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Neohesperidin dihydrochalcone down-regulates MyD88-dependent and -independent signaling by inhibiting endotoxin-induced trafficking of TLR4 to lipid rafts
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文摘

NHDC attenuates d-GalN/LPS-induced fulminant hepatic failure.

NHDC inhibits LPS-induced myeloid differentiation factor 88 dependent signaling.

NHDC inhibits LPS-induced TIR-containing adapter molecule dependent signaling.

NHDC inhibits LPS-induced the translocation of TLR4 into lipid raft domains.

These results implied a new application of NHDC as a hepatoprotective agent.

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