Hacettepe University, Faculty of Medicine, Department of Physiology, Ankara, 06100, Turkey.
Prog Neuropsychopharmacol Biol Psychiatry. 2010 Dec 1;34(8):1440-5. doi: 10.1016/j.pnpbp.2010.07.034. Epub 2010 Aug 11.
Hepatic encephalopathy (HE) is a major neurological complication secondary to severe liver failure. The aim of the present study was to examine the possible neuroprotective effects of caffeic acid phenethyl ester (CAPE) with or without laxative treatment against thioacetamide-induced HE by investigating behavioral and motor activities in rats as well as blood ammonia level and oxidant-antioxidant parameters of cortex, brain stem and cerebellum. After induction of HE by thioacetamide, the rats were treated with lactulose, CAPE (CAPE treatment was started one day before the first dose of thioacetamide) or CAPE plus lactulose. The behavioral and motor scales were measured at the 54th hour after the first thioacetamide injection, the blood samples and brains were taken under anesthesia at the 60th hour for biochemical analysis. The survival rates were 37.5% in HE group, 70% in HE+lactulose group, 80% in HE+CAPE group, and 100% in HE+CAPE+lactulose group. Increased ammonia, ALT and AST levels in blood along with impaired sensory-motor behavior tests were reversed to proximate control values in CAPE+lactulose treated group. There were increased lipid peroxidation and protein oxidation and decreased antioxidant enzyme activities in almost all brain parts of HE group. CAPE or lactulose treatment alone ameliorated those oxidant and antioxidant parameters; however, CAPE treatment together with lactulose reversed them to almost control level. In conclusion, thioacetamide-induced HE injury in rats was reversed almost fully by CAPE and laxative combination. There was no death in CAPE and laxative treated group animals and it may be due to the direct neuroprotective effect of CAPE together with the prevention of the body from ammonia production.
肝性脑病(HE)是严重肝功能衰竭的主要神经系统并发症。本研究旨在通过研究大鼠的行为和运动活动以及皮质、脑干和小脑的血氨水平和氧化还原参数,探讨咖啡酸苯乙酯(CAPE)单独或联合泻药治疗对硫代乙酰胺诱导的 HE 的可能神经保护作用。在用硫代乙酰胺诱导 HE 后,用乳果糖、CAPE(CAPE 治疗在第一次硫代乙酰胺注射前一天开始)或 CAPE 加乳果糖治疗大鼠。在第一次硫代乙酰胺注射后 54 小时测量行为和运动量表,在 60 小时麻醉下取血样和大脑进行生化分析。HE 组的存活率为 37.5%,HE+乳果糖组为 70%,HE+CAPE 组为 80%,HE+CAPE+乳果糖组为 100%。血氨、ALT 和 AST 水平升高,感觉运动行为测试受损,在 CAPE+乳果糖治疗组恢复到接近对照值。HE 组几乎所有大脑部位的脂质过氧化和蛋白质氧化增加,抗氧化酶活性降低。CAPE 或乳果糖单独治疗可改善这些氧化和抗氧化参数;然而,CAPE 与乳果糖联合治疗可将其逆转至接近对照水平。总之,CAPE 和泻药的联合应用几乎完全逆转了硫代乙酰胺诱导的大鼠 HE 损伤。在 CAPE 和泻药治疗组的动物中没有死亡,这可能是由于 CAPE 的直接神经保护作用以及防止身体产生氨。