Active oxygen formation in alveolar macrophage and pulmonary tumorigenesis.

T Yano, T Ichikawa
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Abstract

Glycerol enhances pulmonary tumorigenesis in mice treated with 4-nitroquinoline 1-oxide (4NQO). In order to evaluate factors that contribute to the enhancing effect of glycerol on 4NQO-induced pulmonary tumorigenesis, we selected alveolar macrophage (AM) as a source of active oxygen formation in the lung and investigated the effects of glycerol on active oxygen formation in AMs treated with 4NQO. AMs were stimulated with opsonized zymosan, and active oxygen formation in AMs was examined after stimulation. Continuous glycerol treatment within 4 weeks after 4NQO injection has no influence on the capacity of active oxygen generation in AMs (expressed as maximum count of chemiluminescence) and the total amount of active oxygen generation in AMs (expressed as total count of chemiluminescence). These results suggest that active oxygen formation in AMs does not contribute to enhance 4NQO-induced pulmonary tumorigenesis in mice treated with glycerol.

肺泡巨噬细胞活性氧形成与肺肿瘤发生。
甘油促进4-硝基喹啉1-氧化物(4NQO)处理小鼠的肺肿瘤发生。为了评估甘油对4NQO诱导的肺肿瘤发生增强作用的因素,我们选择肺泡巨噬细胞(AM)作为肺中活性氧形成的来源,并研究甘油对4NQO处理的AM活性氧形成的影响。用调理酶刺激am,观察刺激后am的活性氧形成情况。注射4NQO后4周内持续甘油处理对AMs活性氧生成能力(以最大化学发光计数表示)和AMs活性氧生成总量(以总化学发光计数表示)无影响。这些结果表明,在甘油处理的小鼠中,AMs中活性氧的形成并没有促进4nqo诱导的肺肿瘤发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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