Targeting TLR4 and regulating the Keap1/Nrf2 pathway with andrographolide to suppress inflammation and ferroptosis in LPS-induced acute lung injury

Yichen LI , Liting HUANG , Jilang LI , Siyuan LI , Jianzhen LV , Guoyue ZHONG , Ming GAO , Shilin YANG , Shan HAN , Wenhui HAO

Chinese Journal of Natural Medicines ›› 2024, Vol. 22 ›› Issue (10) : 914 -928.

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Chinese Journal of Natural Medicines ›› 2024, Vol. 22 ›› Issue (10) :914 -928. DOI: 10.1016/S1875-5364(24)60727-2
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Targeting TLR4 and regulating the Keap1/Nrf2 pathway with andrographolide to suppress inflammation and ferroptosis in LPS-induced acute lung injury

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Abstract

Acute lung injury (ALI) is a severe inflammatory condition with a high mortality rate, often precipitated by sepsis. The pathophysiology of ALI involves complex mechanisms, including inflammation, oxidative stress, and ferroptosis, a novel form of regulated cell death. This study explores the therapeutic potential of andrographolide (AG), a bioactive compound derived from Andrographis, in mitigating Lipopolysaccharide (LPS)-induced inflammation and ferroptosis. Our research employed in vitro experiments with RAW264.7 macrophage cells and in vivo studies using a murine model of LPS-induced ALI. The results indicate that AG significantly suppresses the production of pro-inflammatory cytokines and inhibits ferroptosis in LPS-stimulated RAW264.7 cells. In vivo, AG treatment markedly reduces lung edema, decreases inflammatory cell infiltration, and mitigates ferroptosis in lung tissues of LPS-induced ALI mice. These protective effects are mediated via the modulation of the Toll-like receptor 4 (TLR4)/Kelch-like ECH-associated protein 1(Keap1)/Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway. Molecular docking simulations identified the binding sites of AG on the TLR4 protein (Kd value: −33.5 kcal·mol−1), and these interactions were further corroborated by Cellular Thermal Shift Assay (CETSA) and SPR assays. Collectively, our findings demonstrate that AG exerts potent anti-inflammatory and anti-ferroptosis effects in LPS-induced ALI by targeting TLR4 and modulating the Keap1/Nrf2 pathway. This study underscores AG’s potential as a therapeutic agent for ALI and provides new insights into its underlying mechanisms of action.

Keywords

Andrographolide / Acute lung injury / Ferroptosis / Toll-like receptor 4 / Kelch-like ECH-associated protein 1/Nuclear factor erythroid 2-related factor 2

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Yichen LI, Liting HUANG, Jilang LI, Siyuan LI, Jianzhen LV, Guoyue ZHONG, Ming GAO, Shilin YANG, Shan HAN, Wenhui HAO. Targeting TLR4 and regulating the Keap1/Nrf2 pathway with andrographolide to suppress inflammation and ferroptosis in LPS-induced acute lung injury. Chinese Journal of Natural Medicines, 2024, 22(10): 914-928 DOI:10.1016/S1875-5364(24)60727-2

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Funding

China-ASEAN International Innovative Center for Health Industry of Traditional Chinese Medicine(AD20297142)

Guangxi Collaborative Innovation Center for Scientific Achievements Transformation and Applicationon Traditional Chinese Medicine(05020058)

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