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通过藜麦种子 4'-香叶基阿魏酸提取物的生物活性调节 HCT116 细胞系中 CAT-2B 介导的 l-精氨酸摄取和一氧化氮生物合成。

Modulation of CAT-2B-Mediated l-Arginine Uptake and Nitric Oxide Biosynthesis in HCT116 Cell Line Through Biological Activity of 4'-Geranyloxyferulic Acid Extract from Quinoa Seeds.

机构信息

Department of Psychological, Health and Territorial Sciences, University G. D'Annunzio, 66100 Chieti, Italy.

Department of Medicine and Science of Aging, University G. D'Annunzio, 66100 Chieti, Italy.

出版信息

Int J Mol Sci. 2019 Jul 2;20(13):3262. doi: 10.3390/ijms20133262.

Abstract

is a "pseudocereal" grain which attracts a lot of attention in the scientific community as it has a positive effect on health. Here, we investigate the presence of biologically active O-prenylated phenylpropanoids in the ethanol extract of commercially available quinoa seeds. We claim that 4'-Geranyloxyferulic acid (GOFA) was the only phytochemical product found that belongs to quinoa's group secondary metabolites. We studied the changes in the oxidative and inflammatory status of the cellular environment in HCT 116 cell line processed with quinoa extract and its component GOFA; the implementation was done through the analysis of the antioxidant enzymes (SOD and CAT), the pro-inflammatory components (iNOS, IL-6 and TNF-α), and the products of intermediary metabolism (ONOO, O). Moreover, the l-arginine uptake was proposed as a target of the tested compounds. We demonstrated that the GOFA, through a decrease of the CAT-2B expression, leads to a reduction of the l-arginine uptake, downregulating the harmful iNOS and restoring the altered redox state. These results propose a new molecular target involved in the reduction of the critical inflammatory process responsible for the cancer progression.

摘要

是一种“伪谷物”,由于其对健康有积极影响,因此在科学界引起了广泛关注。在这里,我们研究了市售藜麦种子的乙醇提取物中是否存在具有生物活性的 O-香叶基化苯丙素类化合物。我们声称,4'-香叶基阿魏酸(GOFA)是唯一发现属于藜麦类次生代谢产物的植物化学产物。我们研究了用藜麦提取物及其成分 GOFA 处理的 HCT 116 细胞系中细胞环境的氧化和炎症状态的变化;通过分析抗氧化酶(SOD 和 CAT)、促炎成分(iNOS、IL-6 和 TNF-α)和中间代谢产物(ONOO、O)来实现。此外,还提出了 l-精氨酸摄取作为测试化合物的靶标。我们证明,GOFA 通过降低 CAT-2B 的表达,导致 l-精氨酸摄取减少,下调有害的 iNOS 并恢复改变的氧化还原状态。这些结果提出了一个新的分子靶标,涉及减少负责癌症进展的关键炎症过程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afe9/6650945/84be3072b691/ijms-20-03262-g001.jpg

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