Laboratory of Neurosciences and National Institute for Translational Medicine-INCT-TM, Postgraduate Program in Health Sciences, University of Southern Santa Catarina, Criciúma, SC 88806-000, Brazil.
J Neural Transm (Vienna). 2012 Nov;119(11):1267-74. doi: 10.1007/s00702-012-0774-2. Epub 2012 Feb 19.
Sepsis is characterized by systemic biochemical alterations including the central nervous system in the early times and cognitive impairment at later times after sepsis induction in the animal model. Recent studies have shown that, besides its hematological activity, erythropoietin (EPO) has cytoprotective effects on various cells and tissues. In order to corroborate elucidating the effects of alternative drugs for sepsis treatment, we evaluated the effects of both acute and chronic EPO treatment on oxidative stress and energetic metabolism in the hippocampus, and cognitive impairment, respectively, after sepsis induction by cecal ligation and perforation (CLP). To this aim, male Wistar rats underwent CLP with "basic support" or sham operation. In the acute treatment, EPO was administered once immediately after CLP induction. The rats were then killed after 6 and 24 h, and the hippocampus was removed for analysis of oxidative stress and energetic metabolism, respectively. Regarding the chronic treatment, EPO was administered once daily until the 4th day after induction. Aversive memory was tested on the 10th day after surgery. It was observed that the acute use of EPO (a single dose) alters the oxidative parameters and energetic metabolism. Chronic use (4 days) reversed cognitive impairment in the sepsis animal model. Mortality rates were attenuated only during chronic treatment.
败血症的特征是全身性生化改变,包括中枢神经系统在早期,以及在动物模型中败血症诱导后的后期认知障碍。最近的研究表明,除了其血液学活性外,促红细胞生成素(EPO)对各种细胞和组织具有细胞保护作用。为了证实对败血症治疗的替代药物的作用,我们评估了急性和慢性 EPO 治疗对败血症诱导后(CLP)海马中氧化应激和能量代谢的影响,以及认知障碍的影响。为此,雄性 Wistar 大鼠接受盲肠结扎和穿孔(CLP)手术或假手术。在急性治疗中,EPO 在 CLP 诱导后立即单次给药。然后在 6 和 24 小时后处死大鼠,并取出海马分析氧化应激和能量代谢。关于慢性治疗,EPO 每天给药一次,直到诱导后的第 4 天。术后第 10 天进行厌恶记忆测试。结果表明,EPO 的急性使用(单次剂量)改变了氧化参数和能量代谢。慢性使用(4 天)逆转了败血症动物模型中的认知障碍。只有在慢性治疗期间,死亡率才会降低。