沙棘中1,5-二甲基柠檬酸对RAW 264.7小鼠巨噬细胞脂多糖诱导的炎症反应的抑制作用
Inhibitory Effect of 1,5-Dimethyl Citrate from Sea Buckthorn () on Lipopolysaccharide-Induced Inflammatory Response in RAW 264.7 Mouse Macrophages.
作者信息
Baek Su Cheol, Lee Dahae, Jo Mun Seok, Lee Kwang Ho, Lee Yong Hoon, Kang Ki Sung, Yamabe Noriko, Kim Ki Hyun
机构信息
School of Pharmacy, Sungkyunkwan University, Suwon 16419, Korea.
College of Korean Medicine, Gachon University, Seongnam 13120, Korea.
出版信息
Foods. 2020 Mar 2;9(3):269. doi: 10.3390/foods9030269.
L. (Elaeagnaceae; commonly known as "sea buckthorn" and "vitamin tree"), is a spiny deciduous shrub whose fruit is used in foods and traditional medicines. The fruit (berry) is rich in vitamin C, with a level exceeding that found in lemons and oranges. berries are usually washed and pressed to create pomace and juice. Today, the powder of the aqueous extract of berries are sold as a functional food in many countries. As part of our ongoing effort to identify bioactive constituents from natural resources, we aimed to isolate and identify those from the fruits of . Phytochemical analysis of the extract of fruits led to the isolation and identification of six compounds, namely, a citric acid derivative (), a phenolic (), flavonoids ( and ), and megastigmane compounds ( and ). Treatment with compounds - did not have any impact on the cell viability of RAW 264.7 mouse macrophages. However, pretreatment with these compounds suppressed lipopolysaccharide (LPS)-induced NO production in RAW 264.7 mouse macrophages in a concentration-dependent manner. Among the isolated compounds, compound was identified as the most active, with an IC of 39.76 ± 0.16 μM. This value was comparable to that of the -methyl-L-arginine acetate salt, a nitric oxide synthase inhibitor with an IC of 28.48 ± 0.05 μM. Western blot analysis demonstrated that compound inhibited the LPS-induced expression of IKKα/β (IκB kinase alpha/beta), I-κBα (inhibitor of kappa B alpha), nuclear factor kappa-B (NF-κB) p65, iNOS (inducible nitric oxide synthase), and COX-2 (cyclooxygenase-2) in RAW 264.7 cells. Furthermore, LPS-stimulated cytokine production was detected using a sandwich enzyme-linked immunosorbent assay. Compound decreased interleukin 6 (IL-6) and tumor necrosis factor alpha (TNF-α) production in LPS-stimulated RAW 264.7 cells. In summary, the mechanism of action of included the suppression of LPS-induced NO production in RAW 264.7 cells by inhibiting IKKα/β, I-κBα, NF-κB p65, iNOS, and COX-2, and the activities of IL-6 and TNF-α.
沙棘属(胡颓子科;通常被称为“沙棘”和“维生素树”)是一种多刺落叶灌木,其果实被用于食品和传统药物中。果实(浆果)富含维生素C,含量超过柠檬和橙子。浆果通常经过清洗和压榨以制成果渣和果汁。如今,沙棘浆果水提取物粉末在许多国家作为功能性食品出售。作为我们从自然资源中鉴定生物活性成分的持续努力的一部分,我们旨在从沙棘果实中分离和鉴定这些成分。对沙棘果实提取物的植物化学分析导致分离和鉴定出六种化合物,即一种柠檬酸衍生物()、一种酚类()、黄酮类化合物(和)以及大柱香波龙化合物(和)。用化合物 - 处理对RAW 264.7小鼠巨噬细胞的细胞活力没有任何影响。然而,用这些化合物预处理以浓度依赖的方式抑制了RAW 264.7小鼠巨噬细胞中脂多糖(LPS)诱导的NO产生。在分离出的化合物中,化合物被鉴定为最具活性,IC50为39.76±0.16μM。该值与 - 甲基 - L - 精氨酸乙酸盐相当,后者是一种一氧化氮合酶抑制剂,IC50为28.48±0.05μM。蛋白质印迹分析表明,化合物抑制了RAW 264.7细胞中LPS诱导的IKKα/β(IκB激酶α/β)、I - κBα(κB抑制因子α)、核因子κB(NF - κB)p65、诱导型一氧化氮合酶(iNOS)和环氧化酶 - 2(COX - 2)的表达。此外,使用夹心酶联免疫吸附测定法检测LPS刺激的细胞因子产生。化合物降低了LPS刺激的RAW 264.7细胞中白细胞介素6(IL - 6)和肿瘤坏死因子α(TNF - α)的产生。总之,沙棘的作用机制包括通过抑制IKKα/β、I - κBα、NF - κB p65、iNOS和COX - 2以及IL - 6和TNF - α的活性来抑制RAW 264.7细胞中LPS诱导的NO产生。