Central nervous system effects of alcohol at a pseudo-steady-state concentration using alcohol clamping in healthy volunteers.

AIM In determining the acute effects of alcohol, it is helpful if alcohol concentrations are maintained at stable levels, to facilitate the interpretation of the results. Recently, an alcohol clamping method was developed that resulted in stable alcohol concentrations for hours. The aim of this study was to test a range of central nervous system (CNS) effects under pseudo-steady-state conditions. METHODS To achieve a pseudo-steady state of 0.6 g l(-1), breath alcohol concentrations (BrAC) were frequently measured and fed back into a spreadsheet-based program to guide intravenous dosing. CNS effects were frequently measured throughout the clamp. RESULTS The clamping paradigm resulted in a pseudo-steady-state BrAC of 0.61 g l(-1) (coefficient of variation 6.2%). A plateau was maintained from 25 to 300 min and caused significant effects on smooth pursuit eye movements [-9.7%, 95% confidence interval (CI) -12.4, -7.1], adaptive tracking (-3.4%, 95% CI -4.5, -2.2), visual analogue scale (VAS) alertness (-13 mm, 95% CI -20, -6), VAS alcohol effects (16 mm, 95% CI 7, 25) and body sway (21.3%, 95% CI 1.8, 45). Some effects (like smooth pursuit eye movements) closely followed the relatively stable alcohol concentrations, whereas others (such as body sway and VAS alcohol effects) fluctuated during the plateau phase. CONCLUSIONS Most CNS effects of alcohol showed a trend to change over time, despite stable concentrations. Other variables remained stable under pseudo-steady-state conditions. The intravenous clamping method provides precise control over BrAC levels and allows frequent repetition of different CNS measurements. These features make this technique eminently suitable to study the complex pharmacodynamic effects of acute alcohol administration.

[1]  Albert Dahan,et al.  A comparative study of two methods for attaining constant alcohol levels. , 2008, British journal of clinical pharmacology.

[2]  David J. Nutt,et al.  Blockade of alcohol's amnestic activity in humans by an α5 subtype benzodiazepine receptor inverse agonist , 2007, Neuropharmacology.

[3]  J. Gerven,et al.  Pharmacodynamic and pharmacokinetic effects of TPA023, a GABAA α2,3 subtype-selective agonist, compared to lorazepam and placebo in healthy volunteers , 2007 .

[4]  T. Otis,et al.  Ethanol acts directly on extrasynaptic subtypes of GABAA receptors to increase tonic inhibition. , 2007, Alcohol.

[5]  R. Gieschke,et al.  Pharmacodynamic interactions of diazepam and intravenous alcohol at pseudo steady state , 2005, Psychopharmacology.

[6]  E. Keskinen,et al.  Quantitative effects of ethanol infusion on smooth pursuit eye movements in man , 2004, Psychopharmacology.

[7]  A. Jones,et al.  Comparison of ethanol concentrations in venous blood and end-expired breath during a controlled drinking study. , 2003, Forensic science international.

[8]  A F Cohen,et al.  Biomarkers for the effects of benzodiazepines in healthy volunteers. , 2002, British journal of clinical pharmacology.

[9]  Sean O'Connor,et al.  Recent drinking history: association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp. , 2002, Journal of studies on alcohol.

[10]  S. Morzorati,et al.  Self-reported subjective perception of intoxication reflects family history of alcoholism when breath alcohol levels are constant. , 2002, Alcoholism, clinical and experimental research.

[11]  Ting-kai Li,et al.  Effect of Food and Food Composition on Alcohol Elimination Rates in Healthy Men and Women , 2001, Journal of clinical pharmacology.

[12]  A F Cohen,et al.  Biomarkers for the effects of antipsychotic drugs in healthy volunteers. , 2001, British journal of clinical pharmacology.

[13]  A. Hiltunen,et al.  Acute tolerance during intravenous infusion of alcohol: comparison of performance during ascending and steady state concentrations--a pilot study. , 2000, Alcohol.

