Literature DB >> 32594289

miR-128-3p enhances the protective effect of dexmedetomidine on acute lung injury in septic mice by targeted inhibition of MAPK14.

Li Ding1, Xiang Gao2, Shenghui Yu2, Liufang Sheng3.   

Abstract

To investigate the role of miR-128-3p and MAPK14 in the dexmedetomidine treatment of acute lung injury in septic mice. SPF C57BL/6 mice were divided into 8 groups. The pathological changes and wet/dry weight ratio (W/D), PaO2, PaCO2, MDA, SOD and MPO levels in lung tissue and the serum levels of inflammation factors were observed. Dual luciferase reporter assay was used to detect the targeting relationship of miR-128-3p and MAPK14, and qPCR and WB were used to detect the expression of miR-128-3p and MAPK14. Compared with the Normal group, other groups had lower MDA, MPO, inflammatory factors levels and the expression level of MAPK14, while the content of SOD and the expression level of miR-128-3p was significantly decreased (all p < 0.05). Compared with the Model group, the contents of MDA, MPO, inflammatory factors in the DEX group and miR-128-3p mimic group were significantly decreased, and the content SOD was significantly increased, however, opposite results were occurred in oe-MAPK14 group (all p < 0.05). Compared with the DEX group, all the indicators in miR-128-3p mimic+DEX group showed significant improvement (all p < 0.05). Compared with the miR-128-3p mimic group, all the indicators were deteriorated in the miR-128-3p mimic+oe-MAPK14 group (all p < 0.05). The combination of DEX and oe-MAPK14 blocked the protective effect of dexmedetomidine on acute lung injury in septic mice. miR-128-3p can further enhance the protective effect of dexmedetomidine on acute lung injury in septic mice by targeting and inhibiting MAPK14 expression.

Entities:  

Keywords:  Acute lung injury; Dexmedetomidine; MAPK14; Sepsis; miR-128-3p

Mesh:

Substances:

Year:  2020        PMID: 32594289     DOI: 10.1007/s10863-020-09842-8

Source DB:  PubMed          Journal:  J Bioenerg Biomembr        ISSN: 0145-479X            Impact factor:   2.945


  5 in total

1.  Diagnostic and Predictive Values of Ferroptosis-Related Genes in Child Sepsis.

Authors:  Zhi Li; Chi Zhang; Yiqi Liu; Fang Wang; Baoling Zhao; Junmei Yang; Yongjing Zhao; Hong Zhao; Guiqiang Wang
Journal:  Front Immunol       Date:  2022-06-30       Impact factor: 8.786

2.  Long non-coding RNA NEAT1 promotes lipopolysaccharide-induced acute lung injury by regulating miR-424-5p/MAPK14 axis.

Authors:  Rui Zhang; Lina Chen; Fei Huang; Xiaorong Wang; Cuihong Li
Journal:  Genes Genomics       Date:  2021-04-26       Impact factor: 1.839

3.  Identification of the TF-miRNA-mRNA co-regulatory networks involved in sepsis.

Authors:  Xiaoqian Luo; Weina Lu; Jianfeng Zhao; Jun Hu; Enjiang Chen; Shi Fu; Qinghui Fu
Journal:  Funct Integr Genomics       Date:  2022-03-24       Impact factor: 3.674

4.  Atractylenolide III alleviates sepsis-mediated lung injury via inhibition of FoxO1 and VNN1 protein.

Authors:  Ji-Ding Fu; Chun-Hui Gao; Shi-Wei Li; Yan Tian; Shi-Cheng Li; Yi-Er Wei; Le-Wu Xian
Journal:  Acta Cir Bras       Date:  2021-10-08       Impact factor: 1.388

5.  LncRNA XIST knockdown alleviates LPS-induced acute lung injury by inactivation of XIST/miR-132-3p/MAPK14 pathway : XIST promotes ALI via miR-132-3p/MAPK14 axis.

Authors:  Chen Li; Jian-Hua Liu; Jing Su; Wei-Jia Lin; Jian-Qing Zhao; Zhi-Hua Zhang; Qi Wu
Journal:  Mol Cell Biochem       Date:  2021-08-03       Impact factor: 3.396

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.