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高渗盐水通过抑制水通道蛋白4的表达减轻脂多糖诱导的小鼠脑水肿。

Hypertonic saline reduces lipopolysaccharide-induced mouse brain edema through inhibiting aquaporin 4 expression.

作者信息

Cao C, Yu X, Liao Z, Zhu N, Huo H, Wang M, Ji G, She H, Luo Z, Yue S

出版信息

Crit Care. 2012 Oct 4;16(5):R186. doi: 10.1186/cc11670.

DOI:10.1186/cc11670
PMID:23036239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3682288/
Abstract

INTRODUCTION

Three percent sodium chloride (NaCl) treatment has been shown to reduce brain edema and inhibited brain aquaporin 4 (AQP4) expression in bacterial meningitis induced by Escherichia coli. Lipopolysaccharide (LPS) is the main pathogenic component of E. coli. We aimed to explore the effect of 3% NaCl in mouse brain edema induced by LPS, as well as to elucidate the potential mechanisms of action.

METHODS

Three percent NaCl was used to treat cerebral edema induced by LPS in mice in vivo. Brain water content, IL-1β, TNFα, immunoglobulin G (IgG), AQP4 mRNA and protein were measured in brain tissues. IL-1β, 3% NaCl and calphostin C (a specific inhibitor of protein kinase C) were used to treat the primary astrocytes in vitro. AQP4 mRNA and protein were measured in astrocytes. Differences in various groups were determined by one-way analysis of variance.

RESULTS

Three percent NaCl attenuated the increase of brain water content, IL-1β, TNFα, IgG, AQP4 mRNA and protein in brain tissues induced by LPS. Three percent NaCl inhibited the increase of AQP4 mRNA and protein in astrocytes induced by IL-1β in vitro. Calphostin C blocked the decrease of AQP4 mRNA and protein in astrocytes induced by 3% NaCl in vitro.

CONCLUSIONS

Osmotherapy with 3% NaCl ameliorated LPS-induced cerebral edema in vivo. In addition to its osmotic force, 3% NaCl exerted anti-edema effects possibly through down-regulating the expression of proinflammatory cytokines (IL-1β and TNFα) and inhibiting the expression of AQP4 induced by proinflammatory cytokines. Three percent NaCl attenuated the expression of AQP4 through activation of protein kinase C in astrocytes.

摘要

引言

已证实3%氯化钠(NaCl)治疗可减轻大肠杆菌所致细菌性脑膜炎的脑水肿并抑制脑水通道蛋白4(AQP4)表达。脂多糖(LPS)是大肠杆菌的主要致病成分。我们旨在探讨3% NaCl对LPS诱导的小鼠脑水肿的影响,并阐明其潜在作用机制。

方法

采用3% NaCl对体内LPS诱导的小鼠脑水肿进行治疗。检测脑组织中的脑含水量、白细胞介素-1β(IL-1β)、肿瘤坏死因子α(TNFα)、免疫球蛋白G(IgG)、AQP4 mRNA和蛋白。体外使用IL-1β、3% NaCl和钙泊三醇(蛋白激酶C的特异性抑制剂)处理原代星形胶质细胞。检测星形胶质细胞中的AQP4 mRNA和蛋白。通过单因素方差分析确定各组间差异。

结果

3% NaCl减轻了LPS诱导的脑组织中脑含水量、IL-1β、TNFα、IgG、AQP4 mRNA和蛋白的增加。3% NaCl在体外抑制了IL-1β诱导的星形胶质细胞中AQP4 mRNA和蛋白的增加。钙泊三醇在体外阻断了3% NaCl诱导的星形胶质细胞中AQP4 mRNA和蛋白的减少。

结论

3% NaCl渗透疗法改善了体内LPS诱导的脑水肿。除渗透作用外,3% NaCl可能通过下调促炎细胞因子(IL-1β和TNFα)的表达以及抑制促炎细胞因子诱导的AQP4表达发挥抗水肿作用。3% NaCl通过激活星形胶质细胞中的蛋白激酶C减轻AQP4的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/499b12304455/cc11670-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/8dfe13721e99/cc11670-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/263010cf460c/cc11670-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/979264b78eaf/cc11670-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/accb50716575/cc11670-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/a956887a78d1/cc11670-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/499b12304455/cc11670-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/8dfe13721e99/cc11670-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/263010cf460c/cc11670-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/979264b78eaf/cc11670-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/accb50716575/cc11670-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/a956887a78d1/cc11670-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ac17/3682288/499b12304455/cc11670-6.jpg

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