Suppr超能文献

[氯化钡预处理对急性呼吸窘迫综合征小鼠肺组织的保护作用]

[Protective effect of barium chloride pretreatment on lung in mice with acute respiratory distress syndrome].

作者信息

Wang Yanxue, Yang Hongna, Li Wenyu, Yu Xiaoyi, Wang Chunting, Fang Wei

机构信息

Department of Critical Care Medicine, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250101, Shandong, China.

Shandong University, Jinan 250101, Shandong, China. Corresponding author: Fang Wei, Email:

出版信息

Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2023 Mar;35(3):274-277. doi: 10.3760/cma.j.cn121430-20221020-00932.

Abstract

OBJECTIVE

To explore whether barium chloride (BaCl) preconditioning has the protective effect on lipopolysaccharide (LPS)-induced acute respiratory distress syndrome (ARDS) model in mice and the possible mechanism.

METHODS

Sixty 8-12 week old healthy C57BL/6 male mice were randomly divided into control group, ARDS model group and BaCl pretreatment group, with 20 mice in each group. The BaCl pretreatment group was continuously injected with BaCl (4 mg/kg through the tail vein) for 3 days before ARDS model establishment. ARDS model was established by intratracheally injecting (3 mg/kg) LPS. The control group was intratracheally given the same volume of 0.9% normal saline. On 24th hour after ARDS model establishment, some mice were sacrificed for obtaining fresh lung tissue. And the right lower lobe of the lung was separated for observing the pathological changes of lung tissue while the left lung tissue was used to measure the wet/dry weight ratio (W/D) of the lung. Some mice were sacrificed for observing pulmonary microvascular permeability at 2nd hours after injecting Evans blue (EB) through tail vein. The left mice were killed for alveolar lavage to measure the levels of tumor necrosis factor-α (TNF-α) via enzyme linked immunosorbent assay (ELISA).

RESULTS

Comparing with the control group, ARDS model group showed typical ARDS pathological changes, which included the increased W/D ratio (4.951±0.161 vs. 3.449±0.299, P < 0.01) and the content of EB in the lung tissue (μg/g: 0.130±0.027 vs. 0.085±0.011, P < 0.01), the damaged alveolar wall structure, lung congestion and exudates in the alveoli, as well as amounts of inflammatory cells. The pathological score of lung injury (10.33±1.15 vs. 1.67±0.58) and the level of TNF-α in BALF (ng/L: 900.85±247.80 vs. 68.21±5.79) were significantly increased in the ARDS model group (both P < 0.01). Comparing with the ARDS model group, the lung W/D ratio (4.620±0.125 vs. 4.951±0.161) and the EB content in the lung tissue (μg/g: 0.108±0.011 vs. 0.130±0.027) of BaCl pretreatment group were significantly reduced (both P < 0.01). And the damaged pulmonary structural BaCl pretreatment group were significantly alleviated. In addition, the pulmonary pathological score (5.00±1.00 vs. 10.33±1.15) and the level of TNF-α in BALF (ng/L: 169.16±73.33 vs. 900.85±247.80) were significantly decreased (both P < 0.01).

CONCLUSIONS

Barium chloride pretreatment can improve the lung histopathological changes of ARDS model mice induced by LPS by reducing the permeability of pulmonary capillaries and local inflammatory reaction.Barium chloride has the protective effect against LPS attack in mice model of ARDS.

摘要

目的

探讨氯化钡(BaCl)预处理对脂多糖(LPS)诱导的小鼠急性呼吸窘迫综合征(ARDS)模型是否具有保护作用及其可能机制。

方法

将60只8-12周龄健康C57BL/6雄性小鼠随机分为对照组、ARDS模型组和BaCl预处理组,每组20只。BaCl预处理组在建立ARDS模型前连续3天经尾静脉注射BaCl(4mg/kg)。通过气管内注射(3mg/kg)LPS建立ARDS模型。对照组气管内给予相同体积的0.9%生理盐水。在建立ARDS模型后24小时,处死部分小鼠获取新鲜肺组织。分离右肺下叶观察肺组织病理变化,左肺组织用于测量肺组织湿/干重比(W/D)。在经尾静脉注射伊文思蓝(EB)后2小时处死部分小鼠观察肺微血管通透性。处死剩余小鼠进行肺泡灌洗,通过酶联免疫吸附测定(ELISA)法检测支气管肺泡灌洗液(BALF)中肿瘤坏死因子-α(TNF-α)水平。

结果

与对照组比较,ARDS模型组呈现典型的ARDS病理变化,包括W/D比值升高(4.951±0.161比3.449±0.299,P<0.01)、肺组织中EB含量增加(μg/g:0.130±0.027比0.085±0.011,P<0.01)、肺泡壁结构破坏、肺淤血及肺泡内有渗出物,还有大量炎性细胞。ARDS模型组肺损伤病理评分(10.33±1.15比1.67±0.58)及BALF中TNF-α水平(ng/L:900.85±247.80比68.21±5.79)均显著升高(均P<0.01)。与ARDS模型组比较,BaCl预处理组肺W/D比值(4.620±0.125比4.951±0.161)及肺组织中EB含量(μg/g:0.108±0.011比0.130±0.027)均显著降低(均P<0.01)。且BaCl预处理组肺结构损伤明显减轻。此外,肺病理评分(5.00±1.00比10.33±1.15)及BALF中TNF-α水平(ng/L:169.16±73.33比900.85±247.80)均显著降低(均P<0.01)。

结论

氯化钡预处理可通过降低肺毛细血管通透性及局部炎症反应改善LPS诱导的ARDS模型小鼠的肺组织病理变化。氯化钡对ARDS小鼠模型的LPS攻击具有保护作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验