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短期暴露于老化且稀释的侧流香烟烟雾会加重臭氧诱导的B6C3F1小鼠肺损伤。

Short-term exposure to aged and diluted sidestream cigarette smoke enhances ozone-induced lung injury in B6C3F1 mice.

作者信息

Yu Mang, Pinkerton Kent E, Witschi Hanspeter

机构信息

Center for Comparative Respiratory Biology and Medicine, Institute of Toxicology and Environmental Health, and California Regional Primate Research Center, University of California, One Shields Avenue, Davis, California 95616, USA.

出版信息

Toxicol Sci. 2002 Jan;65(1):99-106. doi: 10.1093/toxsci/65.1.99.

Abstract

To determine the effects of aged and diluted sidestream cigarette smoke (ADSS) as a surrogate of environmental tobacco smoke (ETS) on ozone-induced lung injury, male B6C3F1 mice were exposed to (1) filtered air (FA), (2) ADSS, (3) ozone, or (4) ADSS followed by ozone (ADSS/ozone). Exposure to ADSS at 30 mg/m3 of total suspended particulates (TSP) for 6 h/day for 3 days, followed by exposure to ozone at 0.5 ppm for 24 h was associated with a significant increase in the number of cells recovered by bronchoalveolar lavage (BAL) compared with exposure to ADSS alone or ozone alone. The proportion of neutrophils and lymphocytes, as well as total protein level in BAL, was also significantly elevated following ADSS/ozone exposure, when compared with all other groups. Within the centriacinar regions of the lungs, the percentage of proliferating cells identified by bromodeoxyuridine (BrdU) labeling was unchanged from control, following exposure to ADSS alone, but was significantly elevated following exposure to ozone (280% of control) and further augmented in a statistically significant manner in mice exposed to ADSS/ozone (402% of control). Following exposure to ozone or ADSS/ozone, the ability of alveolar macrophages (AM) to release interleukin (IL)-6 under lipopolysaccharide (LPS) stimulation was significantly decreased, while exposure to ADSS or ADSS/ozone caused a significantly increased release of tumor necrosis factor alpha from AM under LPS stimulation. We conclude that ADSS exposure enhances the sensitivity of animals to ozone-induced lung injury.

摘要

为了确定作为环境烟草烟雾(ETS)替代物的老化稀释侧流香烟烟雾(ADSS)对臭氧诱导的肺损伤的影响,将雄性B6C3F1小鼠暴露于(1)过滤空气(FA)、(2)ADSS、(3)臭氧或(4)ADSS后再暴露于臭氧(ADSS/臭氧)环境中。以30毫克/立方米的总悬浮颗粒物(TSP)浓度,每天暴露于ADSS 6小时,持续3天,随后以0.5 ppm的浓度暴露于臭氧24小时,与单独暴露于ADSS或单独暴露于臭氧相比,支气管肺泡灌洗(BAL)回收的细胞数量显著增加。与所有其他组相比,ADSS/臭氧暴露后,BAL中的中性粒细胞和淋巴细胞比例以及总蛋白水平也显著升高。在肺的终末细支气管周围区域,单独暴露于ADSS后,用溴脱氧尿苷(BrdU)标记鉴定的增殖细胞百分比与对照组相比没有变化,但暴露于臭氧后显著升高(为对照组的280%),并且在暴露于ADSS/臭氧的小鼠中以统计学显著方式进一步增加(为对照组的402%)。暴露于臭氧或ADSS/臭氧后,肺泡巨噬细胞(AM)在脂多糖(LPS)刺激下释放白细胞介素(IL)-6的能力显著降低,而暴露于ADSS或ADSS/臭氧会导致AM在LPS刺激下肿瘤坏死因子α的释放显著增加。我们得出结论,暴露于ADSS会增强动物对臭氧诱导的肺损伤的敏感性。

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