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1.
Eur Neuropsychopharmacol ; 22(7): 492-500, 2012 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-22209365

RESUMO

While a number of behavioural studies have been conducted to investigate the acute effects of amphetamines on tasks of attention and information processing, there is currently a scarcity of research concerning their electrophysiological effects in healthy adults. It is also unclear as to whether amphetamines exert effects on stimulus evaluation or response selection. In two studies, independent groups of twenty healthy illicit stimulant users aged between 21 and 32 years were administered 0.42 mg/kg d-amphetamine versus placebo, and 0.42 mg/kg d-methamphetamine versus placebo respectively, and completed an auditory oddball task on two separate testing days. A 62-channel EEG was recorded during the completion of the task, and the effects of amphetamines on N200 and P300 ERP components were analysed. d-amphetamine significantly decreased reaction time, improved accuracy, and reduced the latency of the P300 component relative to placebo, while having no effect on the N200 component. d-methamphetamine had no effect on reaction time, accuracy or the P300 component, but reduced the amplitude of the N200 component, relative to placebo. It was concluded that there is tentative support to suggest that d-amphetamine at a dose of 0.42 mg/kg may enhance speed of information processing while d-methamphetamine at a dose of 0.42 mg/kg may reflect changes to stimulus evaluation.


Assuntos
Ondas Encefálicas/efeitos dos fármacos , Estimulantes do Sistema Nervoso Central/farmacologia , Dextroanfetamina/farmacologia , Potenciais Evocados/efeitos dos fármacos , Metanfetamina/farmacologia , Estimulação Acústica , Adulto , Análise de Variância , Relação Dose-Resposta a Droga , Eletroencefalografia , Feminino , Humanos , Masculino , Testes Neuropsicológicos , Tempo de Reação/efeitos dos fármacos , Adulto Jovem
2.
Forensic Sci Int ; 155(2-3): 172-8, 2005 Dec 20.
Artigo em Inglês | MEDLINE | ID: mdl-16226154

RESUMO

The consumption of Delta9-tetrahydrocannabinol (THC) as cannabis has been shown to result in impaired and culpable driving. Testing drivers for the presence of THC in blood is problematic as THC and its metabolites may remain in the blood for several days following its consumption, even though the drug may no longer have an influence on driving performance. In the present study, the aim was to assess whether performance on the standardised field sobriety tests (SFSTs) provides a sensitive measure of impaired driving behaviour following the consumption of THC. In a repeated measures design, 40 participants consumed cigarettes that contained either 0% THC (placebo), 1.74% THC (low dose) or 2.93% THC (high dose). For each condition, after smoking a cigarette, participants performed the SFSTs on three occasions (5, 55 and 105 min after the smoking procedure had been completed) as well as a simulated driving test on two occasions (30 and 80 min after the smoking procedure had been completed). The results revealed that driving performance was not significantly impaired 30 min after the consumption of THC but was significantly impaired 80 min after the consumption of THC in both the low and high dose conditions. The percentage of participants whose driving performance was correctly classified as either impaired or not impaired based on the SFSTs ranged between 65.8 and 76.3%, across the two THC conditions. The results suggest that performance on the SFSTs provides a moderate predictor of driving impairment following the consumption of THC and as such, the SFSTs may provide an appropriate screening tool for authorities that wish to assess the driving capabilities of individuals suspected of being under the influence of a drug other than alcohol.


Assuntos
Exame para Habilitação de Motoristas , Dronabinol/sangue , Abuso de Maconha/sangue , Psicotrópicos/sangue , Detecção do Abuso de Substâncias/métodos , Adulto , Condução de Veículo , Simulação por Computador , Dronabinol/administração & dosagem , Feminino , Medicina Legal , Cromatografia Gasosa-Espectrometria de Massas , Humanos , Masculino , Abuso de Maconha/diagnóstico , Psicotrópicos/administração & dosagem , Fatores de Tempo
3.
Psychopharmacology (Berl) ; 179(3): 536-43, 2005 May.
Artigo em Inglês | MEDLINE | ID: mdl-15614573

RESUMO

RATIONALE: The number of road fatalities related to the presence of amphetamines in drivers has been relatively constant over the past 10 years. However, there remains uncertainty as to the extent that these drugs induce driving impairment, and whether any such impairments translate to an increase in road fatalities. OBJECTIVES: To examine the acute effects of 0.42 mg/kg dexamphetamine on simulated driving performance, and to establish which, if any, simulated driving abilities become impaired following dexamphetamine administration. METHODS: A repeated-measures, counter-balanced, double-blind, placebo-controlled design was employed. Twenty healthy volunteers completed two treatment conditions-0.42 mg/kg dexamphetamine and placebo. Performance was assessed using a driving simulator task. Blood and saliva samples were obtained prior to the driving tasks and immediately after task completion (120 min and 170 min post-drug administration, respectively). RESULTS: Mean dexamphetamine blood concentrations were 83 ng/ml and 98 ng/ml at 120 min and 170 min, respectively. Results indicated a decrease in overall simulated driving ability following dexamphetamine administration during the day-time but not the night-time scenario tasks. Contributing to this performance reduction, "incorrect signalling", "failing to stop at a red traffic light" and "slow reaction times" were the behaviours most strongly affected by dexamphetamine. CONCLUSIONS: The decrease in simulated driving ability observed during the day-time driving tasks are consistent with the perceptual narrowing or tunnel vision that is associated with dexamphetamine consumption.


Assuntos
Condução de Veículo , Simulação por Computador , Dextroanfetamina/farmacologia , Desempenho Psicomotor/efeitos dos fármacos , Adulto , Método Duplo-Cego , Feminino , Humanos , Masculino , Desempenho Psicomotor/fisiologia
4.
Psychopharmacology (Berl) ; 180(1): 107-14, 2005 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-15619106

RESUMO

The Standardised Field Sobriety Tests (SFST) were developed to test for alcohol intoxication but are currently being used by the State Police of Victoria (Australia) to test for driving impairment associated with drugs other than alcohol. The aim of the present study was to assess whether the SFSTs provide a sensitive measure of impairment following the consumption of a drug other than alcohol: delta-9-tetrahydrocannabinol (THC or cannabis). In a repeated-measures design, 40 participants consumed cigarettes that contained either 0% THC (placebo), 1.74% THC (low dose) or 2.93% THC (high dose). For each condition, after smoking a cigarette, participants performed the SFSTs on three occasions: 5 min (Time 1), 55 min (Time 2) and 105 min (Time 3) after the smoking procedure had been completed. The results revealed that there was a positive relationship between the dose of THC administered and the number of participants classified as impaired based on the SFSTs. Results also revealed that the percentage of participants classified as impaired decreased from Time 1 to Time 3 and that the addition of a new sign, head movements or jerks (HMJ), increased the percentage of participants classified as impaired in both the low and high THC conditions. These findings suggest that impaired performance on the SFSTs is positively related to the dose of THC administered and that the inclusion of HMJ as a scored sign in the SFSTs improves their predictive validity when testing for THC intoxication.


Assuntos
Dronabinol/efeitos adversos , Abuso de Maconha , Desempenho Psicomotor/efeitos dos fármacos , Adulto , Relação Dose-Resposta a Droga , Feminino , Humanos , Masculino , Valor Preditivo dos Testes
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