Renata Salatti Ferrari1,a, Leonardo Dalla Giacomassa Rocha Thomaz2,b, Lucas Elias Lise Simoneti2,c, Jane Maria Ulbrich1,3,d, Cristiano Feijó Andrade1,3,e
ABSTRACT
Liquid perfluorocarbon (PFC) instillation has been studied experimentally as an adjuvant therapy in the preservation of lung grafts during cold ischemia. The objective of this study was to evaluate whether vaporized PFC is also protective of lung grafts at different cold ischemia times. We performed histological analysis of and measured oxidative stress in the lungs of animals that received only preservation solution with low-potassium dextran (LPD) or vaporized PFC together with LPD. We conclude that vaporized PFC reduces the production of free radicals and the number of pulmonary structural changes resulting from cold ischemia.
Keywords: Ischemia; Reperfusion; Fluorocarbons; Lung transplantation; Oxidative stress.
RESUMO
O perfluorocarbono (PFC) líquido tem sido estudado experimentalmente como uma substância adjuvante na preservação de enxertos pulmonares durante o período de isquemia fria. O objetivo deste estudo foi avaliar se o PFC vaporizado (e não instilado) também atuaria como protetor de enxertos pulmonares em diferentes tempos de isquemia fria. Realizamos análise histológica e dosamos o estresse oxidativo em pulmões de animais que receberam somente uma solução de preservação com low-potassium dextran (LPD, dextrana com baixa concentração de potássio) ou PFC vaporizado associado a LPD. Concluímos que o PFC vaporizado reduziu a produção de radicais livres e provocou menor número de alterações estruturais pulmonares decorrentes do período de isquemia fria que o uso de LPD isoladamente.
Palavras-chave: Isquemia; Reperfusão; Fluorcarbonetos; Transplante de pulmão; Estresse oxidativo.
Various methods and substances to improve lung graft preservation during cold ischemia, such as pulmonary surfactant, liquid perfluorocarbon (PFC), complement inhibitors, and nitrites, as well as inhalation of hydrogen sulfide or nitric oxide, have been tested experimentally.(1,2) However, the standard method of lung graft preservation is still perfusion with a cold low-potassium dextran (LPD) solution via the pulmonary artery (antegrade perfusion) or via the pulmonary veins (retrograde perfusion), together with the use of pulmonary vasodilators and partial inflation of the lungs with oxygen during storage. (2) The use of vaporized PFC seems to be an interesting alternative in lung graft preservation, given that the use of liquid PFC has been shown to be protective of lung grafts before and after reperfusion.(3-5) The potential benefits of vaporized PFC in lung graft preservation are its ability to transport oxygen and carbon dioxide, together with its anti-inflammatory and antioxidant properties.(6-8) In addition, in its vaporized form, PFC is easily distributed throughout the lungs in a more uniform way, and, chiefly, it does not cause the ventilation difficulties observed in lungs perfused with liquid PFC. To determine the effects of vaporized PFC during lung graft preservation and to analyze oxidative stress/histological changes in lung grafts preserved for different periods of time, we used an animal model of cold ischemia. This was a controlled experimental study involving Wistar rats with a mean body weight of 300 g. All animals were treated in accordance with the World Health Organization Code of Ethics for Animal Experimentation. The animals were divided into two groups, each of which was subdivided into four groups. Each subgroup comprised six animals, depending on the surgical procedure: PFC + LPD 3h; PFC + LPD 6h; PFC + LPD 12h; and PFC + LPD 24h subgroups vs. LPD 3h; LPD 6h; LPD 12h; and LPD 24h. In the four PFC + LPD subgroups, regardless of preservation time, we used a dose of 7 mL/kg of vaporized PFC, through a tracheotomy cannula connected to an anesthesia machine, after a 120-min period of reperfusion. The animals were killed after anesthesia with ketamine (100 mg/kg, i.p.) and xylazine (50 mg/kg). Subsequently, a mid-ventral laparotomy was performed. The lungs were removed and fixed in 4% paraformaldehyde for histological analysis and were stored at −80°C for subsequent quantification of thiobarbituric acid reactive substances (TBARS), as well as for evaluation of the activity of the enzymes superoxide dismutase (SOD) and catalase. For biochemical analysis, the lung tissue was homogenized, after which protein levels were quantified as proposed by Lowry et al.(9) The levels of TBARS were measured as described by Buege and Aust,(10) and SOD activity was determined according to the technique described by Misra and Fridovich. (11) Catalase activity was analyzed by measuring the reduction in hydrogen peroxide levels.(12) The lung tissue samples for histological analysis were collected and stored in 10% formaldehyde solution for 12 h, after which the solution was replaced with 70% alcohol and the samples were stained with H&E. All pathology studies were performed by a pathologist who was blinded to the subgroups. Data were analyzed with IBM SPSS Statistics software, version 22.0 (IBM Corporation, Armonk, NY, USA). ANOVA followed by Tukey's post hoc test was used; in cases of unequal variance or non-normal distribution, the nonparametric Kruskal-Wallis test was performed, followed by the Mann-Whitney U test for intergroup comparisons. For all comparisons, the level of significance was set at 5%. The lungs preserved with vaporized PFC (at a dose of 7 mL/kg) + LPD for 3 and 6 h showed significantly higher SOD concentrations than did those in the LPD 3h and LPD 6h subgroups, respectively. We found no significant differences in TBARS or catalase levels among the subgroups (Figure 1).