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臭氧共同暴露对吸入铬致癌潜力的影响。1. 对滞留以及细胞外和细胞内分布的影响。

Impact of coexposure to ozone on the carcinogenic potential of inhaled chromium. 1. effects on retention and on extra- and intracellular distribution.

作者信息

Cohen Mitchell D, Sisco Maureen, Baker Kathy, Bowser Darlene, Chen Lung-Chi, Schlesinger Richard B

机构信息

Department of Environmental Medicine, New York University School of Medicine, 57 Old Forge Road, Tuxedo, NY 10987, USA.

出版信息

J Toxicol Environ Health A. 2003 Jan 10;66(1):39-55. doi: 10.1080/15287390306459.

Abstract

A health hazard to welders is development of lung cancer. It is believed that this is likely due, in part, to the presence in welding fumes of several hexavalent chromium (Cr[VI]) species, whose solubility depends primarily on which process (i.e., manual metal arc verus metal-inert gas) is used. However, inhalation of Cr alone is uncommon in this setting. Thus, an examination of potential contributions from other coinhalants in creating or enhancing conditions whereby inhaled fume-associated Cr (primarily the insoluble forms) may initiate cancer is critical to increasing our understanding and preventing this particular occupational disease. One major chemical species formed and released during welding is ozone (O3). Though implications of adverse pulmonary effects from individual exposure to Cr or O3 have been investigated, those from simultaneous exposure are unclear. To begin to address whether the carcinogenic potential of insoluble Cr[VI] agents might be enhanced in hosts inhaling mixtures of Cr and O3 versus Cr alone, analyses of total lung Cr burden, Cr retention in lung epithelium and interstitium, and potential shifts in lung cell distribution of Cr from the cytoplasm to nuclei were undertaken in F-344 rats exposed nose-only (5 h/d, 5 d/wk for up to 48 wk) to an extrapolated occupationally relevant level of Cr (360 micrograms Cr/m3 as calcium chromate) alone and in combination with 0.3 ppm O3. Overall, there was only a nominal effect from O3 on Cr retention or on distribution of Cr particles among extracellular sites and within lung cells. However, there were O3-related effects upon mechanisms for clearing the Cr from the deep lung, specifically at the levels of particle uptake and postphagocytic/endocytic processing by macrophages. This O3 exposure-related shift in normal pulmonary clearance might potentially increase the health risk in workers exposed to other insoluble or poorly soluble carcinogenic Cr compounds.

摘要

对焊工来说,一种健康危害是肺癌的发生。据信,这可能部分归因于焊接烟尘中存在几种六价铬(Cr[VI])物质,其溶解度主要取决于所使用的工艺(即手工金属电弧焊与熔化极惰性气体保护焊)。然而,在这种情况下,单独吸入铬并不常见。因此,研究其他共吸入物在创造或增强条件方面的潜在作用,使吸入烟尘相关的铬(主要是不溶性形式)引发癌症,对于增进我们的理解和预防这种特定的职业病至关重要。焊接过程中形成并释放的一种主要化学物质是臭氧(O3)。虽然已经研究了个体接触铬或臭氧对肺部产生不良影响的情况,但同时接触两者的影响尚不清楚。为了开始探讨在吸入铬和臭氧混合物的宿主中,不溶性Cr[VI]物质的致癌潜力是否会比单独吸入铬时增强,对仅经鼻暴露(每天5小时,每周5天,长达48周)于外推至职业相关水平的铬(以铬酸钙计为360微克铬/立方米)单独以及与0.3 ppm臭氧组合的F-344大鼠进行了全肺铬负荷、肺上皮和间质中铬保留以及铬在肺细胞中从细胞质到细胞核的潜在分布变化分析。总体而言,臭氧对铬保留或铬颗粒在细胞外部位和肺细胞内的分布仅有轻微影响。然而,臭氧对从深部肺清除铬的机制有相关影响,特别是在巨噬细胞摄取颗粒和吞噬后/内吞处理的水平上。这种与臭氧暴露相关的正常肺清除变化可能会增加接触其他不溶性或难溶性致癌铬化合物的工人的健康风险。

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