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1.
The present work investigated the effects of caffeine (0 mg, 100 mg, 200 mg, 400 mg) on a flanker task designed to test Posner’s three visual attention network functions: alerting, orienting, and executive control [Posner, M. I. (2004). Cognitive neuroscience of attention. New York, NY: Guilford Press]. In a placebo-controlled, double-blind study using a repeated-measures design, we found that the effects of caffeine on visual attention vary as a function of dose and the attention network under examination. Caffeine improved alerting and executive control function in a dose–response manner, asymptoting at 200 mg; this effect is congruent with caffeine’s adenosine-mediated effects on dopamine-rich areas of brain, and the involvement of these areas in alerting and the executive control of visual attention. Higher doses of caffeine also led to a marginally less efficient allocation of visual attention towards cued regions during task performance (i.e., orienting). Taken together, results of this study demonstrate that caffeine has differential effects on visual attention networks as a function of dose, and such effects have implications for hypothesized interactions of caffeine, adenosine and dopamine in brain areas mediating visual attention.  相似文献   
2.
Recent work suggests that a dose of 200–400 mg caffeine can enhance both vigilance and the executive control of visual attention in individuals with low caffeine consumption profiles. The present study seeks to determine whether individuals with relatively high caffeine consumption profiles would show similar advantages. To this end, we examined the effects of four caffeine doses (0 mg, 100 mg, 200 mg, 400 mg) on low- and high-level visual attention in individuals with high consumption profiles (n = 36), in a double-blind study using a repeated measures design. Results from the Attention Network Test indicated that caffeine enhanced both vigilance and the executive control of visual attention, but only at the highest administered dose (400 mg). We demonstrate that in habitual consumers high doses of caffeine can produce beneficial changes in visual attention. These results carry implications for the theorized interactions between caffeine, adenosine and dopamine in brain regions mediating visual attention.  相似文献   
3.
The study examined the role of caffeine consumption in caffeine reinforcement. Previous findings have shown that caffeine reinforced flavor preference in moderate caffeine consumers who are caffeine deprived. However, most of these studies have employed rating procedures only, and have not shown the effectiveness of caffeine to reinforce behaviors other than through subjective ratings. Twenty-five participants (15 low caffeine consumers, and 10 moderate caffeine consumers) were each given three exposures to a caffeinated drink, and three exposures to a non-caffeinated drink. Each drink was associated with a particular color. At each session, they were asked to rate the pleasantness of the drink, and choose from distinctively colored sweets. The results showed an increase in the rating of pleasantness for the caffeinated drink in moderate caffeine consumers, but a decrease in rated pleasantness for low caffeine consumers. The opposite effect was seen for the non-caffeinated drink. There was an increase in consumption of the number of sweets with the same color as that of the caffeine-paired drink in the moderate caffeine consumers. These findings suggest that caffeine may serve as a negative reinforcer, and that the alleviation of withdrawal symptoms may be associated with the flavor and appearance of the caffeinated drink.  相似文献   
4.
Although, impairments following sleep deprivation have been clearly demonstrated in the literature, researchers have found a wide range of individual variation in response to sleep deprivation. The relationship between personality and the subjective and objective impact of sleep deprivation was examined using the Epworth Sleepiness Scale, Stanford Sleepiness Scale, Sleep Hygiene Index, Profile of Mood States, an oddball reaction time test, a multi-task cognitive performance battery (SynWin), and the NEO Personality Inventory Revised. Subjects (14 males, 14 females, mean age 20.5) were sleep deprived for 28–35 h and during this time were allowed access to self-reported typical amounts of tobacco, caffeine, and food. Post sleep deprivation: (a) higher neuroticism scores were related to participants feeling sleepier, experiencing more mood disturbance, and performing inferiorly on a behavioral task; (b) subjects scoring as introverts showed more compromised behavioral performance compared to extraverts. The authors suggest that potential moderating variables of the relationship between personality and sleep deprivation such as stimulant use, food intake, and socialization warrant further investigation.  相似文献   
5.
