Department of Companion and Laboratory Animal Science, Kongju National University, Yesan, Chungcheongnam 32439, Republic of Korea.
MBG Group, Daejeon 35240, Republic of Korea.
Mol Med Rep. 2019 Mar;19(3):2087-2096. doi: 10.3892/mmr.2019.9887. Epub 2019 Jan 22.
Dendropanax morbifera (D. morbifera), known as Dendro, means 'omnipotent drug' (Panax), and has been called the panacea tree. Various studies on D. morbifera are currently ongoing, aiming to determine its medicinal uses. The present study investigated the anti‑inflammatory effects and underlying mechanism of a natural extract of D. morbifera leaves (DPL) in lipopolysaccharide (LPS)‑stimulated RAW264.7 macrophages. In the present study, the following assays and models were used: MTT assay, nitric oxide (NO) assay, western blotting, ELISA and mouse models of atopic dermatitis. DPL extract markedly reduced the production of NO, inducible NO synthase and interleukin‑6, as well as the nuclear translocation of nuclear factor‑κB (NF‑κB). Additionally, the LPS‑induced activation of extracellular signal‑regulated kinase 1/2 (ERK1/2), P38 and c‑Jun N‑terminal kinase (JNK) was suppressed by DPL extract. Taken together, these results indicate that NF‑κB, ERK1/2, P38 and JNK may be potential molecular targets of DPL extract in the LPS‑induced inflammatory response. Subsequently, the present study investigated the effects of DPL extract in a 2,4‑dinitrochlorobenzene‑induced atopic dermatitis mouse model. Ear thickness, serum immunoglobulin E levels and histological analysis revealed that the DPL extract was effective in attenuating the inflammatory response. These results indicate that DPL extract has anti‑inflammatory potential and may be developed as a botanical drug to treat atopic dermatitis.
美藤果(Dendropanax morbifera),又名全能药(Panax),被称为万灵药树。目前正在进行各种关于美藤果的研究,旨在确定其药用用途。本研究调查了美藤果叶天然提取物(DPL)在脂多糖(LPS)刺激的 RAW264.7 巨噬细胞中的抗炎作用及其潜在机制。在本研究中,使用了以下测定和模型:MTT 测定、一氧化氮(NO)测定、western blot、ELISA 和过敏性皮炎小鼠模型。DPL 提取物显著降低了 NO、诱导型一氧化氮合酶和白细胞介素-6 的产生,以及核因子-κB(NF-κB)的核易位。此外,DPL 提取物抑制了 LPS 诱导的细胞外信号调节激酶 1/2(ERK1/2)、p38 和 c-Jun N-末端激酶(JNK)的激活。综上所述,这些结果表明 NF-κB、ERK1/2、p38 和 JNK 可能是 DPL 提取物在 LPS 诱导的炎症反应中的潜在分子靶标。随后,本研究在 2,4-二硝基氯苯诱导的过敏性皮炎小鼠模型中研究了 DPL 提取物的作用。耳厚度、血清免疫球蛋白 E 水平和组织学分析表明,DPL 提取物可有效减轻炎症反应。这些结果表明 DPL 提取物具有抗炎潜力,可开发为治疗过敏性皮炎的植物药。