Figure 5. Effects of AAIP on LPS-induced phosphorylation of ERK 1/2, JNK 1/2 and p38 MAP kinase in RAW264.7 cells. Cell were treated with vehicle or the indicated concentrations of AAIP (10-250 μM) for 1 h before incubation with LPS (100 ng/mL). Cell lysates were then prepared and subjected to Western blotting with antibodies specific for phosphorylated forms of ERK 1/2, JNK 1/2 and p38. Results represent three independent experiments (Qian et al. (2016))

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Inhibitory Effects and Molecular Mechanism of an Anti-inflammatory Peptide Isolated from Intestine of Abalone, Haliotis Discus Hannai on LPS-Induced Cytokine Production via the p-p38/p-JNK Pathways in RAW264.7 Macrophages

Zhong-Ji Qian, BoMi Ryu, Won Sun Park, IL-Whan Choi, Won-Kyo Jung

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