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不同时间点给予乌司他丁对热射病大鼠肺组织病理形态的影响。

Effects of ulinastatin administered at different time points on the pathological morphologies of the lung tissues of rats with hyperthermia.

作者信息

Qin Zai-Sheng, Tian Pei, Wu Xia, Yu Hong-Mei, Guo Na

机构信息

Department of Anesthesiology, Nanfang Hospital, Southern Medical University, Guangzhou, Guangdong 510515, P.R. China.

出版信息

Exp Ther Med. 2014 Jun;7(6):1625-1630. doi: 10.3892/etm.2014.1656. Epub 2014 Apr 1.

DOI:10.3892/etm.2014.1656
PMID:24926355
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4043614/
Abstract

Hyperthermia not only directly induces cell injury of body tissues, but also causes the body to release large amounts of inflammatory mediators and cells with extensive biological activities to induce a systemic inflammatory response and immune dysfunction. Thus, hyperthermia causes systemic inflammatory response syndrome, aggravating injuries to various organs. This study aimed to observe the effects of ulinastatin (UTI) administered at different time points on the cellular morphologies of the lung tissues of rats with systemic hyperthermia. A total of 40 male Sprague Dawley rats were randomly divided into five groups: The normal control group (C group), the hyperthermia group without medication (H group), the hyperthermia and UTI pre-treatment group (HU group), the group treated with UTI at 1 h after hyperthermia (HU1 group), and the group treated with UTI at 2 h after hyperthermia (HU2 group). The systemic hyperthermia rat model was established in a heating chamber with a biological oxygen supply. For the HU, HU1 and HU2 groups, UTI (5×10 U/kg) was administered at different time points. For the C and H groups, an equivalent volume of normal saline was administered. During heating, the respiratory frequency and rectal temperature were measured and recorded once every 30 min. After 2.5 h of heating, the wet/dry weight (W/D) ratio of the lung tissues of the rats was measured. Additionally, the cellular morphologies of the lung tissues were observed under light and electron microscopes. The respiratory frequencies and lung tissue W/D ratios of the rats in the various hyperthermia groups were significantly higher than those of the rats in the C group (all P<0.05). The respiratory frequencies and lung tissue W/D values of the HU and HU1 groups were significantly lower than those of the H group (all P<0.05). Under the light microscope, the bronchial surrounding tissues of the HU and HU1 groups were loose, and the majority of the pulmonary alveolar structures were normal; the H and HU2 groups presented a number of changes, including pulmonary interstitial hyperemia, alveolar epithelial swelling and emphysema. Under the electron microscope, it was observed in the type II epithelial cells of the pulmonary alveoli of the H group that the mitochondria were swollen, the cell ridges were shortened, the microvilli were thin and increased, and the alveolar wall was thickened. Also, an increased number of infiltrating neutrophils were visible. In addition, the type II epithelial cells of the HU2 group also presented these changes to different extents and the changes in the HU and HU1 groups were the mildest. These results indicate that the early application of UTI relieves edema and the extent of cell injury of the lung tissue in rats with systemic hyperthermia.

摘要

高温不仅直接导致机体组织细胞损伤,还促使机体释放大量具有广泛生物活性的炎症介质和细胞,引发全身炎症反应和免疫功能紊乱。因此,高温导致全身炎症反应综合征,加重各器官损伤。本研究旨在观察不同时间点给予乌司他丁(UTI)对全身高温大鼠肺组织细胞形态的影响。将40只雄性Sprague Dawley大鼠随机分为五组:正常对照组(C组)、未用药高温组(H组)、高温与UTI预处理组(HU组)、高温后1小时给予UTI治疗组(HU1组)和高温后2小时给予UTI治疗组(HU2组)。在有生物供氧的加热箱中建立全身高温大鼠模型。对于HU组、HU1组和HU2组,在不同时间点给予UTI(5×10 U/kg)。对于C组和H组,给予等量生理盐水。加热过程中,每30分钟测量并记录呼吸频率和直肠温度。加热2.5小时后,测量大鼠肺组织的湿/干重(W/D)比值。此外,在光镜和电镜下观察肺组织的细胞形态。各高温组大鼠的呼吸频率和肺组织W/D比值均显著高于C组大鼠(均P<0.05)。HU组和HU1组的呼吸频率和肺组织W/D值均显著低于H组(均P<0.05)。光镜下,HU组和HU1组支气管周围组织疏松,多数肺泡结构正常;H组和HU2组出现一些变化,包括肺间质充血、肺泡上皮肿胀和肺气肿。电镜下,观察到H组肺泡Ⅱ型上皮细胞线粒体肿胀、细胞嵴缩短、微绒毛变细增多、肺泡壁增厚。此外,可见浸润中性粒细胞数量增加。另外,HU2组的Ⅱ型上皮细胞也有不同程度的这些变化,而HU组和HU1组的变化最轻。这些结果表明,早期应用UTI可减轻全身高温大鼠肺组织的水肿和细胞损伤程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/c7be269809d5/ETM-07-06-1625-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/265a64d3ecda/ETM-07-06-1625-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/e1ca5799aba7/ETM-07-06-1625-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/0cba36a0d771/ETM-07-06-1625-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/c7be269809d5/ETM-07-06-1625-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/265a64d3ecda/ETM-07-06-1625-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/e1ca5799aba7/ETM-07-06-1625-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/0cba36a0d771/ETM-07-06-1625-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23ec/4043614/c7be269809d5/ETM-07-06-1625-g03.jpg

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