Jiwu Wang1,
Fei Xiao2,
Shanwu Dong3,
Yongli Chen3,
Xiaozhen Chen3
1Department of Cardiothoracic Surgery, Wuhan Fourth Hospital, Wuhan 430030, Hubei Province, China;
2Department of Abdominal Surgery, Wuhan Fourth Hospital, Wuhan 430030, Hubei Province, China;
3Department of Pediatrics, Wuhan Fourth Hospital, Wuhan 430030, Hubei Province, China.
For correspondence:- Xiaozhen Chen
Email: shixingtang4945762@163.com
Accepted: 3 May 2023
Published: 30 May 2023
Citation:
Wang J, Xiao F, Dong S, Chen Y, Chen X.
Protective effect of baicalin against lipopolysaccharide-induced acute lung injury in rats, and the mechanism of action. Trop J Pharm Res 2023; 22(5):1031-1036
doi:
10.4314/tjpr.v22i5.14
© 2023 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 study the protective influence of baicalin (BA) against LPS-mediated acute lung injury (ALI) in a rat model.
Methods: Twenty-seven Sprague-Dawley (SD) rats were assigned (9 rats each) to groups as follows: normal control (NC) treated intraperitoneally with normal saline; lipopolysaccharide (LPS) group treated with 10 mg/kg LPS; and lipopolysaccharide and baicalin (LPS + Ba) group treated with 100 mg/kg LPS, followed 15 min later by 10 mg/kg of baicalin. Pathological changes were assessed by H & E staining. Different types of cells were identified and counted using Rayleigh Giemsa staining. Levels of IL-6 and TNF-α and IL-1β in pulmonary tissue were determined by enzyme-linked immunosorbent assay (ELISA). Matute-Bello scoring method was applied to evaluate the extent of lung injury, while pulmonary expression levels of Nrf2, HO-1 and NQO1 were assayed with Western blot.
Results: Lung injury score, and numbers of neutrophils and macrophages were significantly higher in LPS than in NC group. Inflammatory score, and numbers of neutrophils and macrophages in LPS + BA group were significantly lower than those in LPS group (p < 0.05). Compared with NC group, lung tissue levels of IL-6, TNF-α and IL-1β in LPS group were significantly increased, but were significantly reduced in LPS + BA rats, relative to LPS rats (p < 0.05). expression levels of Nrf2, HO-1 and NQO1 in lung tissue were significantly lower in LPS group than in NC group (p < 0.05) but higher in lung tissue of LPS + BA group, relative to LPS group.
Conclusion: Baicalin (BA) protects rats from LPS-induced ALI by enhancing the expressions of Nrf2 and HO-1 through activation of Nrf2/ARE signal pathway. These findings may be useful in developing novel BA-based anti-inflammatory drugs
Keywords: Baicalin, Acute lung injury, Nrf2/ARE, Matute-Bello score, Neutrophils, Macrophages, Inflammatory score