRYPT given 1 h before lights-on for 5 consecutive days in hamsters maintained under 14L:10D altered the phase angle of entrainment such that activity onsets were delayed by 36 +/- 8 min relative to controls (p < 0.05). The same dose of TRYPT administered during late subjective night also suppressed the extracellular concentration of glutamate in the SCN region assessed using microdialysis (55 +/- 8% suppression; p < 0.05 vs. baseline). These results support the hypothesis that the ascending serotonergic projection to the SCN modulates photic entrainment processes within the circadian oscillator.

摘要

研究发现,L-色氨酸(TRYPT)负荷刺激增强的内源性血清素能活性,对雄性叙利亚仓鼠昼夜节律对光的神经化学和行为方面有重大影响。腹腔注射150mg/kg TRYPT可显著刺激视交叉上核(SCN)区域的血清素(5-HT)释放,使用微透析评估细胞外5-HT浓度最大增加205±30%可反映这一点。在主观夜间晚期给予光脉冲(30分钟,40勒克斯)前1小时给予TRYPT,剂量依赖性地抑制表达光诱导Fos样免疫反应性(Fos-LI)的SCN细胞数量(200mg/kg时最大抑制率为77±4%,p<0.001)。TRYPT的这种作用被5-HT1a拮抗剂NAN-190预处理减弱,被5-HT2/5-HT7拮抗剂利坦色林或非选择性5-HT拮抗剂麦角林(均为10mg/kg)消除。这些拮抗剂单独对光诱导的Fos无影响。在第二个实验中,在主观夜间晚期(CT 19)光照(10分钟,20勒克斯)前45-60分钟,给处于持续黑暗中的自由活动仓鼠预处理150mg/kg TRYPT,显著减弱了昼夜活动节律的光诱导相位提前(与溶剂对照组相比为66±7分钟对100±6分钟;p<0.001)。在14L:10D条件下饲养的仓鼠中,连续5天在开灯前1小时给予相同剂量的TRYPT,改变了同步化的相位角,使得活动开始时间相对于对照组延迟了36±8分钟(p<0.05)。在主观夜间晚期给予相同剂量的TRYPT,也抑制了使用微透析评估的SCN区域谷氨酸的细胞外浓度(抑制率为55±8%;与基线相比p<0.05)。这些结果支持这样的假设,即向SCN的上行血清素能投射调节昼夜节律振荡器内的光同步化过程。

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