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大鼠中丙二醇二硝酸酯对运动表现的影响

Motor performance effects of propylene glycol dinitrate in the rat.

作者信息

Bogo V, Hill T A, Nold J

出版信息

J Toxicol Environ Health. 1987;22(1):17-27. doi: 10.1080/15287398709531047.

Abstract

Propylene glycol dinitrate (PGDN), a major constituent of a liquid torpedo propellant, produces incoordination and impairment of balance in humans. This study was conducted to evaluate the rat as a model for PGDN-induced motor performance decrement, and to determine if direct application of PGDN onto neural tissue is a useful alternative to other routes of exposure. PGDN was injected onto the cisterna magna (ic) of adult Sprague-Dawley rats trained on the accelerod, a test of motor performance. Three groups of 13-14 male rats each received a single dose of either 5 or 10 microliters PGDN or 25 microliters sterile saline (control) while anesthetized with halothane. Accelerod performance was measured 12 min after ic injection, then hourly for 6 h, and at 24 h. Injections were evaluated using a five-stage screening criterion to eliminate grossly traumatized subjects, to verify the accuracy of the injection, and to determine the extent of mechanical damage. Eighteen out of 41 subjects passed the five-stage screen. A significant decrease in performance occurred during the first 2 h following injection of 10 microliters PGDN compared to the control and the 5-microliters groups. N significant differences were seen between the 5-microliter and control groups. These data confirm previous findings of PGDN-induced changes in human motor performance, suggesting that the rat may be a useful model for further PGDN neurobehavioral assessment. The data also indicate that ic injection may be an effective alternative to other routes of exposure for materials with appropriate chemical and biological properties if an evaluation screen is used.

摘要

丙二醇二硝酸酯(PGDN)是液体鱼雷推进剂的主要成分,可导致人体出现共济失调和平衡受损。本研究旨在评估大鼠作为PGDN诱导运动性能下降模型的可行性,并确定将PGDN直接应用于神经组织是否是比其他暴露途径更有效的方法。将PGDN注射到在加速度计上训练的成年Sprague-Dawley大鼠的大池(ic)中,加速度计是一种运动性能测试。三组,每组13 - 14只雄性大鼠,在使用氟烷麻醉时,分别接受5或10微升PGDN或25微升无菌盐水(对照)的单次剂量注射。在ic注射后12分钟测量加速度计性能,然后每小时测量6小时,并在24小时测量。使用五阶段筛选标准对注射进行评估,以排除严重受伤的受试者,验证注射的准确性,并确定机械损伤的程度。41只受试者中有18只通过了五阶段筛选。与对照组和5微升组相比,注射10微升PGDN后的前2小时内性能显著下降。5微升组和对照组之间未观察到显著差异。这些数据证实了之前关于PGDN引起人体运动性能变化的研究结果,表明大鼠可能是进一步进行PGDN神经行为评估的有用模型。数据还表明,如果使用评估筛选,对于具有适当化学和生物学特性的物质,ic注射可能是替代其他暴露途径的有效方法。

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