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在长期使用氯吉兰和锂治疗期间,光诱导途径对光的敏感性降低。

Decreased sensitivity to light of the photic entrainment pathway during chronic clorgyline and lithium treatments.

作者信息

Duncan W C, Johnson K A, Wehr T A

机构信息

Section on Biological Rhythms, National Institute of Mental Health, Bethesda, MD 20892, USA.

出版信息

J Biol Rhythms. 1998 Aug;13(4):330-46. doi: 10.1177/074873098129000165.

Abstract

Certain antidepressant drugs (ADs) cause disturbances in sleep that could result from their capacity to alter the timing of circadian rhythms. Effects on the timing of rhythms could be due to the drugs' known capacity to alter the frequency of the intrinsic rhythm of the circadian pacemaker, or to a capacity to modify the pacemaker's response to external stimuli that serve as time cues (Zeitgebers) that regulate the timing (phase) of its rhythm. To examine the possibility that ADs alter the sensitivity of the system that mediates the phase-shifting effects of light, hamsters were treated chronically with the MAOI, clorgyline, and lithium. Each hamster was then exposed to a single 5-min light pulse (intensity range = 0.00137 to 137 microW/cm2) at circadian phases known to elicit phase advances (CT18) and phase delays (CT13.5) in the daily onset of wheel running. The half-saturation constant (sigma), photic sensitivity (1/sigma), and maximum phase-shifting response to light were estimated from the best-fit stimulus response curves. In addition, threshold sensitivity, the light intensity required to produce a threshold phase-shifting response, was determined. Clorgyline decreased the magnitude of light-induced phase advances at each of the light intensities tested. Clorgyline also decreased the magnitude of light-induced phase delays at low light intensities, but increased the magnitude of phase delays at higher light intensities. Clorgyline decreased the sensitivity of the photic phase-shifting system, as indicated both by the threshold sensitivities at CT13.5 and CT18, and by 1/sigma at CT13.5. Lithium decreased the threshold sensitivity at CT18, and 1/sigma at CT13.5. Lithium decreased the magnitude of phase delays, but not phase advances. Clorgyline's effects on the photic entrainment pathway may be mediated by its effects on serotonin, which has been shown to modulate the pacemaker's response to morning and evening light, and by tolerance to this effect of serotonin. The fact that both clorgyline and lithium decrease the photic sensitivity of the entrainment pathway suggests that other psychoactive drugs might also share this property. It is possible that the decreased sensitivity to light of the entrainment pathway affects the clinical response to these and other psychoactive medications.

摘要

某些抗抑郁药物(ADs)会导致睡眠障碍,这可能源于它们改变昼夜节律时间的能力。对节律时间的影响可能是由于药物已知的改变昼夜节律起搏器固有节律频率的能力,或者是由于改变起搏器对作为调节其节律时间(相位)的时间线索(授时因子)的外部刺激的反应的能力。为了研究抗抑郁药物是否会改变介导光的相位移动效应的系统的敏感性,将仓鼠长期用单胺氧化酶抑制剂氯吉兰和锂进行治疗。然后,在已知会引起日常转轮活动起始的相位提前(CT18)和相位延迟(CT13.5)的昼夜节律阶段,让每只仓鼠暴露于单个5分钟的光脉冲(强度范围 = 0.00137至137微瓦/平方厘米)。根据最佳拟合刺激反应曲线估计半饱和常数(sigma)、光敏感性(1/sigma)以及对光的最大相位移动反应。此外,还确定了产生阈值相位移动反应所需的光强度,即阈值敏感性。氯吉兰在每个测试的光强度下都降低了光诱导的相位提前幅度。氯吉兰在低光强度下也降低了光诱导的相位延迟幅度,但在较高光强度下增加了相位延迟幅度。氯吉兰降低了光相位移动系统的敏感性,这在CT13.5和CT18处的阈值敏感性以及CT13.5处的1/sigma中均有体现。锂降低了CT18处的阈值敏感性以及CT13.5处的1/sigma。锂降低了相位延迟的幅度,但没有降低相位提前的幅度。氯吉兰对光诱导途径的影响可能是由其对血清素的影响介导的,血清素已被证明可调节起搏器对早晨和傍晚光线的反应,以及对血清素这种作用的耐受性。氯吉兰和锂都降低了诱导途径的光敏感性这一事实表明,其他精神活性药物可能也具有这种特性。诱导途径对光的敏感性降低可能会影响对这些和其他精神活性药物的临床反应。

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