[14]  D. Kareken,et al.  A preliminary study of acute responses to clamped alcohol concentration and family history of alcoholism. , 1999, Alcoholism, clinical and experimental research.

[15]  T. Li,et al.  A physiologically-based pharmacokinetic (PBPK) model for alcohol facilitates rapid BrAC clamping. , 1999, Alcoholism, clinical and experimental research.

[16]  C. Ehlers,et al.  Electroencephalographic responses to alcohol challenge in Native American Mission Indians , 1999, Biological Psychiatry.

[17]  J. Gerven,et al.  The sensitivity of pharmacodynamic tests for the central nervous system effects of drugs on the effects of sleep deprivation , 1999, Journal of psychopharmacology.

[18]  Ting-kai Li,et al.  Clamping breath alcohol concentration reduces experimental variance: application to the study of acute tolerance to alcohol and alcohol elimination rate. , 1998, Alcoholism, clinical and experimental research.

[19]  S. Kechagias,et al.  Effect of high-fat, high-protein, and high-carbohydrate meals on the pharmacokinetics of a small dose of ethanol. , 2003, British journal of clinical pharmacology.

[20]  S. Heishman,et al.  Comparative Effects of Alcohol and Marijuana on Mood, Memory, and Performance , 1997, Pharmacology Biochemistry and Behavior.

[21]  R. Gieschke,et al.  Pharmacokinetic and pharmacodynamic interactions of bretazenil and diazepam with alcohol. , 2003, British journal of clinical pharmacology.

[22]  J. Vanakoski,et al.  Lorazepam and diazepam differently impair divided attention , 1995, Pharmacology Biochemistry and Behavior.

[23]  C. Martin,et al.  Measurement of acute tolerance to alcohol in human subjects. , 1993, Alcoholism, clinical and experimental research.

[24]  H. Schoemaker,et al.  A comparison of the sensitivities of adaptive tracking, eye movement analysis, and visual analog lines to the effects of incremental doses of temazepam in healthy volunteers , 1991, Clinical pharmacology and therapeutics.

[25]  Effect of haloperidol on a symbol digit substitution task in normal adult males. , 1989, Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology.

[26]  J. Hayward,et al.  Effect of hyperthermia on breath-alcohol analysis. , 1987, Journal of forensic sciences.

[27]  W. Neuteboom,et al.  The effects of hypo- and hyperventilation on breath alcohol measurements. , 1987, Blutalkohol.

[28]  J. Hayward,et al.  Effect of hypothermia on breath-alcohol analysis. , 1987, Journal of forensic sciences.

[29]  A. Cohen,et al.  Lamotrigine (BW430C), a potential anticonvulsant. Effects on the central nervous system in comparison with phenytoin and diazepam. , 1985, British journal of clinical pharmacology.

[30]  C. Naranjo,et al.  Is there acute tolerance to alcohol at steady state? , 1985, Journal of studies on alcohol.

[31]  R G Borland,et al.  Visual motor co-ordination and dynamic visual acuity. , 1984, British journal of clinical pharmacology.

[32]  A. T. Smith,et al.  Benzodiazepines impair smooth pursuit eye movements. , 1983, British journal of clinical pharmacology.

[33]  A. Jones,et al.  How Breathing Technique Can Influence the Results of Breath-Alcohol Analysis , 1982, Medicine, science, and the law.

[34]  P. Wilkinson,et al.  Pharmacokinetics of ethanol: a review. , 1980, Alcoholism, clinical and experimental research.

[35]  R. Baloh,et al.  Quantitative measurement of saccade amplitude, duration, and velocity , 1975, Neurology.

[36]  A. Bond,et al.  The use of analogue scales in rating subjective feelings , 1974 .

[37]  Wright Bm A simple mechanical ataxia-meter. , 1971 .

[38]  H. Norris The action of sedatives on brain stem oculomotor systems in man. , 1971, Neuropharmacology.

[39]  B. M. Wright A simple mechanical ataxia-meter. , 1971, The Journal of physiology.