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致命性糖尿病酮症酸中毒时脉络丛上皮的神经炎症反应。

Neuroinflammatory response of the choroid plexus epithelium in fatal diabetic ketoacidosis.

作者信息

Hoffman William H, Casanova Manuel F, Cudrici Cornelia D, Zakranskaia Ekaterina, Venugopalan Roopa, Nag Sukriti, Oglesbee Michael J, Rus Horea

机构信息

Department of Pediatrics, Medical College of Georgia, Augusta, GA 30912, USA.

出版信息

Exp Mol Pathol. 2007 Aug;83(1):65-72. doi: 10.1016/j.yexmp.2007.01.006. Epub 2007 Jan 30.

Abstract

A systemic inflammatory response (SIR) occurs prior to and during the treatment of severe diabetic ketoacidosis (DKA). IL-1beta, TNF-alpha and C5b-9 are components of SIR and have been speculated to be involved in the clinical brain edema (BE) of DKA. We studied IL-1beta, TNF-alpha, C5b-9, inducible nitric oxide (iNOS), ICAM-1, IL-10 and Hsp70 expression in the brains of two patients who died as the result of clinical BE during the treatment of DKA. IL-1beta was strongly expressed in the choroid plexus epithelium (CPE) and ependyma, and to a lesser extent in the hippocampus, caudate, white matter radiation of the pons, molecular layer of the cerebellum and neurons of the cortical gray matter. TNF-alpha was expressed to a lesser extent than IL-1beta, and only in the CP. C5b-9, previously shown to be deposited on neurons and oligodendrocytes, was found on CPE and ependymal cells. iNOS and ICAM-1 had increased expression in the CPE and ependyma. Hsp70 and IL-10 were also expressed in the CPE of the case with the shorter duration of treatment. Our data demonstrate the presence of a multifaceted neuroinflammatory cytotoxic insult of the CPE, which may play a role in the pathophysiology of the fatal brain edema of DKA.

摘要

在严重糖尿病酮症酸中毒(DKA)治疗之前及治疗期间会发生全身炎症反应(SIR)。白细胞介素-1β(IL-1β)、肿瘤坏死因子-α(TNF-α)和C5b-9是SIR的组成部分,据推测它们与DKA的临床脑水肿(BE)有关。我们研究了两名在DKA治疗期间因临床BE死亡患者大脑中IL-1β、TNF-α、C5b-9、诱导型一氧化氮合酶(iNOS)、细胞间黏附分子-1(ICAM-1)、白细胞介素-10(IL-10)和热休克蛋白70(Hsp70)的表达情况。IL-1β在脉络丛上皮(CPE)和室管膜中强烈表达,在海马体、尾状核、脑桥白质辐射区、小脑分子层和皮质灰质神经元中的表达程度较低。TNF-α的表达程度低于IL-1β,且仅在脉络丛中表达。先前已证明C5b-9沉积在神经元和少突胶质细胞上,在本研究中发现其存在于CPE和室管膜细胞上。iNOS和ICAM-1在CPE和室管膜中的表达增加。在治疗时间较短的病例的CPE中也表达了Hsp70和IL-10。我们的数据表明存在对CPE的多方面神经炎性细胞毒性损伤,这可能在DKA致命脑水肿的病理生理学中起作用。

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