The purpose of the present study was to examine the influences of gender differences and masculinity–femininity on taste thresholds and food preferences. The participants were 108 Japanese undergraduate students (44 men and 64 women); their mean age was 19.6 years (SD = 1.3). Their detection and recognition thresholds for caffeine and sucrose were measured. Multiple regression analyses showed that women tended to have a lower detection threshold for caffeine than men did. The recognition threshold for caffeine was positively associated with scores for masculinity. For men, masculinity may be associated with smoking and drinking behavior, thereby resulting in a lower sensitivity for bitterness. Masculinity and femininity related to food preferences are also discussed.  相似文献   
6.
The effects of a 3mg/kg body weight (BW) dose of caffeine were assessed on behavioral indices of response inhibition. To meet these aims, we selected a modified AX version of the Continuous Performance Test (CPT), the stop task, and the flanker task. In three double-blind, placebo-controlled, within-subjects experiments, these tasks were administered to healthy participants. While the results for the AX-CPT were indicative of improved response inhibition after caffeine, they might also reflect caffeine-induced changes in mechanisms other than response inhibition (e.g., attentional processes). The results for the stop task and flanker task were more straightforward. That is, the effects of caffeine on overall flanker performance and selective response suppression as revealed by distribution-analytical techniques were negligible. In the stop task a global effect of caffeine on processing speed was seen, rather than specific effects on response inhibition. Taken together, these experiments showed that both active and reactive inhibition were not significantly modulated by caffeine. The present results are linked to neural circuits that underlie inhibitory control and the role of caffeine-induced strategic changes.  相似文献   
7.
Caffeine is the most widely consumed psychotropic drug in the world, with numerous studies documenting the effects of caffeine on people’s alertness, vigilance, mood, concentration, and attentional focus. The effects of caffeine on creative thinking, however, remain unknown. In a randomized placebo-controlled between-subject double-blind design the present study investigated the effect of moderate caffeine consumption on creative problem solving (i.e., convergent thinking) and creative idea generation (i.e., divergent thinking). We found that participants who consumed 200 mg of caffeine (approximately one 12 oz cup of coffee, n = 44), compared to those in the placebo condition (n = 44), showed significantly enhanced problem-solving abilities. Caffeine had no significant effects on creative generation or on working memory. The effects remained after controlling for participants’ caffeine expectancies, whether they believed they consumed caffeine or a placebo, and changes in mood. Possible mechanisms and future directions are discussed.  相似文献   
8.
Caffeinated products are often consumed as a popular countermeasure to the effects of sleep loss. However, the efficacy of caffeine to exert these effects after consecutive nights of sleep loss is poorly understood. The aim of this study was to investigate the effects of three consecutive nights of restricted sleep and morning caffeine consumption on subjective ratings of sleepiness/alertness, reaction time, and simulated driving performance. Twenty healthy, habitual caffeine consumers (11 females; age: 23.3 ± 5.7 y; BMI: 22.3 ± 3.5 kg⋅m−2; caffeine intake: 204 ± 89 mg⋅day−1; Mean ± SD) who had normal sleeping patterns (≥8 h⋅night−1) participated in this double-blind, placebo-controlled, randomised study. Following one night of normal sleep (≥8 h time in bed (TIB)), participants underwent three consecutive nights of restricted sleep (5 h TIB). Participants received caffeine (200 mg; n = 10) or placebo (n = 10) capsules each morning and all participants received caffeine (100 mg) capsules each afternoon. Subjective ratings of alertness, concentration and tiredness were measured before and 1 h after morning capsule administration. Choice Reaction Time (CRT) was examined 1 h after morning capsule administration, with response speed and accuracy as outcome variables. Driving performance was assessed using a 30 min simulated driving task, with lateral (standard deviation of lane position [SDLP]; total number of line crossings [LC]) and longitudinal (standard deviation of speed [SDSP]) measures of vehicle control as outcome variables. Alertness and concentration significantly decreased, and tiredness increased across the three days of sleep loss. Caffeine only marginally alleviated these effects. No differences were observed between treatments or across trial days for response speed and accuracy on the CRT task. Likewise, no significant differences were observed between groups or across trial days for any measures of simulated driving performance. Overall, results from this study indicate that three consecutive days of sleep loss influence subjective ratings of alertness, concentration and tiredness, but does not alter CRT or simulated driving performance. Caffeine may alleviate some of the negative subjective effects imposed by restricted sleep, but the efficacy of caffeine to attenuate performance changes in CRT and driving performance were unable to be observed.  相似文献   
9.
