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某植物叶片碱性提取物抗炎作用的多组学分析

Multi-Omics Analysis of Anti-Inflammatory Action of Alkaline Extract of the Leaves of sp.

作者信息

Sakagami Hiroshi, Nakatani Sachie, Enomoto Ayame, Ota Sana, Kaneko Miku, Sugimoto Masahiro, Horiuchi Misaki, Toeda Kazuki, Oizumi Takaaki

机构信息

Meikai University Research Institute of Odontology (M-RIO), Meikai University School of Dentistry, 1-1 Keyakidai, Sakado, Saitama 350-0283, Japan.

Graduate School of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan.

出版信息

J Clin Med. 2021 May 13;10(10):2100. doi: 10.3390/jcm10102100.

DOI:10.3390/jcm10102100
PMID:34068182
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8152990/
Abstract

Efficient utilization of alkaline extracts of several plants for the treatment of oral diseases has been reported. To investigate the mechanism of anti-inflammatory activity of alkaline extract of the leaves of sp. (SE), multi-omics analysis using metabolomics and DNA array was performed. Human gingival fibroblasts (HGFs) were treated for IL-1β to induce inflammation (detected by PGE production in culture medium) in the presence or absence of SE. Both IL-1β and SE showed slight hormetic growth stimulation against HGF. SE inhibited PGE production dose- and time-dependently. Its inhibitory action was more pronounced by first treating the cells with SE, rather than with IL-1β. At 3 h after IL-1β treatment, 18 amino acids (except cysteine and glutamic acid), total glutathione (GSH, GSSG, Cys-GSH disulfide), Met-sulfoxide, 5-oxoproline, and SAM declined, whereas DNA expressions of AKT, CASP3, and CXCL3 were elevated. These changes were reversed by simultaneous treatment with SE. The present study suggests that the anti-inflammatory action of SE is mediated via various metabolic pathways for cell survival, apoptosis, and leukocyte recruitment.

摘要

已有报道称几种植物的碱性提取物可有效用于治疗口腔疾病。为了研究某植物叶片碱性提取物(SE)的抗炎活性机制,进行了代谢组学和DNA阵列的多组学分析。在有或无SE存在的情况下,用人牙龈成纤维细胞(HGF)处理白细胞介素-1β(IL-1β)以诱导炎症(通过培养基中前列腺素E的产生来检测)。IL-1β和SE对HGF均表现出轻微的刺激生长效应。SE剂量和时间依赖性地抑制前列腺素E的产生。通过先用SE而非IL-1β处理细胞,其抑制作用更为明显。在IL-1β处理3小时后,18种氨基酸(除半胱氨酸和谷氨酸外)、总谷胱甘肽(GSH、GSSG、半胱氨酸-谷胱甘肽二硫化物)、甲硫氨酸亚砜、5-氧代脯氨酸和S-腺苷甲硫氨酸下降,而AKT、CASP3和CXCL3的DNA表达升高。同时用SE处理可逆转这些变化。本研究表明,SE的抗炎作用是通过细胞存活、凋亡和白细胞募集的各种代谢途径介导的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/a8530438d020/jcm-10-02100-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/77b273ffe843/jcm-10-02100-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/e64e9b77535a/jcm-10-02100-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/daec53861bcf/jcm-10-02100-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/62d3fd941d70/jcm-10-02100-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/a8530438d020/jcm-10-02100-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/77b273ffe843/jcm-10-02100-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/e64e9b77535a/jcm-10-02100-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/daec53861bcf/jcm-10-02100-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/62d3fd941d70/jcm-10-02100-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d17/8152990/a8530438d020/jcm-10-02100-g005.jpg

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