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地塞米松联合环丙沙星通过糖皮质激素(GC)-GC 受体介导途径调节金黄色葡萄球菌诱导的小胶质细胞炎症。

Dexamethasone along with ciprofloxacin modulates S. aureus induced microglial inflammation via glucocorticoid (GC)-GC receptor-mediated pathway.

机构信息

Department of Physiology, Immunology Laboratory, University of Calcutta, University Colleges of Science and Technology, Calcutta, West Bengal, India.

Department of Physiology, Immunology Laboratory, University of Calcutta, University Colleges of Science and Technology, Calcutta, West Bengal, India.

出版信息

Microb Pathog. 2020 Aug;145:104227. doi: 10.1016/j.micpath.2020.104227. Epub 2020 Apr 28.

Abstract

Microglial inflammation is the hallmark of S. aureus induced brain abscesses. Conventional antibiotic therapy could not regulate inflammation and the use of steroids in CNS infection remained controversial. To address this issue the effect of dexamethasone along with ciprofloxacin on microglial inflammation has been attempted both in glucocorticoid receptor (GR) opened and blocked condition. We have investigated the effects of ciprofloxacin (0.24 μg/ml, pre-treatment) and dexamethasone (150 nM, pre-treatment) in combination with murine microglia infected with S. aureus for 30, 60 and 90 min by either keeping GR opened or blocked with GR antagonist RU486. Alterations in cellular motility, intracellular killing assay, free radical production, antioxidant enzyme activities, corticosterone, and cytokine levels were determined. The expressions of TLR-2, GR, and other inflammatory markers were determined in terms of this combinatorial treatment. Combination treatment significantly (p < 0.05) reduced the bacterial burden of microglia only when GR remained open and effectively suppressed S. aureus induced oxidative stress by augmenting SOD and catalase enzyme activity and suppressing other pro-inflammatory markers at 90 min. Arginase activity, a critical determinant of microglial polarization was found to be higher after treatment at 60 and 90 min. This situation was reversed when this combination treatment was applied by keeping GR blocked using GR antagonist RU486. Therefore, it can be concluded that combination treatment of ciprofloxacin and dexamethasone could regulate S. aureus induced microglial activation, in the presence of functional GR via utilizing glucocorticoid (GC)-GR pathway and ultimately confers protection to the host from brain inflammation.

摘要

小胶质细胞炎症是金黄色葡萄球菌诱导脑脓肿的标志。常规抗生素治疗不能调节炎症,皮质类固醇在中枢神经系统感染中的应用仍存在争议。为了解决这个问题,尝试了在糖皮质激素受体(GR)开放和阻断的情况下,地塞米松与环丙沙星联合对小胶质细胞炎症的作用。我们研究了环丙沙星(0.24μg/ml,预处理)和地塞米松(150nM,预处理)与金黄色葡萄球菌感染的小鼠小胶质细胞联合使用 30、60 和 90min 的效果,通过保持 GR 开放或用 GR 拮抗剂 RU486 阻断 GR。测定细胞迁移、细胞内杀伤试验、自由基产生、抗氧化酶活性、皮质酮和细胞因子水平的变化。根据这种组合治疗,测定了 TLR-2、GR 和其他炎症标志物的表达。当 GR 保持开放时,联合治疗显著(p<0.05)降低了小胶质细胞中的细菌负荷,并通过增强 SOD 和过氧化氢酶酶活性和抑制其他促炎标志物在 90min 时有效地抑制了金黄色葡萄球菌诱导的氧化应激。发现 60 和 90min 后处理后,精氨酸酶活性(小胶质细胞极化的关键决定因素)更高。当使用 GR 拮抗剂 RU486 阻断 GR 时,这种联合治疗可以逆转这种情况。因此,可以得出结论,环丙沙星和地塞米松的联合治疗可以通过利用糖皮质激素(GC)-GR 途径调节金黄色葡萄球菌诱导的小胶质细胞激活,在功能 GR 的存在下,最终使宿主免受脑炎症的侵害。

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