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首页> 外文期刊>Brain research >Dexamethasone regulation of matrix metalloproteinase expression in experimental pneumococcal meningitis.
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Dexamethasone regulation of matrix metalloproteinase expression in experimental pneumococcal meningitis.

机译:地塞米松调节实验性肺炎球菌性脑膜炎中基质金属蛋白酶表达。

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摘要

Accumulating evidences have demonstrated that matrix metalloproteinases (MMPs) contribute to the pathophysiology of bacterial meningitis. MMPs facilitate leukocyte extravasation and brain edema by degradation of extracellular matrix components. Dexamethasone as adjunctive therapy to antibiotics has shown to have beneficial effects on pathophysiological changes and neurological outcome in children with meningitis and in animal models. However, the role of dexamethasone in the pathophysiology of pneumococcal meningitis is still unknown. The effects of antibiotics on MMPs in bacterial meningitis have not been evaluated so far. We have therefore intended to investigate the induction and expression of MMPs with special emphasis on the regulation of MMPs by dexamethasone and antibiotics in therapy of pneumococcal meningitis. In the present study, the expression of MMP-9 and MMP-2 mRNA in the brain of rats and the activity of MMP-9 and MMP-2 in the CSF of rats have been determined during the course of experimental bacterial meningitis and after treatment with an antibiotic plus dexamethasone. In the brain tissue of rats with Streptococcus pneumococcal meningitis, MMP-9 mRNA was obviously up-regulated after inoculation for 24 h (p<0.01) and then declined but was still greater than that in the brains of control rats after inoculation for 4 days (p<0.05) while the expression of MMP-2 remained at basal level. The expression of MMP-9 in the brains of rats inoculated with Streptococcus pneumoniae and treated by antibiotic was dose-dependent, up-regulated (p<0.01) but down-regulated after treatment with an antibiotic plus dexamethasone (p<0.01). However, the expression of MMP-9 mRNA did not change in the rats inoculated with sterile saline and treated with an antibiotic. The zymographic activity of MMP-9 and MMP-2 showed similar changes. The results indicated that the expression of MMP-9 mRNA and its activity might be increased after antibiotic treatment and inhibited after treatment with antibiotics plus dexamethasone; dexamethasone might have a beneficial effect on bacterial meningitis via down-regulation of the expression of MMP-9.
机译:越来越多的证据表明,基质金属蛋白酶(MMP)有助于细菌性脑膜炎的病理生理。 MMP通过降解细胞外基质成分促进白细胞外渗和脑水肿。地塞米松作为抗生素的辅助疗法已显示对脑膜炎患儿和动物模型的病理生理变化和神经系统结局具有有益作用。然而,地塞米松在肺炎球菌性脑膜炎的病理生理中的作用仍是未知的。迄今为止,尚未评估抗生素对细菌性脑膜炎中MMPs的影响。因此,我们打算研究MMPs的诱导和表达,特别强调地塞米松和抗生素在肺炎球菌性脑膜炎治疗中对MMPs的调节。本研究在实验性细菌性脑膜炎的过程中和治疗后,测定了大鼠脑中MMP-9和MMP-2 mRNA的表达以及脑脊液中MMP-9和MMP-2的活性。用抗生素加地塞米松。肺炎链球菌脑膜炎大鼠脑组织中,接种24 h后MMP-9 mRNA明显上调(p <0.01),然后下降,但仍高于对照大鼠接种4天后的脑组织。 (p <0.05),而MMP-2的表达仍处于基础水平。接种肺炎链球菌并经抗生素治疗的大鼠脑中MMP-9的表达呈剂量依赖性,上调(p <0.01),但经抗生素加地塞米松治疗后下调(p <0.01)。但是,在用无菌盐水接种并用抗生素处理的大鼠中,MMP-9 mRNA的表达没有变化。 MMP-9和MMP-2的酶活显示相似的变化。结果表明,抗生素处理后,MMP-9 mRNA的表达及其活性可能增加,而抗生素联合地塞米松处理后可能被抑制。地塞米松可能通过下调MMP-9的表达对细菌性脑膜炎产生有益作用。

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