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• W4225845150 abstract "To investigate the therapeutic effect of Buyang huanwu decoction (BYHWD) on sepsis-induced myocardial injury (SIMI) and explore the mechanism by which BYHWD mitigates SIMI.The Lipopolysaccharide (LPS)-induced SIMI mouse model was established to detect the effect of BYHWD-low (1 mg/kg), BYHWD-middle (5 mg/kg), and BYWHD-high (20 mg/kg) on SIMI. The survival of these BYHWD-treated septic mice was investigated. The histology of myocardial tissues was determined by hematoxylin and eosin (H&E) staining. The apoptotic index and inflamed microenvironment of myocardial tissues were assessed by immunofluorescent staining (IF) and flow cytometry analysis. Liquid chromatography-mass spectrometry (LC-MS/MS) was employed to determine the key chemical components in the serum of BYHWD-loaded septic mice. Immunoblotting assay was utilized to detect NF-κB and TGF-β signaling activity, and M1/M2-macrophage markers using RAW264.7 cells.The high dosage of BYHWD (BYHWD-high, 20 mg/Kg) significantly attenuated SIMI and improved the survival of septic mice. The BYHWD-high solution markedly reduced myocardial cell apoptosis and mitigated the inflamed microenvironment by suppressing CD45+ immune cell infiltration. Importantly, BYHWD decreased macrophage accumulation and promoted an M2-macrophage polarization. Paeoniflorin (PF) and calycosin-7-O-β-glucoside (CBG) were identified as the key molecules in BYWHD with therapeutic effect. PF (10 μM) and CBG (1 μM) inhibited NF-κB signaling, meanwhile they upregulated the TGF-β pathway, thereby facilitating an M2-macrophage phenotypic transition in RAW264.7 cells.BYHWD, with two effective components PF and CBG, can mitigate SIMI by suppressing the inflamed myocardial microenvironment and skewing an immunosuppressive M2-macrophage phenotype." @default.
• W4225845150 created "2022-05-05" @default.
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• W4225845150 date "2022-01-01" @default.
• W4225845150 modified "2023-09-28" @default.
• W4225845150 title "Buyang Huanwu Decoction (BYHWD) Alleviates Sepsis Induced Myocardial Injury by Suppressing Local Immune Cell Infiltration and Skewing M2 Macrophage Polarization" @default.
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• W4225845150 doi "https://doi.org/10.2139/ssrn.4049555" @default.
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