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吸入木烟后绵羊肺部氧化应激的评估。

Assessment of oxidative stress in lungs from sheep after inhalation of wood smoke.

作者信息

Park Myung S, Cancio Leopoldo C, Jordan Bryan S, Brinkley William W, Rivera Victor R, Dubick Michael A

机构信息

US Army Institute of Surgical Research, Fort Sam Houston, TX 78234-6315, USA.

出版信息

Toxicology. 2004 Feb 15;195(2-3):97-112. doi: 10.1016/j.tox.2003.09.005.

Abstract

To elucidate potential dose-dependent mechanisms associated with wood smoke inhalation injury, the present study evaluated antioxidant status and the extent of pulmonary injury in sheep after graded exposure to smoke. Adult, male sheep (n=4-5 per group) were anesthetized and received 0, 5, 10 or 16 units of cooled western pine bark smoke, corresponding to 0, 175, 350 and 560 s, respectively, of smoke dwell time in the airways and lung. Smoke was mixed at a 1:1 ratio with 100% O2 to minimize hypoxia. Plasma and expired breath samples were collected pre-smoke, and 6, 12, 18, 24, 36 and 48 h after smoke exposure. Sheep were euthanatized 48 h after smoke exposure and lung and airway sections were evaluated histologically for injury and biochemically for indices of oxidative stress. Plasma thiobarbituric acid reactive substances (TBARS) were 66 and 69% higher than controls after moderate and severe smoke exposure at 48 h, whereas total antioxidant potential was not statistically different among groups at any time after exposure. Lung TBARS showed a dose-dependent response to smoke inhalation and were approximately 2-, 3- and 4-fold higher, respectively, than controls after exposure to 5, 10 and 16 units of smoke. Lung myeloperoxidase (MPO) activity was also higher in smoke-exposed animals than controls, and MPO activity was markedly elevated (19- and 22-fold higher than controls in right apical and medial lobes) in response to severe smoke exposure. Smoke exposure also induced a dose-dependent injury to tracheobronchial epithelium and lung parenchyma. Taken together these data show that few indices of oxidative stress responded in a dose-dependent manner to graded doses of smoke inhalation, although most of the indices measured in lung were affected by the highest dose of smoke. Additional time course studies are necessary to determine whether these oxidants are a cause or a consequence of the airway and lung injury associated with exposure to wood smoke.

摘要

为阐明与吸入木烟损伤相关的潜在剂量依赖性机制,本研究评估了绵羊在分级暴露于烟雾后抗氧化状态及肺损伤程度。成年雄性绵羊(每组4 - 5只)麻醉后,分别吸入0、5、10或16单位冷却的西部松树皮烟雾,对应气道和肺中烟雾停留时间分别为0、175、350和560秒。烟雾与100%氧气按1:1比例混合以尽量减少缺氧。在烟雾暴露前、暴露后6、12、18、24、36和48小时采集血浆和呼出气体样本。烟雾暴露48小时后对绵羊实施安乐死,对肺和气道切片进行组织学损伤评估及氧化应激指标的生化评估。48小时时,中度和重度烟雾暴露后血浆硫代巴比妥酸反应性物质(TBARS)比对照组分别高66%和69%,而暴露后任何时间各组总抗氧化能力无统计学差异。肺TBARS对吸入烟雾呈剂量依赖性反应,暴露于5、10和16单位烟雾后分别比对照组高约2倍、3倍和4倍。烟雾暴露动物肺髓过氧化物酶(MPO)活性也高于对照组,重度烟雾暴露时MPO活性显著升高(右上叶和中叶比对照组高19倍和22倍)。烟雾暴露还导致气管支气管上皮和肺实质出现剂量依赖性损伤。综合这些数据表明,尽管肺中测量的大多数指标受最高剂量烟雾影响,但很少有氧化应激指标对分级剂量的吸入烟雾呈剂量依赖性反应。需要进一步的时间进程研究来确定这些氧化剂是与木烟暴露相关的气道和肺损伤的原因还是结果。

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