Kim Hui-Seong, Kwon Ok-Kyoung, Park Ji-Won, Jeong Hye Gwang, Oh Sei-Ryang, Lee Hyeong-Kyu, Bach Tran The, Hai Do Van, Ahn Kyung-Seop
Biomolecular Science, University of Science and Technology.
Biosci Biotechnol Biochem. 2013;77(12):2356-61. doi: 10.1271/bbb.130429. Epub 2013 Dec 7.
The biological activity of Mastixia arborea (MA) relates to inflammation, but the underlying mechanisms are largely unknown. We confirmed the anti-inflammatory effects of a methanol extract of MA extract on lipopolysaccharide (LPS)-stimulated RAW264.7 mouse macrophage cells and carrageenan-induced mice paw edema. The MA extract significantly inhibited nitric oxide (NO), prostaglandin E2 (PGE2), interleukin-1β (IL-1β), and IL-6 production in LPS-stimulated RAW264.7 cells. In vitro expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) was suppressed by the extract. The extract attenuated acute inflammatory responses in carrageenan-induced mice paw edema. A mechanism study indicated that translocation of the NF-κB (p65) subunit into the nucleus and phosphorylation of ERK and JNK were inhibited by the extract. These results indicate that the extract is an effective suppressor of the inflammatory response, blocking the phosphorylation of ERK and JNK and the translocation of NF-κB in macrophages, thereby producing an anti-inflammatory effect in vivo.
多花轮钟草的生物活性与炎症有关,但其潜在机制尚不清楚。我们证实了多花轮钟草甲醇提取物对脂多糖(LPS)刺激的RAW264.7小鼠巨噬细胞和角叉菜胶诱导的小鼠足爪水肿具有抗炎作用。多花轮钟草提取物显著抑制LPS刺激的RAW264.7细胞中一氧化氮(NO)、前列腺素E2(PGE2)、白细胞介素-1β(IL-1β)和IL-6的产生。提取物抑制了诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的体外表达。该提取物减轻了角叉菜胶诱导的小鼠足爪水肿中的急性炎症反应。机制研究表明,提取物抑制了NF-κB(p65)亚基向细胞核的转位以及ERK和JNK的磷酸化。这些结果表明,该提取物是炎症反应的有效抑制剂,可阻断巨噬细胞中ERK和JNK的磷酸化以及NF-κB的转位,从而在体内产生抗炎作用。