All authors: Department of Intensive Care Unit, Xiangya Hospital, Central South University, Changsha, Hunan Province, China.
Crit Care Med. 2014 Jan;42(1):e12-21. doi: 10.1097/CCM.0b013e3182a63b1a.
To determine the role of neuroglobin in the pathology of sepsis-associated encephalopathy and ascertain if neuroglobin has any protective effects against sepsis-associated encephalopathy.
Randomized laboratory animal study.
Research university animal laboratory.
Two hundred and forty adult male Sprague-Dawley rats.
Rats received cecal puncture and ligation (or sham) surgery to induce sepsis, then broken up into groups based on whether or not the rat developed sepsis-associated encephalopathy as determined by electroencephalograph and evoked potential recordings. The rats were then left untreated to examine the effect of sepsis-associated encephalopathy on neuroglobin, treated with a neuroglobin antisense nucleotide to block gene expression, or given hemin, a neuroglobin inducer.
Following sepsis induction, diagnosis, and treatment, the brains were analyzed for both gross and ultrastructural morphology. Also, neuronal neuroglobin immunoreactivity and apoptosis (via terminal uridine nucleotide end-labeling) were examined. Blood serum levels were then analyzed for neuroglobin, superoxide dismutase, and malondialdehyde levels. We determined that sepsis-associated encephalopathy induces damage evident when examining both gross and ultrastructural morphology, as well as induces neuronal neuroglobin expression. Also, blockade of neuroglobin expression via antisense treatment will exacerbate these pathological effects, while increasing neuroglobin levels via hemin will ameliorate them. Blood analysis found that levels of superoxide dismutase and malondialdehyde mirrored the level of pathology found in the brain, while plasma neuroglobin levels reflected the amount of neuronal neuroglobin immunoreactivity.
We conclude that neuroglobin is involved in the pathogenesis of sepsis-associated encephalopathy and has neuroprotective effects. We also determined that hemin has protective effects against sepsis-associated encephalopathy as well, most probably due to its effect on neuroglobin.
确定神经球蛋白在脓毒症相关性脑病病理中的作用,并确定神经球蛋白是否对脓毒症相关性脑病具有保护作用。
随机实验室动物研究。
研究型大学动物实验室。
240 只成年雄性 Sprague-Dawley 大鼠。
大鼠接受盲肠穿刺和结扎(或假手术)手术以诱导脓毒症,然后根据脑电图和诱发电位记录确定是否发生脓毒症相关性脑病将大鼠分为不同组。然后,不进行治疗以检查脓毒症相关性脑病对神经球蛋白的影响,用神经球蛋白反义核苷酸阻断基因表达,或用血红素,一种神经球蛋白诱导剂进行治疗。
在诱导、诊断和治疗后,对大脑进行大体和超微结构形态分析。还检查了神经元神经球蛋白免疫反应和细胞凋亡(通过末端尿嘧啶核苷酸末端标记法)。然后分析血清中的神经球蛋白、超氧化物歧化酶和丙二醛水平。我们确定脓毒症相关性脑病可诱导明显的损伤,无论是在大体还是超微结构形态上都可观察到,并且诱导神经元神经球蛋白表达。此外,通过反义处理阻断神经球蛋白的表达会加剧这些病理效应,而通过血红素增加神经球蛋白水平则会改善这些效应。血液分析发现超氧化物歧化酶和丙二醛的水平与大脑中发现的病理水平相对应,而血浆神经球蛋白水平反映了神经元神经球蛋白免疫反应的量。
我们得出结论,神经球蛋白参与脓毒症相关性脑病的发病机制并具有神经保护作用。我们还确定血红素对脓毒症相关性脑病也具有保护作用,这很可能是由于其对神经球蛋白的作用。