Newland M C
Department of Psychology, Auburn University, AL 36849, USA.
Neurotoxicology. 1999 Apr-Jun;20(2-3):415-32.
Manganese's neurotoxicity continues to present a puzzling array of differences across individuals and across published reports in the profile of effects seen in humans and nonhuman species, but some of the sources of individual variability are becoming clear from studies of animals. The kinetics of manganese is a critical component of any assessment of risk associated with exposure. After inhalation, the uptake of manganese into and elimination from the central nervous system are slow and some manganese remains in the nervous system a year after inhalation. Comparison with other parenteral routes suggests that manganese depots in lung prolongs exposure even after environmental exposure has ended. Manganese's neurotoxicity is associated with its appearance in basal ganglia structures, especially the globus pallidus. Manganese also appears in the pituitary gland but the functional consequences of this are not well understood. Other critical components in characterizing manganese's neurotoxicity appear to be the behavioral endpoints used, the species studied, and the exposure rate. Over neurological signs and excitability are associated with high exposure rates and the appearance of manganese throughout basal ganglia and basal forebrain regions. More focused behavioral endpoints are required to detect the subtle signs associated with slow exposure rates low exposure levels, but when such designs are used the effect is unequivocal. At lower exposure levels, doses of 5 mg/kg and greater, deficits in a task in which a monkey executed a rowing type motion against a spring approximating its body weight were clearly related to manganese exposure while other traditional measures of response patterns under schedules of reinforcement remained intact. Excitability and other signs of emotionality have not been reported at low exposure rates. In rodents, manganese accumulation and alterations in the function or concentration of neurotransmitters have been reported. Investigations of behavioral effects in these species, which usually involved locomotor activity, have resulted in less consistent results. Manganese produces a constellation of neurotoxic signs whose appearance and detection are influenced by dose and exposure rate. Despite investigations of manganese's neurotoxicity in animals over a wide range of exposure levels, a NOAEL has not been identified.
锰的神经毒性在个体之间以及已发表的关于人类和非人类物种影响的报告中,仍然呈现出一系列令人困惑的差异,但从动物研究中,一些个体差异的来源正逐渐清晰。锰的动力学是任何与暴露相关风险评估的关键组成部分。吸入后,锰进入中枢神经系统并从中消除的过程缓慢,吸入一年后仍有一些锰残留在神经系统中。与其他非肠道途径相比,表明肺部的锰储存库即使在环境暴露结束后仍会延长暴露时间。锰的神经毒性与其在基底神经节结构,尤其是苍白球中的出现有关。锰也出现在垂体中,但其功能后果尚未得到很好的理解。表征锰神经毒性的其他关键因素似乎是所使用的行为终点、所研究的物种以及暴露率。过度的神经体征和兴奋性与高暴露率以及锰在整个基底神经节和基底前脑区域的出现有关。需要更有针对性的行为终点来检测与低暴露率和低暴露水平相关的细微体征,但当采用此类设计时,效果是明确的。在较低暴露水平下,剂量为5毫克/千克及以上时,猴子在执行一项对抗近似其体重的弹簧进行划船式运动任务中的缺陷与锰暴露明显相关,而在强化时间表下其他传统的反应模式测量指标保持不变。低暴露率时未报告兴奋性和其他情绪性体征。在啮齿动物中,已报告了锰的积累以及神经递质功能或浓度的改变。对这些物种行为影响的研究,通常涉及运动活动,结果不太一致。锰会产生一系列神经毒性体征,其出现和检测受剂量和暴露率的影响。尽管在广泛的暴露水平范围内对动物进行了锰神经毒性的研究,但尚未确定无观察到有害作用水平。