Dendropanax morbifera Branch Water Extract Increases the Immunostimulatory Activity of RAW264.7 Macrophages and Primary Mouse Splenocytes

• Published in: Journal of medicinal food Vol. 22; no. 11; p. 1136
• Main Authors: Song, Ji-Hye, Kwak, Sungmin, Kim, Hyunhee, Jun, Woojin, Lee, Jeongmin, Yoon, Ho-Geun, Kim, Yongjae, Choi, Kyung-Chul
• Format: Journal Article
• Language: English
• Published: United States 01.11.2019
• Subjects: Adjuvants, Immunologic - pharmacology; Animals; Araliaceae - chemistry; Cytokines - metabolism; Immunity, Innate; Macrophages - drug effects; Macrophages - immunology; Male; Mice; Mice, Inbred BALB C; NF-kappa B - metabolism; Nitric Oxide - metabolism; Nitric Oxide Synthase Type II - metabolism; Plant Bark - chemistry; Plant Extracts - pharmacology; Plant Leaves - chemistry; Polyacetylene Polymer - pharmacology; RAW 264.7 Cells; Signal Transduction; Spleen - cytology; Spleen - drug effects; Spleen - immunology; RAW264.7 cells; cytokines; immune stimulation; Dendropanax morbifera; NK activity
• ISSN: 1557-7600
• DOI: 10.1089/jmf.2019.4424

Polyacetylenes in the bark of trees have been reported to promote immune cell proliferation and to strengthen the innate immune system. The immunomodulatory potential of branch water extract (DBW) was evaluated by determining its effect on cell viability and the expression of cytokines and immune effector molecules in mouse RAW264.7 macrophages and splenocytes. Production of nitric oxide (NO), inducible nitric oxide synthase (iNOS), and cytokines (interleukin [IL]-1 , IL-2, and IFN- ) in RAW264.7 macrophages increased after treatment with DBW. The activation of components of the NF- B signaling pathway, including the phospho-I B and the expression and translocation of p65, a subunit of NF- B, were also increased in RAW264.7 mouse macrophage cells after treatment with DBW. In addition, when mice were orally administered DBW, splenocyte cytokines and NO production were increased in a dose-dependent manner relative to control-treated mice. Furthermore, natural killer cell activity in DBW-treated mice was determined by lactate dehydrogenase (LDH) release assay. LDH release also increased in response to DBW treatment. Taken together, these results indicate that extract enhances innate immunity by promoting NF- B signaling, leading to increased expression of proinflammatory cytokines and effector molecules. DBW therefore has potential therapeutic use in the context of immune stimulation.