Postgraduate Program in Pulmonology, Federal University of Rio Grande do Sul (UFRGS), 90040-060 Porto Alegre, RS, Brazil ; Methodist University (IPA), 906301-170 Porto Alegre, RS, Brazil ; Thoracic Surgery Department, Laboratory of Airways and Lung, Hospital de Clínicas de Porto Alegre (HCPA), Ramiro Barcelos 2.350, 90035-903 Porto Alegre, RS, Brazil.
Thoracic Surgery Department, Laboratory of Airways and Lung, Hospital de Clínicas de Porto Alegre (HCPA), Ramiro Barcelos 2.350, 90035-903 Porto Alegre, RS, Brazil.
Mediators Inflamm. 2013;2013:193484. doi: 10.1155/2013/193484. Epub 2013 Dec 26.
The aim of this study was to evaluate the use of liquid perfluorocarbon (PFC) as an adjuvant substance for lung preservation and assess its role in pulmonary protection after transplantation.
Seventy-two rat lungs were flushed with low-potassium dextran (LPD) solution and randomized into three main groups: control with LPD alone and experimental with 3 (PFC3) and 7 mL/kg (PFC7) of endobronchial PFC instilled just after harvest. Each group was divided into four subgroups according to preservation time (3, 6, 12, and 24 hours). Afterwards, we performed lung transplantation using rat lungs preserved for 12 hours with LPD alone or with 7 mL/kg of endobronchial PFC.
There was a significant increase in oxidative stress in the control group at 6 h of cold ischemic time compared with the PFC3 and PFC7 groups. The apoptotic activity and NF-κB expression were significantly higher in the control group compared with the PFC groups at 3, 12, and 24 h of cold preservation. After transplantation, the NF-κB, iNOS, and nitrotyrosine expression as well as caspase 3 activity were significantly lower in the PFC groups.
The use of endobronchial PFC as an adjuvant to the current preservation strategy improved graft viability.
本研究旨在评估液体全氟碳(PFC)作为肺保护辅助物质的应用,并评估其在移植后肺保护中的作用。
72 个大鼠肺用低钾右旋糖酐(LPD)溶液冲洗,随机分为三组:单纯 LPD 对照组,支气管内注入 3(PFC3)和 7 毫升/公斤(PFC7)的实验组。每组根据保存时间(3、6、12 和 24 小时)进一步分为四个亚组。然后,我们使用 LPD 单独或支气管内注入 7 毫升/公斤的 PFC 保存 12 小时的大鼠肺进行肺移植。
与 PFC3 和 PFC7 组相比,对照组在冷缺血 6 小时时氧化应激明显增加。与 PFC 组相比,对照组在冷保存 3、12 和 24 小时时凋亡活性和 NF-κB 表达明显升高。移植后,PFC 组 NF-κB、iNOS 和硝基酪氨酸表达以及 caspase 3 活性明显降低。
支气管内 PFC 的使用作为当前保存策略的辅助手段提高了移植物的活力。