Does a Medicinal Dose of Kava Impair Driving? A Randomized, Placebo-Controlled, Double-Blind Study

被引:8
作者
Sarris, J. [1 ,2 ,3 ]
Laporte, E. [2 ,3 ]
Scholey, A. [2 ,3 ]
King, R. [2 ,3 ]
Pipingas, A. [2 ,3 ]
Schweitzer, I. [1 ]
Stough, C. [2 ,3 ]
机构
[1] Univ Melbourne, Dept Psychiat, Melbourne, Vic, Australia
[2] Swinburne Univ Technol, Ctr Human Psychopharmacol, Melbourne, Vic, Australia
[3] NICM Collaborat Ctr Neurocognit, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
driving; driving safety; kava; oxazepam; cognition; EVENT-RELATED POTENTIALS; PIPER-METHYSTICUM; ENRICHED EXTRACT; NA+-CHANNELS; BINDING-SITE; OXAZEPAM; PERFORMANCE; INHIBITION; DIAZEPAM; ALCOHOL;
D O I
10.1080/15389588.2012.682233
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Overview: Increasing concerns over the potentially impairing effects of prescriptive sedative drugs such as benzodiazepines on driving have been raised. However, other alternatives such as natural medicines may also carry similar risks with respect to driving safety. Kava (Piper methysticum) is a psychotropic plant commonly used both recreationally and medicinally in the United States, Australia, and the South Pacific to elicit a physically tranquilizing effect. To date no controlled study has tested a medicinal dose of kava versus placebo and a standard sedative drug on driving ability and driving safety. Objective: Due to the need to establish the safety of kava in operating a motor vehicle, we compared the acute effects of the plant extract versus the benzodiazepine oxazepam and placebo using a driving simulator. Methods: A driving simulator (AusEd) was used by 22 adults aged between 18 and 65years after being randomly administered an acute medicinal dose of kava (180mg of kavalactones), oxazepam (30mg), or placebo one week apart in a crossover design trial. Results: No impairing effects on driving outcomes were found after kava administration compared to placebo. Results on specific driving outcome domains revealed that the oxazepam condition had significantly slower braking reaction time compared to the placebo condition (p =.002) and the kava condition (p =.003). The kava condition had significantly fewer lapses of concentration compared to the oxazepam condition (p =.033). No significant differences were found between conditions for steering deviation, speed deviation, and number of crashes. Results were not modified by driving experience. On the Bond-Lader visual analogue sub-scale of alertness, a significant Treatment x Time interaction (p =.032) was found, with a significant reduction over time for oxazepam decreasing alertness (p <.001), whereas no significant reduction was found in the kava or placebo conditions. Conclusion: The results indicate that a medicinal dose of kava containing 180mg of kavalactones does not impair driving ability, whereas 30mg of oxazepam shows some impairment. Research assessing larger recreational doses of kava on driving ability should now be conducted.
引用
收藏
页码:13 / 17
页数:5
相关论文
共 31 条
[1]   Effect of kava extract and individual kavapyrones on neurotransmitter levels in the nucleus accumbens of rats [J].
Baum, SS ;
Hill, R ;
Rommelspacher, H .
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 1998, 22 (07) :1105-1120
[2]   STUDIES OF CLOBAZAM AND CAR-DRIVING [J].
BIEHL, B .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1979, 7 :S85-S90
[3]   USE OF ANALOG SCALES IN RATING SUBJECTIVE FEELINGS [J].
BOND, A ;
LADER, M .
BRITISH JOURNAL OF MEDICAL PSYCHOLOGY, 1974, 47 (SEP) :211-218
[4]   Influence of genuine kavapyrone enantiomers on the GABAA binding site [J].
Boonen, G ;
Haberlein, H .
PLANTA MEDICA, 1998, 64 (06) :504-506
[5]   A further examination of the time-dependent effects of oxazepam and lorazepam on implicit and explicit memory [J].
Buffett-Jerrott, SE ;
Stewart, SH ;
Teehan, MD .
PSYCHOPHARMACOLOGY, 1998, 138 (3-4) :344-353
[6]   The utility of the AusEd driving simulator in the clinical assessment of driver fatigue [J].
Desai, Anup V. ;
Wilsmore, Brad ;
Bartlett, Delwyn J. ;
Unger, Gunnar ;
Constable, Ben ;
Joffe, David ;
Grunstein, Ronald R. .
BEHAVIOR RESEARCH METHODS, 2007, 39 (03) :673-681
[7]   Kavain inhibits non-stereospecifically veratridine-activated Na+ channels [J].
Gleitz, J ;
Gottner, N ;
Ameri, A ;
Peters, T .
PLANTA MEDICA, 1996, 62 (06) :580-581
[8]   THE ASSESSMENT OF ANXIETY-STATES BY RATING [J].
HAMILTON, M .
BRITISH JOURNAL OF MEDICAL PSYCHOLOGY, 1959, 32 (01) :50-55
[9]   PHARMACOPSYCHOLOGICAL EFFECTS OF OXAZEPAM AND KAVA-EXTRACT IN A VISUAL-SEARCH PARADIGM ASSESSED WITH EVENT-RELATED POTENTIALS [J].
HEINZE, HJ ;
MUNTHE, TF ;
STEITZ, J ;
MATZKE, M .
PHARMACOPSYCHIATRY, 1994, 27 (06) :224-230
[10]  
Herberg KW, 1991, Z ALLGEMEINMED, V13, P842