Takeyoshi Izumi, Yoshinari Daisuke, Kobayashi Mitsunobu, Kurabayashi Makoto, Morishita Yasuo
Second Department of Surgery, Gunma University School of Medicine, Maebashi, Japan.
Hepatogastroenterology. 2005 Sep-Oct;52(65):1507-10.
BACKGROUND/AIMS: Endotoxin shock induces multiple organ dysfunction syndromes that are associated with a substantial increase in mortality. In this study, we evaluated the effect of FR167653, a potent suppressant of tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 (IL-1) production, on lipopolysaccharide (LPS)-induced liver and kidney injury and lethality in rats.
Male Sprague-Dawley rats weighing from 200 to 270g received an injection of LPS. The FR group received an infusion of FR167653 at 0.2 mg/kg/hr, commencing 30 min prior to the LPS injection and continuing for 5.5 hr, while the control group received an infusion of a vehicle in the same fashion. Separate groups of animals were used for the survival study (n=5 each), and for blood sampling (n=5 each group, each time point).
The FR group showed a significantly better survival rate'than the control group. Serum levels of GOT, Cr, and BUN were significantly lower in the FR group than in the control group. The elevation of TNF-alpha and IL-1beta at 2 hr after LPS administration was significantly lower in the FR group than in the control group.
FR167653 administration is effective in decreasing serum TNF-alpha and IL-1beta levels and associated injury to liver and kidney caused by LPS-induced endotoxemia, as well as decreasing mortality.
背景/目的:内毒素休克可诱发多器官功能障碍综合征,这与死亡率大幅上升相关。在本研究中,我们评估了强效肿瘤坏死因子-α(TNF-α)和白细胞介素-1(IL-1)生成抑制剂FR167653对脂多糖(LPS)诱导的大鼠肝损伤、肾损伤及致死率的影响。
体重200至270克的雄性Sprague-Dawley大鼠注射LPS。FR组在LPS注射前30分钟开始以0.2毫克/千克/小时的速度输注FR167653,并持续5.5小时,而对照组以相同方式输注溶媒。分别使用不同组动物进行生存研究(每组n = 5)和采血(每组n = 5,每个时间点)。
FR组的生存率显著高于对照组。FR组血清谷草转氨酶(GOT)、肌酐(Cr)和尿素氮(BUN)水平显著低于对照组。LPS给药后2小时,FR组TNF-α和IL-1β的升高显著低于对照组。
给予FR167653可有效降低血清TNF-α和IL-1β水平,减轻LPS诱导的内毒素血症所致的肝、肾损伤,并降低死亡率。