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Arousal and the pupil: why diazepam-induced sedation is not accompanied by miosis

Arousal and the pupil: why diazepam-induced sedation is not accompanied by miosis
Arousal and the pupil: why diazepam-induced sedation is not accompanied by miosis
Rationale 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.
Objective 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.
Materials and methods 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.
Results 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.
Conclusions Diazepam-induced sedation is not accompanied by any change in either the sympathetic or parasympathetic influence on the iris.
drug effects, psychiatry, pupillary, blood pressure, miosis, heart rate, physiopathology, etiology, flicker fusion, cold, cardiovascular physiology, cross-over studies, administration & dosage
0033-3158
41-59
Hou, R.H.
470bdcbc-93a9-4dad-aac5-26d455c34376
Samuels, E.R.
be1fd344-e73a-43da-aca8-33c6e21cb7f2
Langley, R.W.
579cc42e-972f-4422-952f-1c76ecc4b4e3
Szabadi, E.
cff688f8-264f-4ca3-a2c4-cb10930f1956
Bradshaw, C.M.
0baafd10-0e91-4113-b90b-27132bd77305
Hou, R.H.
470bdcbc-93a9-4dad-aac5-26d455c34376
Samuels, E.R.
be1fd344-e73a-43da-aca8-33c6e21cb7f2
Langley, R.W.
579cc42e-972f-4422-952f-1c76ecc4b4e3
Szabadi, E.
cff688f8-264f-4ca3-a2c4-cb10930f1956
Bradshaw, C.M.
0baafd10-0e91-4113-b90b-27132bd77305

Hou, R.H., Samuels, E.R., Langley, R.W., Szabadi, E. and Bradshaw, C.M. (2007) Arousal and the pupil: why diazepam-induced sedation is not accompanied by miosis. Psychopharmacology, 195 (1), 41-59. (doi:10.1007/s00213-007-0884-y).

Record type: Article

Abstract

Rationale 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.
Objective 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.
Materials and methods 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.
Results 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.
Conclusions Diazepam-induced sedation is not accompanied by any change in either the sympathetic or parasympathetic influence on the iris.

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More information

Published date: November 2007
Keywords: drug effects, psychiatry, pupillary, blood pressure, miosis, heart rate, physiopathology, etiology, flicker fusion, cold, cardiovascular physiology, cross-over studies, administration & dosage
Organisations: Clinical Neurosciences

Identifiers

Local EPrints ID: 73589
URI: http://eprints.soton.ac.uk/id/eprint/73589
ISSN: 0033-3158
PURE UUID: acbb4fe8-b7d8-4f98-a97d-07bd4db6c406
ORCID for R.H. Hou: ORCID iD orcid.org/0000-0001-6127-1478

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Date deposited: 15 Mar 2010
Last modified: 14 Mar 2024 02:52

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Contributors

Author: R.H. Hou ORCID iD
Author: E.R. Samuels
Author: R.W. Langley
Author: E. Szabadi
Author: C.M. Bradshaw

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