Dick R B, Krieg E F, Setzer J, Taylor B
Department of Health and Human Services, Centers for Disease Control, National Institute for Occupational Safety and Health, Cincinnati, Ohio 45226.
Fundam Appl Toxicol. 1992 Oct;19(3):453-73. doi: 10.1016/0272-0590(92)90185-k.
Subjects were tested for neurobehavioral performance in an environmental chamber to detect the presence of subclinical central nervous system effects from 4-hr exposures to methyl isobutyl ketone (MIBK) at 100 ppm, methyl ethyl ketone (MEK) at 200 ppm, MIBK at 50 ppm with MEK at 100 ppm, or a placebo (i.e., a 5-min presentation of 25 ppm MEK-MIBK at each exposure period outset). Subjects were 68 males and 75 females recruited from local universities; ages ranged from 18 to 32 years. Ethanol by ingestion (95%-0.84 ml/kg) was used as a positive control. Five psychomotor tests (choice reaction time [CRT], simple reaction time [SRT], visual vigilance, dual task [auditory tone discrimination and tracking], memory scanning), one sensorimotor test (postural sway), and a test of mood (profile of mood states) were used to measure neurobehavioral effects. Additionally, chemical measurements (blood and breath) and reports of sensory and irritant effects were measured. The chemical exposures produced statistically significant performance effects on only 4 of 32 measures (% correct responses-visual vigilance, movement time-CRT, SRT, % incorrect responses-dual task). These effects, however, were not substantial and could not be attributed directly to the chemical exposures. Alcohol ingestion, however, produced significant decrements on every performance test except memory scanning and mood. An interaction occurred between gender and alcohol ingestion, such that more statistically significant performance decrements were found for females than for males. Significant odor sensations and irritant effects were reported by the subjects during the chemical exposures. The MEK results agree with earlier MEK experiments at comparable exposure conditions, and the MIBK results are consistent with a recent Swedish study that used MIBK exposures and showed no significant behavioral performance decrements from single MIBK exposures at 50 ppm with 50 W exercise. Additionally, the MIBK-MEK combination exposure showed no evidence of any interaction effects on either the behavioral or chemical measurements. The principal effects resulting from exposures to MEK and MIBK at the durations and concentrations used in the study are limited to sensory and irritant effects.
在环境舱中对受试者进行神经行为表现测试,以检测 4 小时暴露于 100 ppm 的甲基异丁基酮(MIBK)、200 ppm 的甲基乙基酮(MEK)、50 ppm 的 MIBK 与 100 ppm 的 MEK 或安慰剂(即在每个暴露期开始时呈现 5 分钟的 25 ppm MEK - MIBK)后是否存在亚临床中枢神经系统效应。受试者为从当地大学招募的 68 名男性和 75 名女性;年龄在 18 至 32 岁之间。通过摄入乙醇(95% - 0.84 ml/kg)作为阳性对照。使用五项心理运动测试(选择反应时间[CRT]、简单反应时间[SRT]、视觉警觉、双重任务[听觉音调辨别和追踪]、记忆扫描)、一项感觉运动测试(姿势摇摆)和一项情绪测试(情绪状态剖面图)来测量神经行为效应。此外,还进行了化学测量(血液和呼气)以及感觉和刺激效应报告。化学暴露仅对 32 项测量中的 4 项产生了统计学上显著的表现效应(视觉警觉的正确反应百分比、CRT 的运动时间、SRT、双重任务的错误反应百分比)。然而,这些效应并不显著,不能直接归因于化学暴露。然而,摄入酒精除了对记忆扫描和情绪外,在每项表现测试中都产生了显著的下降。性别与酒精摄入之间存在相互作用,女性在统计学上的表现下降比男性更显著。受试者在化学暴露期间报告了明显的气味感觉和刺激效应。MEK 的结果与早期在类似暴露条件下的 MEK 实验一致,MIBK 的结果与瑞典最近一项使用 MIBK 暴露的研究一致,该研究表明在 50 ppm 且有 50 瓦运动的情况下,单次 MIBK 暴露不会导致显著的行为表现下降。此外,MIBK - MEK 联合暴露在行为或化学测量方面均未显示出任何相互作用效应的证据。在本研究中使用的持续时间和浓度下,暴露于 MEK 和 MIBK 产生的主要影响仅限于感觉和刺激效应。