Hou R H, Samuels E R, Langley R W, Szabadi E, Bradshaw C M
Psychopharmacology Section, Division of Psychiatry, University of Nottingham, Medical School Room B109, Queen's Medical Centre, Nottingham, UK.
Psychopharmacology (Berl). 2007 Nov;195(1):41-59. doi: 10.1007/s00213-007-0884-y. Epub 2007 Jul 22.
There is a close relationship between arousal and pupil diameter, decrease in the level of arousal being accompanied by constriction of the pupil (miosis), probably reflecting the attenuation of sympathetic outflow as sedation sets in. Paradoxically, sedation induced by benzodiazepines is not accompanied by miosis.
The objective of this study was to examine the hypothesis that diazepam may attenuate both the sympathetic and the opposing parasympathetic outflow to the iris, which may mask the miosis. Dapiprazole (sympatholytic) and tropicamide (parasympatholytic) were applied topically, together with the cold pressor test (CPT), to manipulate the sympathetic/parasympathetic balance.
Sixteen healthy male volunteers participated in four weekly sessions according to a balanced double-blind protocol. Diazepam 10 mg (two sessions) and placebo (two sessions), associated with either 0.01% tropicamide or 0.5% dapiprazole eyedrops, were administered orally. Pupil diameter, light and darkness reflexes and pupillary sleepiness waves were recorded with infrared video pupillometry, alertness was measured by critical flicker fusion frequency (CFFF) and visual analogue scales (VAS), blood pressure and heart rate by conventional methods. CPT was applied after post-treatment testing. Data were analysed by analysis of variance, with multiple comparisons.
Diazepam caused sedation (reduction in VAS alertness scores and CFFF, increase in sleepiness waves), dapiprazole had a sympatholytic and tropicamide a parasympatholytic effect on the pupil. Diazepam had no effect on pupil diameter and reflexes or their modifications by the antagonists. CPT increased pupil diameter, blood pressure and heart rate, and the increase only in systolic blood pressure was attenuated by diazepam.
Diazepam-induced sedation is not accompanied by any change in either the sympathetic or parasympathetic influence on the iris.
觉醒与瞳孔直径之间存在密切关系,觉醒水平降低伴随着瞳孔收缩(瞳孔缩小),这可能反映出随着镇静作用的出现交感神经输出减弱。矛盾的是,苯二氮䓬类药物诱导的镇静并不伴有瞳孔缩小。
本研究的目的是检验以下假设:地西泮可能会减弱交感神经和与之相反的副交感神经向虹膜的输出,这可能掩盖瞳孔缩小。局部应用达哌唑(抗交感神经药)和托吡卡胺(抗副交感神经药),并结合冷加压试验(CPT)来调节交感神经/副交感神经平衡。
16名健康男性志愿者按照平衡双盲方案参加了为期四周的四个阶段试验。口服10mg地西泮(两个阶段)和安慰剂(两个阶段),同时使用0.01%托吡卡胺或0.5%达哌唑眼药水。用红外视频瞳孔测量法记录瞳孔直径、光反射和暗反射以及瞳孔困倦波,用临界闪烁融合频率(CFFF)和视觉模拟量表(VAS)测量警觉性,用传统方法测量血压和心率。在治疗后测试后进行CPT。数据采用方差分析和多重比较进行分析。
地西泮引起镇静(VAS警觉性评分降低和CFFF降低,困倦波增加),达哌唑对瞳孔有抗交感神经作用,托吡卡胺有抗副交感神经作用。地西泮对瞳孔直径、反射或拮抗剂对其的改变没有影响。CPT使瞳孔直径、血压和心率增加,而地西泮仅减弱了收缩压的升高。
地西泮诱导的镇静不会伴随交感神经或副交感神经对虹膜的影响发生任何变化。