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吸入氡后呼吸道中微核的诱导。

Induction of micronuclei in respiratory tract following radon inhalation.

作者信息

Brooks A L, Bao S, Harwood P W, Wood B H, Chrisler W B, Khan M A, Gies R A, Cross F T

机构信息

Washington State University at Tricities, Richland 99352, USA.

出版信息

Int J Radiat Biol. 1997 Nov;72(5):485-95. doi: 10.1080/095530097142988.

Abstract

Male Wistar rats were exposed to radon and its progeny (0.0, 60, 262 and 564 working level months, WLM), and the frequency of micronuclei was determined in deep lung fibroblasts, and deep lung, trachea and nasal epithelial cells with slopes of 0.28, 0.67, 0.34 and 0.11 micronuclei/1000 binucleated cells/WLM respectively. Micronuclei in deep lung fibroblasts, isolated and cultured using two methods and media, demonstrated no differences in slopes. Biological damage was used as a biodosimeter to calculate the relationship between dosimetric units: alpha particle traversals or 'nuclear hits', dose in mGy and exposure in WLM. The estimated number of nuclear alpha traversals/Gy was 6.3. Radon exposure to 170 WLM resulted in the same frequency of micronuclei in deep lung epithelial cells as produced by one alpha hit/cell nucleus. Absorbed dose/unit of exposure (mGy/WLM) was estimated assuming the damage was related to absorbed dose or to changes in cell sensitivity and ranged from 1.13 to 1.34 for deep lung epithelial cells, 0.47 to 1.09 for deep lung fibroblasts, 0.34 to 0.67 for tracheal epithelial cells and 0.18 to 0.33 for nasal epithelial cells. Biological dosimetry can be used to relate exposure to damage, compare dosimetric units and validate physical dosimetry models. This approach can be applied to any inhaled material capable of producing biological damage.

摘要

将雄性Wistar大鼠暴露于氡及其子体(0.0、60、262和564工作水平月,WLM),并测定深肺成纤维细胞以及深肺、气管和鼻上皮细胞中的微核频率,其斜率分别为0.28、0.67、0.34和0.11微核/1000个双核细胞/WLM。使用两种方法和培养基分离培养的深肺成纤维细胞中的微核,其斜率无差异。生物损伤被用作生物剂量计,以计算剂量学单位之间的关系:α粒子穿越或“核撞击”、毫戈瑞(mGy)剂量和WLM暴露量。估计每戈瑞的核α穿越数为6.3。暴露于170 WLM的氡导致深肺上皮细胞中的微核频率与每个细胞核一次α撞击所产生的频率相同。假设损伤与吸收剂量或细胞敏感性变化有关,估计了每单位暴露的吸收剂量(mGy/WLM),深肺上皮细胞的范围为1.13至1.34,深肺成纤维细胞为0.47至1.09,气管上皮细胞为0.34至0.67,鼻上皮细胞为0.18至0.33。生物剂量测定可用于将暴露与损伤联系起来,可以比较剂量学单位并验证物理剂量学模型。这种方法可应用于任何能够产生生物损伤的吸入物质。

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