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首页> 外文期刊>Pulmonary pharmacology & therapeutics >Humic acid enhances cigarette smoke-induced lung emphysema in mice and IL-8 release of human monocytes.
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Humic acid enhances cigarette smoke-induced lung emphysema in mice and IL-8 release of human monocytes.

机译:腐殖酸增强了香烟引起的小鼠肺气肿,并增强了人类单核细胞的IL-8释放。

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摘要

Tobacco smoke is the main factor in the etiology of lung emphysema. Generally prolonged, substantial exposure is required to develop the disease. Humic acid is a major component of cigarette smoke that accumulates in smokers' lungs over time and induces tissue damage. OBJECTIVES: To investigate whether humic acid pre-loading potentiates the development of cigarette smoke-induced lung emphysema in mice and increases IL-8 release by human monocytes. METHODS: C57BL/6J mice received humic acid or aqueous vehicle by tracheal installation on day 0 and day 7. From day 21 to day 84, the mice were exposed to cigarette smoke or clean air for 5 days/week. Twenty-four hours after the last exposure we determined leukocytes in lung lavage, heart hypertrophy and alveolar wall destruction. Human monocytes were incubated with cigarette smoke extract (CSE), humic acid or the combination overnight. RESULTS: Humic acid nor cigarette smoke caused alveolar wall destruction within two months. Interestingly, the combination did induce lung emphysema. Humic acid, cigarette smoke or the combination did not change leukocyte types and numbers in lung lavage fluid, but the combination caused peribronchiolar and perivascular lymphocyte infiltration. Humic acid treatment resulted in a high proportion of alveolar macrophages heavily loaded with intracellular granula. Humic acid also induces the release of IL-8 from human monocytes and enhances the CSE-induced IL-8 release. CONCLUSIONS: Humic acid deposition in the lungs potentiates the development of cigarette smoke-induced interstitial inflammation and lung emphysema. Moreover, humic acid promotes IL-8 release from human monocytes. Since humic acid accumulates steadily in the lungs of smokers, this may provide an explanation for the natural history on late onset of this disease. The model described here offers a novel way to study emphysema and may direct the search for new therapeutic approaches.
机译:烟草烟雾是肺气肿病因的主要因素。通常延长时间,需要大量接触才能发展该病。腐殖酸是香烟烟雾的主要成分,随着时间的推移,它会积聚在吸烟者的肺中并引起组织损伤。目的:研究腐殖酸预加载是否能增强小鼠香烟烟雾诱发的肺气肿的发生并增加人类单核细胞的IL-8释放。方法:C57BL / 6J小鼠在第0天和第7天通过气管安装接受腐殖酸或水性赋形剂。从第21天到第84天,将小鼠暴露于香烟烟雾或清洁空气中,持续5天/周。在最后一次暴露后二十四小时,我们确定了肺灌洗,心脏肥大和肺泡壁破坏中的白细胞。将人单核细胞与香烟烟雾提取物(CSE),腐殖酸或上述混合物孵育过夜。结果:腐殖酸或香烟烟雾在两个月内引起肺泡壁破坏。有趣的是,该组合确实诱发了肺气肿。腐殖酸,香烟烟雾或二者的结合并没有改变肺灌洗液中的白细胞类型和数量,但是这些结合导致细支气管周和血管周淋巴细胞浸润。腐殖酸处理导致大量细胞内颗粒重载的肺泡巨噬细胞。腐殖酸还诱导人单核细胞释放IL-8,并增强CSE诱导的IL-8释放。结论:肺中的腐殖酸沉积增强了香烟烟雾引起的间质性炎症和肺气肿的发生。此外,腐殖酸促进人单核细胞释放IL-8。由于腐殖酸在吸烟者的肺中稳定积累,因此可以解释这种疾病迟发的自然病史。这里描述的模型提供了一种研究肺气肿的新颖方法,并且可以指导寻找新的治疗方法。

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