Shufeng Jiedu capsules protect rats against LPS-induced acute lung injury via activating NRF2-associated antioxidant pathway

被引:7
|
作者
Liao, Qingwu [1 ]
Chen, Wenan [2 ]
Tong, Zhufeng [3 ]
Xue, Mingming [2 ]
Gu, Tianwen [2 ]
Yuan, Ying [4 ]
Song, Zhenju [2 ]
Tao, Zhengang [2 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Dept Anesthesia, Shanghai, Peoples R China
[2] Fudan Univ, Zhongshan Hosp, Emergency Dept, Shanghai, Peoples R China
[3] Wannan Med Coll, Dept Gen Practice, Yijishan Hosp, Wuhu, Anhui, Peoples R China
[4] Fudan Univ, Zhongshan Hosp, Geriatr Dept, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Shufeng Jiedu capsule (SFJDC); Acute lung injury; Antioxidant activity; NRF2; TRAUMATIC BRAIN-INJURY; PULMONARY INFLAMMATION; NRF2; FLAVONOIDS; UBIQUITINATION; INHIBITION; RESOLUTION;
D O I
10.14670/HH-18-293
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Shufeng Jiedu capsule (SFJDC) is a traditional Chinese medicine, which has been used for the treatment of respiratory infections for more than thirty years in Hunan (China). SFJDC protected rats against LPS-induced acute lung injury (ALI); however, the molecular mechanisms underlying the therapeutic effects of SFJDC remain unclear. Therefore, this study aimed at analyzing the major anti-inflammatory compounds of SFJDC and exploring the underlying molecular mechanisms. SFJDC dissolved in water was fingerprinted by UPLC/Q-TOF. Inflammation response was assessed by histopathological examination and ELISA assay. Arterial blood gases were also analyzed to evaluate the function of rat lungs. The expression levels of Kelch-like ECH-associating protein 1 (Keap1), Nrf2, heme oxygenase-1 (HO1), Cullin 3 (CUL3) and NQO1 were analyzed by Western blotting. Results indicated that SFJDC alleviated inflammation response by reducing the level of inflammatory cytokines, and upregulation of glutathione-S-transferase (GST) and superoxide dismutase (SOD) in lung tissues. Furthermore, SFJDC suppressed LPS-induced upregulation of Keap 1 and CUL3 in rat lungs. The expression of NRF2 HO1 and NQO1 were further upregulated by SFJDC in the presence of LPS, indicating that SFJDC might activate the NRF2-associated antioxidant pathway. In conclusion, SFJDC treatment may protect the rat lungs from LPS by alleviating the inflammation response via NRF2-associated antioxidant pathway.
引用
收藏
页码:317 / 324
页数:8
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