Chrysikos Dimosthenis T, Sergentanis Theodoros N, Zagouri Flora, Psaltopoulou Theodora, Theodoropoulos George, Flessas Ioannis, Agrogiannis George, Alexakis Nikolaos, Lymperi Maria, Katsarou Ageliki I, Patsouris Efstratios S, Zografos Constantine G, Papalois Apostolos E
Department of Propaedeutic Surgery, Hippokratio Hospital. Athens, Greece.
JOP. 2015 Mar 20;16(2):176-84. doi: 10.6092/1590-8577/2952.
The potential of lazaroid U-74389G in attenuating injury after ischemia and reperfusion has been reported in various organs.
The present study focuses specifically on the pancreas and aims to examine any effects of U-74389G in a swine model of pancreatic ischemia and reperfusion, encompassing ischemic preconditioning.
Twelve pigs, weighing 28-35 kg, were randomized into two experimental groups. Group A (control group, n=6): Two periods of ischemic preconditioning (5 min each) separated by a 5-min rest interval; then ischemia time 30 min and reperfusion for 120 min. Group B (n=6): the same as above, with U-74389G intravenous injection in the inferior vena cava immediately prior to the initiation of reperfusion. Blood sampling and pancreatic biopsies were conducted at 0, 30, 60, 90 and 120 min after reperfusion.
Repeated-measures ANOVA was undertaken to evaluate differences between the two study groups. No statistically significant differences were noted concerning the histopathological parameters in the control and therapy groups (P=0.563 for edema, P=0.241 for hemorrhage, P=0.256 for leukocyte infiltration, P=0.231 for acinar necrosis and P=0.438 for vacuolization). In accordance with the above, serum metabolic data (glucose, creatinine, urea, total and direct bilirubin, total calcium, amylase, lipase, SGOT/AST, SGPT/ALT, ALP, GGT, LDH, CRP, insulin) were not significantly different between the two groups; similarly, tumor necrosis factor-α values (P=0.705) and tissue malondialdehyde levels (P=0.628) did not differ between the two groups.
This swine model of pancreatic ischemia and reperfusion, encompassing preconditioning, indicates that U-74389G lazaroid does not seem to exert protective effects from pancreatic damage.
已报道类维生素E化合物U - 74389G在减轻各种器官缺血再灌注损伤方面的潜力。
本研究专门聚焦于胰腺,旨在研究U - 74389G在包含缺血预处理的猪胰腺缺血再灌注模型中的任何作用。
12头体重28 - 35千克的猪被随机分为两个实验组。A组(对照组,n = 6):两段缺血预处理(各5分钟),间隔5分钟休息期;然后缺血30分钟,再灌注120分钟。B组(n = 6):与上述相同,但在再灌注开始前立即经下腔静脉静脉注射U - 74389G。在再灌注后0、30、60、90和120分钟进行采血和胰腺活检。
采用重复测量方差分析评估两组间差异。对照组和治疗组在组织病理学参数方面未观察到统计学显著差异(水肿P = 0.563,出血P = 0.241,白细胞浸润P = 0.256,腺泡坏死P = 0.231,空泡形成P = 0.438)。据此,两组间血清代谢数据(葡萄糖、肌酐、尿素、总胆红素和直接胆红素、总钙、淀粉酶、脂肪酶、谷草转氨酶/天冬氨酸转氨酶、谷丙转氨酶/丙氨酸转氨酶、碱性磷酸酶、γ-谷氨酰转肽酶、乳酸脱氢酶、C反应蛋白、胰岛素)无显著差异;同样,两组间肿瘤坏死因子-α值(P = 0.705)和组织丙二醛水平(P = 0.628)也无差异。
这种包含预处理的猪胰腺缺血再灌注模型表明,类维生素E化合物U - 74389G似乎对胰腺损伤没有保护作用。