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熊去氧胆酸可预防脂肪栓塞综合征所致的肺损伤。

Ursodeoxycholic acid protects against lung injury induced by fat embolism syndrome.

作者信息

Niu Fangfang, Li Huafei, Xu Xiaotao, Sun Lingling, Gan Ning, Wang Aizhong

机构信息

Department of Anesthesiology, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China.

Precision Medicine Center, Taizhou Central Hospital (Taizhou University Hospital), Taizhou, China.

出版信息

J Cell Mol Med. 2020 Dec;24(24):14626-14632. doi: 10.1111/jcmm.15985. Epub 2020 Nov 4.

Abstract

Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) is a life-threatening disease with a high mortality rate, which was a common complication of fat embolism syndrome (FES). Ursodeoxycholic acid (UDCA) has been reported to exert potent anti-inflammatory effects under various conditions. In vivo, perinephric fat was injected via tail vein to establish a rat FES model, the anti-inflammatory effects of UDCA on FES-induced lung injury were investigated through histological examination, ELISA, qRT-PCR, Western blot and immunofluorescence. In vitro, human lung microvascular endothelial cells (HPMECs) were employed to understand the protective effects of UDCA. The extent of ALI/ARDS was evaluated and validated by reduced PaO /FiO ratios, increased lung wet/dry (W/D) ratios and impaired alveolar-capillary barrier, up-regulation of ALI-related proteins in lung tissues (including myeloperoxidase [MPO], vascular cell adhesion molecule 1 [VCAM-1], intercellular cell adhesion molecule-1 [ICAM-1]), elevated protein concentration and increased proinflammatory cytokines levels (TNF-α and IL-1β) in bronchoalveolar lavage fluid (BALF). Pre-treatment with UDCA remarkably alleviated these pathologic and biochemical changes of FES-induced ALI/ARDS; our data demonstrated that pre-treatment with UDCA attenuated the pathologic and biochemical changes of FES-induced ARDS, which provided a possible preventive therapy for lung injury caused by FES.

摘要

急性肺损伤(ALI)/急性呼吸窘迫综合征(ARDS)是一种死亡率很高的危及生命的疾病,它曾是脂肪栓塞综合征(FES)的常见并发症。据报道,熊去氧胆酸(UDCA)在各种情况下都具有强大的抗炎作用。在体内,通过尾静脉注射肾周脂肪以建立大鼠FES模型,通过组织学检查、酶联免疫吸附测定(ELISA)、定量逆转录聚合酶链反应(qRT-PCR)、蛋白质免疫印迹法(Western blot)和免疫荧光法研究UDCA对FES诱导的肺损伤的抗炎作用。在体外,用人肺微血管内皮细胞(HPMECs)来了解UDCA的保护作用。通过降低的动脉血氧分压/吸入氧分数(PaO₂/FiO₂)比值、升高的肺湿/干(W/D)比值和受损的肺泡-毛细血管屏障、肺组织中ALI相关蛋白(包括髓过氧化物酶[MPO]、血管细胞黏附分子1[VCAM-1]、细胞间黏附分子-1[ICAM-1])的上调、支气管肺泡灌洗液(BALF)中蛋白质浓度升高和促炎细胞因子水平(肿瘤坏死因子-α[TNF-α]和白细胞介素-1β[IL-1β])升高来评估和验证ALI/ARDS的程度。用UDCA预处理可显著减轻FES诱导的ALI/ARDS的这些病理和生化变化;我们的数据表明,用UDCA预处理可减轻FES诱导的ARDS的病理和生化变化,这为FES引起的肺损伤提供了一种可能的预防性治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/44e6/7754031/1f5bd31ab254/JCMM-24-14626-g001.jpg

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