Pacheco Eduardo Garcia, Gomes Maria Cecília Jordani, Rodrigues Gustavo Ribeiro, Campos Walter, Kemp Rafael, Silva Orlando de Castro e
Division of Gastroenterology, Department of Surgery and Anatomy, FMRP, USP, Brazil.
Acta Cir Bras. 2006;21 Suppl 1:24-8. doi: 10.1590/s0102-86502006000700006.
The main aim of this study was to determine the influence of ischemic preconditioning (IPC) on rat liver cirrhosis.
Cirrhosis was induced in Wistar rats by occlusion of the hepatic duct. The animals were divided into four groups of six animals each: non-cirrhotic group (simulated operation only), cirrhotic control group (simulated operation in cirrhotic rats), I/R group (40-minute ischemia without IPC), and IPC group (cirrhotic rats with ischemia, previously submitted to IPC). The IPC procedure consisted of partial hepatic ischemia for five minutes, followed by 10 minutes of reperfusion. In the case of the IPC group, the animals were submitted to liver ischemia for 40 minutes after the preconditioning procedure, followed by 2 hours of reperfusion. Blood samples were collected for measurement of serum aminotransferases (ALT and AST). The respiratory control ratio (RCR), the mitochondrial membrane potential (MMP), and malondialdehyde (MDA) values in the hepatic tissue were analyzed. Nonparametric statistical analysis was used and a value of p<0.05 was considered statistically significant.
Ischemia did not induce significant increase in ALT and AST levels. MDA values were significantly higher in cirrhotic animals. MMP did not significantly change in cirrhosis and liver ischemia. Mitochondrial RCR decreased in liver cirrhosis, accentuated upon liver ischemia, and did not significantly change with IPC.
Ischemic preconditioning does not protect the liver from hepatic injury induced by the ischemia/reperfusion process.
本研究的主要目的是确定缺血预处理(IPC)对大鼠肝硬化的影响。
通过闭塞肝管在Wistar大鼠中诱导肝硬化。将动物分为四组,每组六只动物:非肝硬化组(仅模拟手术)、肝硬化对照组(肝硬化大鼠模拟手术)、I/R组(40分钟缺血,无IPC)和IPC组(缺血的肝硬化大鼠,先前进行过IPC)。IPC程序包括部分肝缺血5分钟,然后再灌注10分钟。对于IPC组,动物在预处理程序后进行40分钟的肝脏缺血,然后再灌注2小时。采集血样以测量血清转氨酶(ALT和AST)。分析肝组织中的呼吸控制率(RCR)、线粒体膜电位(MMP)和丙二醛(MDA)值。采用非参数统计分析,p<0.05的值被认为具有统计学意义。
缺血未引起ALT和AST水平显著升高。肝硬化动物的MDA值显著更高。MMP在肝硬化和肝脏缺血中无显著变化。肝硬化时线粒体RCR降低,肝脏缺血时加剧,IPC后无显著变化。
缺血预处理不能保护肝脏免受缺血/再灌注过程诱导的肝损伤。