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학술논문

Salidroside attenuates sepsis-induced acute lung injury by inhibiting ferroptosis-dependent pathway

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영문명
발행기관
대한생리학회-대한약리학회
저자명
Lingling Zhen Mingtong Hou Shengbao Wang
간행물 정보
『The Korean Journal of Physiology & Pharmacology』제28권 제6호, 549~558쪽, 전체 10쪽
주제분류
의약학 > 의학일반
파일형태
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발행일자
2024.11.01
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국문 초록

Sepsis triggers a systemic inflammatory response that can lead to acute lung injury (ALI). Salidroside (SAL) has many pharmacological activities such as antiinflammatory and anti-oxidation. The objective of the study was to explore the mechanism of SAL on ALI caused by sepsis. A model of ALI in septic mice was established by cecal ligation and puncture. Following SAL treatment, the effect of SAL on the ferroptosis pathway in mice was analyzed. The pathological damage of lung tissue, the levels of inflammatory factors and apoptosis in bronchoalveolar lavage fluid (BALF) of mice were evaluated, and the changes of gene expression level and metabolite content abundance were explored by combining transcriptomics and metabolomics analysis. The effect of SAL on ferroptosis in mice with lung injury was observed by intraperitoneal injection of ferroptosis activator Erastin or ferroptosis inhibitor Ferrostatin-1 to promote or inhibit ferroptosis in mice. SAL significantly alleviated the pathological damage of lung tissue, decreased the number of TUNEL positive cells and the levels of TNF-α, IL-1β, IL-6 in BALF, and increased the level of IL- 10 in lung injury mice. Moreover, the Fe2+ content and malondialdehyde decreased significantly, the reactive oxygen species and glutathione content increased significantly, and the arachidonic acid metabolites 20-hydroxyeicosatetraenoic acid (20- HETE), (5Z, 8Z, 10E, 14Z)-12-Oxoeicosa-5,8,10,14-tetraenoic acid (12-OxOETE), (5Z, 8Z, 10E, 14Z)-(12S)-12-Hydroxyeicosa-5,8,10,14-tetraenoic acid (12(S)-HETE), (5Z, 8Z, 14Z)-11,12-Dihydroxyeicosa-5,8,14-trienoic acid (11,12-DHET), (5Z, 11Z, 14Z)-8,9- Dihydroxyeicosa-5,11,14-trienoic acid, Leukotriene B4, Leukotriene D4 were significantly up-regulated after SAL treatment. Salidroside alleviates ALI caused by sepsis by inhibiting ferroptosis.

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APA

Lingling Zhen,Mingtong Hou,Shengbao Wang. (2024).Salidroside attenuates sepsis-induced acute lung injury by inhibiting ferroptosis-dependent pathway. The Korean Journal of Physiology & Pharmacology, 28 (6), 549-558

MLA

Lingling Zhen,Mingtong Hou,Shengbao Wang. "Salidroside attenuates sepsis-induced acute lung injury by inhibiting ferroptosis-dependent pathway." The Korean Journal of Physiology & Pharmacology, 28.6(2024): 549-558

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