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反复吸入臭氧会减轻气道损伤/修复以及P物质的释放,但不会减轻适应性。

Repeated episodes of ozone inhalation attenuates airway injury/repair and release of substance P, but not adaptation.

作者信息

Schelegle Edward S, Walby William F, Alfaro Mario F, Wong Viviana J, Putney Lei, Stovall Mary Y, Sterner-Kock Anja, Hyde Dallas M, Plopper Charles G

机构信息

Department of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine, University of California, Davis, CA 95616, USA.

出版信息

Toxicol Appl Pharmacol. 2003 Feb 1;186(3):127-42. doi: 10.1016/s0041-008x(02)00026-1.

Abstract

To determine the impact of repeated episodes of ozone exposure on physiologic adaptation, epithelial injury/repair, and tracheal substance P levels, adult rats were subjected to episodes of ozone (5 days, 1 ppm, 8 h/day) followed by 9 days of filtered air for four cycles. Rats were sampled on days 1 and 5 of each episode and 9 days after day 5 of episodes 1, 2, and 4. One hour before being euthanized each rat was injected with 5-bromo-2'-deoxyuridine to label proliferating cells. Each 5-day episode showed a characteristic pattern of rapid shallow breathing (days 1 and 2), epithelial injury, and interstitial and intraluminal inflammation. In contrast, the neutrophil component of inflammation, tracheal substance P release, and cell proliferation became attenuated with each consecutive episode of exposure. Concurrent with this cyclic and attenuated response there was progressive hypercellularity and hyperplasia in all airways studied and a progressive remodeling present in the terminal bronchioles. Our findings are consistent with the notion that the cumulative distal airway lesion is at least in part the result of a depressed cell proliferative response to injury in these airways. This depressed cell proliferative response may be in part the result of diminished neutrophil inflammation and/or release of mitogenic neuropeptides in response to ozone-induced injury.

摘要

为了确定反复暴露于臭氧对生理适应、上皮损伤/修复以及气管P物质水平的影响,成年大鼠经历了臭氧暴露阶段(5天,1 ppm,每天8小时),随后是9天的过滤空气,共四个循环。在每个暴露阶段的第1天和第5天以及第1、2和4阶段第5天后的第9天对大鼠进行采样。在处死每只大鼠前1小时,注射5-溴-2'-脱氧尿苷以标记增殖细胞。每个5天的暴露阶段都呈现出快速浅呼吸(第1天和第2天)、上皮损伤以及间质和管腔内炎症的特征性模式。相比之下,随着连续暴露阶段的增加,炎症的中性粒细胞成分、气管P物质释放和细胞增殖均减弱。伴随着这种周期性和减弱的反应,在所研究的所有气道中均出现了进行性细胞增多和增生,并且在终末细支气管中存在进行性重塑。我们的研究结果与以下观点一致,即累积的远端气道病变至少部分是这些气道中对损伤的细胞增殖反应受到抑制的结果。这种细胞增殖反应受到抑制可能部分是由于中性粒细胞炎症减轻和/或对臭氧诱导损伤的促有丝分裂神经肽释放减少所致。

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