黑蒜提取物对脂多糖诱导RAW264.7细胞炎症因子的影响  被引量:12

The effect of aged black garlic extract on cytokines in LPS-stimulated RAW 264.7 cells

在线阅读下载全文

作  者:罗海青[1,2,3] 吴磊[2] 强倩[1,2] 朱翠玲[1,2,3] 沈婷[1,2] 王新风[1,2] 纪丽莲[1,2,3] 胡卫成[1,2] 

机构地区:[1]淮阴师范学院,江苏省高校区域现代农业与环境保护协同创新中心,淮安223300 [2]淮阴师范学院生命科学学院,江苏省环洪泽湖生态农业生物技术重点实验室,淮安223300 [3]扬州大学食品科学与工程学院,扬州225127

出  处:《食品科技》2017年第8期199-205,共7页Food Science and Technology

基  金:江苏省自然科学基金项目(BK20150414)

摘  要:目的:以黑蒜提取物为研究对象,探讨其对脂多糖(LPS)刺激RAW264.7细胞的体外抗炎作用及其机制。方法:采用噻唑蓝(MTT)法检测不同浓度的黑蒜提取物对RAW264.7细胞活性的影响;采用Griess法检测黑蒜提取物对LPS刺激RAW264.7细胞的一氧化氮(NO)释放量;采用酶联免疫吸附法(ELISA)检测细胞上清液中PGE2、IL-1β及IL-6的分泌量;采用反转录PCR(RT-PCR)和免疫印迹法(Western blot)检测COX-2、i NOS m RNA及蛋白的表达。结果:黑蒜提取物能明显抑制LPS诱导的RAW264.7巨噬细胞NO、PGE2、IL-1β和IL-6的分泌,不同程度从转录和翻译水平抑制COX-2和i NOS的表达。结论:初步证实了黑蒜具有抗炎作用,其作用与在转录水平和翻译水平上抑制i NOS和COX-2有关。Objective: This study was aimed to investigate the anti-inflammatory effect of aged black garlic extract on lipopolysaccharide (LPS)-stimulated RAW 264.7 cells and its potential mechanism. Method: Cell viability was determined by MTT assay, the production of nitric oxide (NO) production was evaluated by Griess reagent assay. The production of prostaglandin E2 (PGE2), interleukin-6 (IL-6), and interleukin-1β (IL-1) were determined by immunosorbent assay (ELISA). The expression of inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) were investigated by the reverse transeriptase- polymerase chain reaction (RT-PCR) and Western blot. Results: Black garlic extract significantly inhibited the LPS-induced production of NO, PGE2, IL-6, and IL-1β. It also effectively attenuated iNOS and COX- 2 mRNA and protein expression. Conclusion: Overall, our data suggest that aged black garlic possess significant anti-inflammatory properties by down-regulation of iNOS and COX-2 expression from transcriptional and translational levels.

关 键 词:黑蒜 巨噬细胞 细胞因子 抗炎 

分 类 号:R284.2[医药卫生—中药学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象