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GG条件培养基调节J774小鼠巨噬细胞中的急性活性氧和一氧化氮。

GG conditioned media modulates acute reactive oxygen species and nitric oxide in J774 murine macrophages.

作者信息

Seenappanahalli Nanjundaiah Yashaswini, Wright David A, Baydoun Anwar R, O'Hare William T, Ali Zulfiqur, Khaled Zahangir, Sarker Mosharraf H

机构信息

School of Science and Engineering, Teesside University, TS1 3BA, UK.

School of Life and Medical Sciences, University of Hertfordshire, AL 10 9AB, UK.

出版信息

Biochem Biophys Rep. 2016 Mar 7;6:68-75. doi: 10.1016/j.bbrep.2016.03.003. eCollection 2016 Jul.

Abstract

Phagocytes such as macrophages are capable of detecting and killing pathogenic bacteria by producing reactive oxygen and nitrogen species. Formation of free radicals in macrophages may be regulated by probiotics or by factors released by probiotics but yet to be identified. Thus, studies were carried out to determine whether cell-free conditioned medium obtained from cultures of GG (LGG-CM) regulate production of reactive oxygen species (ROS) and/or nitric oxide (NO) in macrophages. J774 macrophages in culture were loaded with either HDCFDA for monitoring ROS or with DAFFM-DA for NO detection. Free radical production was measured on a fluorescence microplate reader and changes were analysed by Cumulative sum (CuSum) calculations. Low concentration of LGG-CM (10% LGG-CM) or LPS did not cause any significant change in basal levels of ROS or NO production. In contrast, high concentration of LGG-CM (75% and 100%) significantly enhanced ROS generation but also significantly reduced NO level. These findings are novel and suggest for the first time that probiotics may release factors in culture which enhance ROS production and may additionally reduce deleterious effects associated with excessive nitrogen species by suppressing NO level. These events may account, in part, for the beneficial bactericidal and anti-inflammatory actions ascribed to probiotics and may be of clinical relevance.

摘要

巨噬细胞等吞噬细胞能够通过产生活性氧和氮物质来检测和杀死病原菌。巨噬细胞中自由基的形成可能受益生菌或益生菌释放但尚未鉴定的因子调控。因此,开展了相关研究以确定从GG培养物中获得的无细胞条件培养基(LGG-CM)是否能调节巨噬细胞中活性氧(ROS)和/或一氧化氮(NO)的产生。培养的J774巨噬细胞分别用HDCFDA加载以监测ROS,或用DAFFM-DA加载以检测NO。在荧光酶标仪上测量自由基产生,并通过累积和(CuSum)计算分析变化。低浓度的LGG-CM(10% LGG-CM)或LPS不会导致ROS或NO产生的基础水平发生任何显著变化。相比之下,高浓度的LGG-CM(75%和100%)显著增强了ROS的生成,但也显著降低了NO水平。这些发现是新颖的,首次表明益生菌在培养过程中可能释放出增强ROS产生的因子,并且可能通过抑制NO水平额外减少与过量氮物质相关的有害影响。这些事件可能部分解释了归因于益生菌的有益杀菌和抗炎作用,并且可能具有临床意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d117/5600347/c6522d5e23dc/gr1.jpg

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