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SL significantly inhibited the intrahepatic synthesis of several disease-related pro-inflammatory cytokine mRNAs, i.e., for TNF, interferon-gamma (IFN-g), IL-4, and IL-2, intrahepatic induction of iNOS, and intrahepatic activation of NF-B (Morishima et al., 2010

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These actions facilitate cell migration and organization at the site of injury, supporting tissue regeneration and structural recovery