Yildiz H, Coskuner I, Bulbuloglu E, Silay E, Kurutas E B, Dogan Z, Kantarceken B, Oksuz H, Senoglu N, Yuzbasioglu M F, Cetinkaya A, Ciralik H
Department of Anesthesiology, KSU, Kahramanmaras, Turkey.
Bratisl Lek Listy. 2012;113(3):139-44. doi: 10.4149/bll_2012_034.
In this study, we investigated the protective effects of frequently used intravenous anesthetics (ketamine, propofol, thiopental, and fentanyl) in oxidative stress in a rat liver model of obstructive jaundice.
Thirty-two Wistar albino rats were divided into four groups in a randomized fashion. All rats were subjected to laparotomy, common bile duct ligation and severance on day 0. Following 7 days, laparotomy was again performed using ketamine, propofol, pentobarbital, or fentanyl anesthesia. After 2 hours, the animals were sacrificed and tissue specimens were acquired for histopathological scoring and determination of malondialdehyde (MDA), superoxide dismutase (SOD) and catalase (CAT) activities.
All rats demonstrated enlargement in the bile duct, obstructive jaundice, and histopathologic ductal proliferation. MDA and SOD levels were significantly lower in the ketamine group compared with the thiopental and fentanyl groups. CAT was significantly increased in the ketamine group compared with the other groups. The best portal polymorphonuclear leukocyte and necrosis scores were in the ketamine group, but this difference was not statistically significant ( p=0.07).
Ketamine and propofol were observed to cause the least amount of oxidative stress in this rat model of induced oxidative stress generated by ligation of the common bile duct. This experiment is the first study on this subject in the literature (Tab. 3, Ref. 65).
在本研究中,我们在阻塞性黄疸大鼠肝脏模型中研究了常用静脉麻醉剂(氯胺酮、丙泊酚、硫喷妥钠和芬太尼)对氧化应激的保护作用。
32只Wistar白化大鼠随机分为四组。所有大鼠在第0天接受剖腹术、胆总管结扎和切断。7天后,再次使用氯胺酮、丙泊酚、戊巴比妥或芬太尼麻醉进行剖腹术。2小时后,处死动物并获取组织标本进行组织病理学评分以及测定丙二醛(MDA)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)活性。
所有大鼠均出现胆管扩张、阻塞性黄疸和组织病理学上的导管增生。氯胺酮组的MDA和SOD水平显著低于硫喷妥钠组和芬太尼组。氯胺酮组的CAT与其他组相比显著升高。氯胺酮组的门静脉多形核白细胞和坏死评分最佳,但差异无统计学意义(p = 0.07)。
在该由胆总管结扎诱导氧化应激的大鼠模型中,观察到氯胺酮和丙泊酚引起的氧化应激量最少。本实验是文献中关于该主题的首次研究(表3,参考文献65)。