Protective mechanism of quercetin in alleviating sepsis-related acute respiratory distress syndrome based on network pharmacology and in vitro experiments

BACKGROUND:Sepsis-related acute respiratory distress syndrome(ARDS)has a high mortality rate,and no effective treatment is available currently.Quercetin is a natural plant product with many pharmacological activities,such as antioxidative,anti-apoptotic,and anti-inflammatory effects.This study aimed to elucidate the protective mechanism of quercetin against sepsis-related ARDS.METHODS:In this study,network pharmacology and in vitro experiments were used to investigate the underlying mechanisms of quercetin against sepsis-related ARDS.Core targets and signaling pathways of quercetin against sepsis-related ARDS were screened and were verified by in vitro experiments.RESULTS:A total of 4,230 targets of quercetin,360 disease targets of sepsis-related ARDS,and 211 intersection targets were obtained via database screening.Among the 211 intersection targets,interleukin-6(IL-6),tumor necrosis factor(TNF),albumin(ALB),AKT serine/threonine kinase 1(AKT1),and interleukin-1β(IL-1β)were identified as the core targets.A Gene Ontology(GO)enrichment analysis revealed 894 genes involved in the inflammatory response,apoptosis regulation,and response to hypoxia.Kyoto Encyclopedia of Genes and Genomes(KEGG)enrichment analysis identified 106 pathways.After eliminating and generalizing,the hypoxia-inducible factor-1(HIF-1),TNF,nuclear factor-κB(NF-κB),and nucleotide-binding and oligomerization domain(NOD)-like receptor signaling pathways were identified.Molecular docking revealed that quercetin had good binding activity with the core targets.Moreover,quercetin blocked the HIF-1,TNF,NF-κB,and NODlike receptor signaling pathways in lipopolysaccharide(LPS)-induced murine alveolar macrophage(MH-S)cells.It also suppressed the inflammatory response,oxidative reactions,and cell apoptosis.CONCLUSION:Quercetin ameliorates sepsis-related ARDS by binding to its core targets and blocking the HIF-1,TNF,NF-κB,and NOD-like receptor signaling pathways to reduce inflammation,cell apoptosis,and oxidative stress.

Review of all-inorganic perovskites and their tandem solar cells with crystalline silicon

In widely studied organic-inorganic hybrid perovskites,the organic component tends to volatilize and decompose under high temperatures,oxygen,and humidity,which adversely affects the performance and longevity of the associated solar cells.In contrast,all-inorganic perovskites demonstrate superior stability under these conditions and offer photoelectric properties comparable to those of their hybrid counterparts.The potential of tandem solar cells(TSCs)made from all-inorganic perovskites is especially promising.This review is the first to address recent advancements in TSCs that use all-inorganic perovskites and crystalline silicon(c-Si),both domestically and internationally.This work provides a systematic and thorough analysis of the current challenges faced by these systems and proposes rational solutions.Additionally,we elucidate the regulatory mechanisms of all-inorganic perovskites and their TSCs when combined with c-Si,summarizing the corresponding patterns.Finally,we outline future research directions for all-inorganic perovskites and their TSCs with c-Si.This work offers valuable insights and references for the continued advancement of perovskitebased TSCs.