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Original Research Article | OPEN ACCESS

Regulation of RhoA/ROCK1 signaling pathway by miR-26b in sepsis-induced acute lung injury

Yi Mao1, Yi Gao2, Zhiwei Zhao1, Jinbo Zhang1, Meiping Dong1, Liexiang Cao1

1Emergency Center, The First People's Hospital of Wenling, Wenling, Zhejiang 317500, China; 2Department of Anesthesiology, The First People's Hospital of Wenling, Wenling, Zhejiang 317500, China.

For correspondence:-  Liexiang Cao   Email: aornrutai.p@pnu.ac.th   Tel:+8613758672656

Accepted: 18 July 2022        Published: 28 August 2022

Citation: Mao Y, Gao Y, Zhao Z, Zhang J, Dong M, Cao L. Regulation of RhoA/ROCK1 signaling pathway by miR-26b in sepsis-induced acute lung injury. Trop J Pharm Res 2022; 21(8):1633-1638 doi: 10.4314/tjpr.v21i8.8

© 2022 The authors.
This is an Open Access article that uses a funding model which does not charge readers or their institutions for access and distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0) and the Budapest Open Access Initiative (http://www.budapestopenaccessinitiative.org/read), which permit unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited..

Abstract

Purpose: To investigate the role of miR-26b in the regulation of RhoA/ ROCK1 signaling pathway in acute lung injury (ALI) caused by sepsis.
Methods: Thirty male rats were randomized into sham group (SG), cecal ligation and puncture (CLP) group (CG) and miR-26b mimic group (MG). Hematoxylin and eosin (H & E) staining assay was performed to determine the pathological characteristics of rat lung tissues in each group, while enzyme-linked immunosorbent assay (ELISA) was conducted to determine TNF-α and IL-1β levels. The miR-26b expression was evaluated by quantitative reverse transcription polymerase chain reaction (qRT-PCR), while RhoA and Rock1 protein levels were assessed using western blotting.
Results: The CG had significant lung injury in comparison with the SG. There were significant elevation in TNF-α and IL-1β levels (p < 0.05). RhoA and ROCK1 levels in lung tissue were noticeably elevated in CG (p < 0.05). After treatment, lung injury in MG was reduced in contrast to CG. The MG showed statistically significant decrease (p < 0.05) in the levels of TNF-α and IL-1β, while the lung tissue mRNA expression and the RhoA and ROCK1 expression levels were significantly reduced in MG (p < 0.05).
Conclusion: The MiR-26b mimics plays an important role in the treatment of ALI induced by sepsis in rats by regulating RhoA/ROCK1 signaling pathway. Thus, the findings of this study provide a theoretical basis for clinical studies on the use of miR-26b in the therapy of sepsis.

Keywords: miR-26b, RhoA/ROCK1, Sepsis, Acute lung injury

Impact Factor
Thompson Reuters (ISI): 0.523 (2021)
H-5 index (Google Scholar): 39 (2021)

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