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Effects of compounds isolated from a Litsea japonica fruit extract on the TNF-α signaling pathway and cell viability

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Abstract

Tumor necrosis factor-α (TNF-α) plays an important role in inflammatory responses. Deregulated activation of TNF-α signaling is associated with various inflammatory diseases. In view of the finding that the seventy percent ethanol extract of Litsea japonica (LJE) interferes with TNF-α-induced NF-κB activation, activity- guided fractionation was performed to identify the active components of the extract. The EtOAc, CH2Cl2 and n-Hexane fractions of LJE induced suppression of inhibitor of κB (IκB) kinase (IKK), p38 mitogen-activated protein kinase (MAPK) and c-Jun N-terminal kinase (JNK), and significant reduction of TNF-α- induced NF-κB activation. From the CH2Cl2 fraction, hamabiwalactone A, hamabiwalactone B, litsenolide B2 and litsenolide C2 were identified to inhibit TNF- α-induced NF-κB activation. The cytotoxic activities of these lactone compounds were additionally evaluated.

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Correspondence to Yoon-Jae Song.

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Won, J., Kim, JE., Choi, D.H. et al. Effects of compounds isolated from a Litsea japonica fruit extract on the TNF-α signaling pathway and cell viability. Mol. Cell. Toxicol. 12, 37–44 (2016). https://doi.org/10.1007/s13273-016-0006-1

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  • DOI: https://doi.org/10.1007/s13273-016-0006-1

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