乳化七氟醚和乌司他丁对胆管结扎大鼠肝、肺损伤的影响

Chen Cai-Yang, Zhu Ming, W. Long, Wu Feixiang, Yang Li-qun, Yuan Weifeng
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引用次数: 1

摘要

背景:探讨乳化七氟醚和乌司他丁对梗阻性黄疸大鼠肝、肺损伤的影响及其机制。方法:雄性Sprague-Dawley大鼠随机分为两组进行体内研究。第一部分:假手术组、胆管结扎(BDL)组、BDL+脂质载体输注(BDL+V)组、BDL+乌司他丁(BDL+U)组、BDL+乳化七氟醚(BDL+E)组;通过总胆红素(TBIL)、丙氨酸转氨酶(ALT)和肺动脉血气分析检测肝功能和肺功能。肝和肺的损伤通过肝和肺样本的血红素和伊红(HE)染色进行组织学估计。免疫组化(IHC)检测活化巨噬细胞分子标志物F4/80。第二部分:Sham+氯化钆(GdCl3)基团、BDL+GdCl3基团、BDL+U+GdCl3基团、BDL+E+GdCl3基团。巨噬细胞缺失后,用HE染色对GdCl3处理大鼠的肝脏和肺部进行组织学检查。体外实验采用不同处理刺激RAW264.7细胞系,检测末端脱氧核苷酸转移酶dUTP nick end标记(TUNEL染色)、Hoechst 33342染色及凋亡相关基因的表达,进一步确定乌司他丁和乳化七氟醚的保护作用。结果:乳化七氟醚联合乌司他丁治疗可减轻胆汁淤积性肝、肺损伤,抑制肝、肺组织巨噬细胞活化,改善肝肺功能。它们还能抑制细胞凋亡途径。结论:乳化型七氟醚联合乌司他丁可改善bdl诱导的胆汁淤积性肝、肺损伤,其机制可能与巨噬细胞失活和细胞凋亡通路的调节有关。上述机制为多脏器损伤的围手术期治疗提供了新的途径。引用本文:陈彩阳,朱明,王龙,吴飞翔,杨利群,余卫峰。乳化液七氟醚和乌司他丁对胆管结扎大鼠肝肺损伤的影响。中华外科杂志2017;4: 7 - 16。doi: 10.24015/ japm .2017.0002这是一篇开放获取的文章,由Evidence Based Communications (EBC)发表。本作品遵循知识共享署名4.0国际许可协议,允许以任何媒介或格式出于任何合法目的不受限制地使用、分发和复制。要查看此许可证的副本,请访问http://creativecommons.org/licenses/by/4.0/。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of Emulsified Sevoflurane and Ulinastatin on Liver and Lung Injury Induced by Bile Duct Ligation in Rats
Backgroud: To investigate the effects and their mechanisms of emulsified sevoflurane and ulinastatin on liver and lung injury induced by obstructive jaundice in rats.Methods: For the in vivo study, male Sprague-Dawley rats were randomized into two parts. Part 1: Sham group, bile duct ligation (BDL) group, BDL and lipid vehicle infusion (BDL+V) group, BDL+ulinastatin (BDL+U) group, BDL+emulsified sevoflurane (BDL+E) group; Liver and lung function was examined by the concentrations of Total Bilirubin (TBIL), Alanine Transaminase (ALT), and lung arterial blood gas analysis. Liver and lung damage was estimated histologically with haematoxylin and eosin (HE) staining in liver and lung samples. F4/80, the molecular marker of activated macrophages, was assessed by immunohistochemistry (IHC). Part 2: Sham+Gadolinium chloride (GdCl3)group, BDL+GdCl3 group, BDL+U+GdCl3 group, BDL+E+GdCl3 group. After the deletion of macrophages, liver and lung examinations were evaluated histologically with HE staining in GdCl3 treated rats. For the in vitro study, the RAW264.7 cell line was stimulated by the different treatments, then terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL staining), Hoechst 33342 staining and the expressions of apoptotic related genes were evaluated to further determine the protective effects of ulinastatin and emulsified sevoflurane.Results: Emulsified sevoflurane and ulinastatin therapies alleviated cholestatic liver and lung damage, inhibited the activation of macrophages in the liver and lung tissues, and improved the liver and lung functions. And they were also found to inhibit apoptosis pathways.Conclusions: Emulsified sevoflurane and ulinastatin treatments were proved to ameliorate BDL-induced cholestatic liver and lung injuries, which were related to the inactivation of the macrophages and the regulation of apoptosis pathways. The above-mentioned mechanisms show new promising approach for the multi-organs injuries in the perioperative management. Citation: Cai-Yang Chen, Ming Zhu, Long Wang, Fei-Xiang Wu, Li-Qun Yang, Wei-Feng Yu. Effects of emulsified sevoflurane and ulinastatin on liver and lung injury induced by bile duct ligation in rats. J Anesth Perioper Med 2017; 4: 7-16. doi: 10.24015/JAPM.2017.0002This is an open-access article, published by Evidence Based Communications (EBC). This work is licensed under the Creative Commons Attribution 4.0 International License, which permits unrestricted use, distribution, and reproduction in any medium or format for any lawful purpose. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
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