Meisel Christian, Prass Konstantin, Braun Johann, Victorov Ilya, Wolf Tilo, Megow Dirk, Halle Elke, Volk Hans-Dieter, Dirnagl Ulrich, Meisel Andreas
Medical Immunology, Medical Faculty Charité, Humboldt-University, Berlin, Germany.
Stroke. 2004 Jan;35(1):2-6. doi: 10.1161/01.STR.0000109041.89959.4C. Epub 2003 Dec 18.
Epidemiological studies have demonstrated a high incidence of infections after severe stroke and their prominent role in morbidity and mortality in stroke patients. In a mouse model, it has been shown recently that stroke is coupled with severe and long-lasting immunosuppression, which is responsible for the development of spontaneous systemic infections. Here, we investigated in the same model the effects of preventive antibiotic treatment on survival and functional outcome of experimental stroke.
Mice were subjected to experimental stroke by occlusion of the middle cerebral artery (MCAO) for 60 minutes. A group of mice received moxifloxacin (6x100 mg/kg body weight every 2 hours over 12 hours) either immediately or 12 hours after MCAO. Control animals received the vector only. Behavior, neurological deficit, fever, survival, and body weight were monitored over 14 days. In a subgroup, infarct volume was measured 4 days after MCAO. Microbiological assessment was based on cultures of lung tissue, blood, and feces of animals 3 days after stroke. For a dose-response study, moxifloxacin was given immediately after MCAO in different doses and at different time points.
Microbiological analyses of blood and lung tissue demonstrated high bacterial burden, mainly Escherichia coli, 3 days after stroke. Accordingly, we observed clinical and histological signs of septicemia and pneumonia. Moxifloxacin prevented the development of infections and fever, significantly reduced mortality, and improved neurological outcome.
Preventive antibiotic treatment may be an important new therapeutical approach to improve outcome in patients with severe stroke.
流行病学研究表明,重症卒中后感染的发生率很高,且在卒中患者的发病率和死亡率中起着重要作用。在小鼠模型中,最近研究发现卒中与严重且持久的免疫抑制相关,这是导致自发性全身感染的原因。在此,我们在同一模型中研究了预防性抗生素治疗对实验性卒中的生存率和功能结局的影响。
通过大脑中动脉闭塞(MCAO)60分钟使小鼠发生实验性卒中。一组小鼠在MCAO后立即或12小时接受莫西沙星(每2小时6×100mg/kg体重,共12小时)治疗。对照动物仅接受载体。在14天内监测行为、神经功能缺损、发热、生存率和体重。在一个亚组中,MCAO后4天测量梗死体积。微生物学评估基于卒中后3天动物的肺组织、血液和粪便培养。为了进行剂量反应研究,在MCAO后立即以不同剂量和不同时间点给予莫西沙星。
血液和肺组织的微生物学分析显示,卒中后3天细菌负荷很高,主要为大肠杆菌。相应地,我们观察到败血症和肺炎的临床及组织学迹象。莫西沙星可预防感染和发热的发生,显著降低死亡率,并改善神经功能结局。
预防性抗生素治疗可能是改善重症卒中患者结局的一种重要的新治疗方法。