AimThe study examined the moderating effect of repeat-dose, chewing gum-administered caffeine on the well-established relationship between drowsiness and driving performance, under the conditions of accumulating sleep loss.Method50-h sleep deprivation protocol with a double-blind, placebo-controlled design. Eleven volunteers (6 male), aged 18–28 years were screened for pre-existing medical conditions (including sleep disturbances), tobacco and recreational drug use, recent time-zone travel and shift-work. They were randomly allocated to placebo or caffeine group and administered 4 oral doses of either caffeinated gum pellets (200 mg/dose) or non-caffeinated placebo gum every two hours (01:00, 03:00, 05:00, 07:00) on the first and second nights of the protocol. Participants were constantly monitored and remained awake for 50 h, while performing 15 identical, evenly-spaced 40-min monotonous driving tasks in a medium-fidelity moving-base driving simulator. Their drowsiness was monitored with a spectacle frame-mounted infra-red sensor registering ocular parameters and converting them into a Johns Drowsiness Scale (JDS) score every 60 s. Lane keeping and speed variability measures were used to assess driving performance.ResultsDriving performance declined and drowsiness increased from the first simulated drive to the last. When driving performance was examined in one-minute epochs synchronised with JDS scores, both lateral lane positioning and speed variability were found to be associated with drowsiness. The strength of this association was significantly weaker in the caffeine group, compared to placebo. Placebo group replicated the linear relationship between drowsiness and driving errors across the full range of JDS scores. This pattern was significantly weaker under the caffeine condition, and was even reversed at the upper range of JDS, with higher JDS scores not resulting in further degradation of driving performance. This dissociation between drowsiness and driving errors persisted across the 24-h cycle under the caffeine condition, despite caffeine being administered only during early morning hours.ConclusionStrategically timed, repeat 200 mg doses of caffeine administered via chewing gum can mitigate fatigue-induced impairments in driving performance by not only reducing drowsiness but also by significantly weakening its impact on driving errors. This dual effect of sustained drowsiness reduction and the dissociation between drowsiness levels and driving errors seems worth further investigation as it might offer an effective emergency countermeasure against driver drowsiness and its subsequent conversion into potentially fatal driving errors.  相似文献   
10.
Biological rhythms play a prominent role in the modulation of human physiology and behavior. [Smith, K., Valentino, D., & Arruda, J. (2003). Rhythmic oscillations in the performance of a sustained attention task. Journal of Clinical and Experimental Neuropsychology, 25, 561-570] suggested that sustained human performance may systematically fluctuate in a cyclic manner with periods of 1.5 min and 5.2 min. The current series of investigations sought to manipulate those periodicities by altering task difficulty, administering caffeine, and testing on a more ecologically valid task. Strong evidence of a 1.5 min periodicity was found across studies. Most participants did not demonstrate the 5.2 min periodicity. Moreover, the 1.5 min periodicity was resistant to task manipulations and appeared in similar levels across conditions in all three experiments. These rhythms may be indicative of an endogenous system that modulates sustained attention in humans. Evidence supporting this idea and implications of the research are discussed.  相似文献   
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