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使用SG - 030和来自YRK005的低聚葡萄糖的合生元的免疫刺激活性。

Immunostimulatory Activity of Synbiotics Using SG-030 and Glucooligosaccharides from YRK005.

作者信息

Kwon Ayeon, Park Young-Seo

机构信息

Department of Food Science and Biotechnology, Gachon University, Seongnam-si 13120, Korea.

出版信息

Microorganisms. 2021 Nov 25;9(12):2437. doi: 10.3390/microorganisms9122437.

Abstract

Much attention has been recently paid to the health benefits of synbiotics, a combination of probiotics and prebiotics. In this study, synbiotics were prepared by combining lactic acid bacteria with potential as probiotics and purified glucooligosaccharides, and their immunostimulatory activity was evaluated using RAW 264.7 macrophage cells. A lactic acid bacteria strain with high antioxidant activity, acid and bile salt tolerance, adhesion to Caco-2 cells, and nitric oxide (NO) production was selected as a potential probiotic strain. The selected strain, isolated from forsythia, was identified as SG-030. The purified glucooligosaccharides produced from YRK005 were used as prebiotics. RAW 264.7 cells were treated with synbiotics in two ways. One way was a simultaneous treatment with lactic acid bacteria and glucooligosaccharides. The other way was to pre-culture the lactic acid bacteria with glucooligosaccharides followed by treatment with synbiotic culture broth or synbiotic culture supernatant. In both cases, synbiotics synergistically increased NO production in RAW 264.7 cells. In addition, synbiotics treatment increased the expression of tissue necrosis factor-α, interleukin (IL)-1β, IL-6, and inducible nitric oxide synthase genes. Synbiotics also increased the expression of P38, extracellular signal-regulated kinases, c-Jun -terminal kinases, phosphoinositide 3-kinase, and Akt proteins. The results confirmed that the synbiotics prepared in this study exhibited synergistic immunostimulatory activity.

摘要

近年来,合生元(益生菌和益生元的组合)对健康的益处备受关注。在本研究中,通过将具有益生菌潜力的乳酸菌与纯化的低聚葡萄糖组合制备合生元,并使用RAW 264.7巨噬细胞评估其免疫刺激活性。选择了一种具有高抗氧化活性、耐酸和耐胆盐、能黏附于Caco-2细胞且能产生一氧化氮(NO)的乳酸菌菌株作为潜在的益生菌菌株。从连翘中分离出的所选菌株被鉴定为SG-030。将YRK005产生的纯化低聚葡萄糖用作益生元。RAW 264.7细胞用两种方式进行合生元处理。一种方式是同时用乳酸菌和低聚葡萄糖处理。另一种方式是先用低聚葡萄糖预培养乳酸菌,然后用合生元培养液或合生元培养上清液处理。在这两种情况下,合生元均协同增加RAW 264.7细胞中NO的产生。此外,合生元处理增加了肿瘤坏死因子-α、白细胞介素(IL)-1β、IL-6和诱导型一氧化氮合酶基因的表达。合生元还增加了P38、细胞外信号调节激酶、c-Jun末端激酶、磷酸肌醇3激酶和Akt蛋白的表达。结果证实,本研究中制备的合生元具有协同免疫刺激活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4813/8703668/6275a8fc67fc/microorganisms-09-02437-g001.jpg

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