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右美托咪定治疗后对脂多糖诱导的星形胶质细胞炎症反应的影响。

The effect of dexmedetomidine post-treatment on the inflammatory response of astrocyte induced by lipopolysaccharide.

作者信息

Xie Cuiying, Wang Zhenhong, Tang Jiajia, Shi Zhiqian, He Zhenzhou

机构信息

Department of Anesthesiology and Surgical Intensive Care Unit, South Campus, Renji Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, 201112, China.

出版信息

Cell Biochem Biophys. 2015 Jan;71(1):407-12. doi: 10.1007/s12013-014-0213-0.

Abstract

To explore the effect of dexmedetomidine (DEX) post-treatment on the inflammatory response of astrocyte induced by lipopolysaccharide (LPS). The astrocytes of neonatal mice were primarily cultured in vitro. After purification and identification, the cells were divided into five groups: group C: control group; group L: astrocytes were treated with 1 μg/ml LPS for 24 h; group D1, D2, and D3: astrocytes were pretreated with 1 μg/ml for 24 h LPS, and then cultured with low (0.1 μM), medium (1 μM), high (10 μM) concentration of DEX for 30 min, respectively. The cell survival rate was detected by cell counting kit. The expressions of inducible nitric oxide synthase (iNOS) mRNA, tumor necrosis gactor-α (TNF-α) mRNA, and interleukin-1β (IL-1β) mRNA were measured by RT-PCR in cell lysis solution of every group. The concentration of nitric oxide (NO) was detected by Griess method. The concentrations of IL-1β and TNF-α were measured, respectively, by enzyme-linked immuno sorbent assay. Compared with the group C, the expressions of iNOS mRNA, TNF-α mRNA, and IL-1βm RNA were significantly up-regulated, the release of NO, TNF-α, and IL-1β was significantly increased in group L (P < 0.05). Compared with group L, mRNA levels of inflammation-related factors and release of inflammatory factors were significantly down-regulated in group D2 and D3 (P < 0.05). There was no statistical difference between group D1 and group L. Pre-treatment with medium and high concentration of DEX can inhibit the LPS-induced inflammatory response of astrocyte.

摘要

探讨右美托咪定(DEX)后处理对脂多糖(LPS)诱导的星形胶质细胞炎症反应的影响。新生小鼠星形胶质细胞进行体外原代培养。经纯化鉴定后,将细胞分为五组:C组:对照组;L组:星形胶质细胞用1μg/ml LPS处理24小时;D1、D2和D3组:星形胶质细胞先用1μg/ml LPS预处理24小时,然后分别用低(0.1μM)、中(1μM)、高(10μM)浓度的DEX培养30分钟。采用细胞计数试剂盒检测细胞存活率。采用RT-PCR法检测各组细胞裂解液中诱导型一氧化氮合酶(iNOS)mRNA、肿瘤坏死因子-α(TNF-α)mRNA和白细胞介素-1β(IL-1β)mRNA的表达。采用Griess法检测一氧化氮(NO)浓度。分别采用酶联免疫吸附测定法检测IL-1β和TNF-α浓度。与C组比较,L组iNOS mRNA、TNF-α mRNA和IL-1β mRNA表达明显上调,NO、TNF-α和IL-1β释放明显增加(P<0.05)。与L组比较,D2组和D3组炎症相关因子mRNA水平及炎症因子释放明显下调(P<0.05)。D1组与L组比较差异无统计学意义。中、高浓度DEX预处理可抑制LPS诱导的星形胶质细胞炎症反应。

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