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口服 Phlorotannins 可抑制化学介质释放和环氧化酶-2 信号通路,缓解小鼠耳肿胀。

Orally Administered Phlorotannins from Suppress Chemical Mediator Release and Cyclooxygenase-2 Signaling to Alleviate Mouse Ear Swelling.

机构信息

Laboratory of Food Function and Biochemistry, Department of Food Science and Technology, National Research and Development Agency, Japan Fisheries Research and Education Agency, National Fisheries University, Shimonoseki 759-6595, Japan.

Laboratory of Bioorganic Chemistry, Graduate School of Bioresources, Mie University, Tsu 514-8507, Japan.

出版信息

Mar Drugs. 2018 Aug 2;16(8):267. doi: 10.3390/md16080267.

Abstract

Phlorotannin is the collective term for polyphenols derived from brown algae belonging to the genera , , , and etc. Since the incidence of allergies is currently increasing in the world, there is a focus on phlorotannins having anti-allergic and anti-inflammatory effects. In this study, six purified phlorotannins (eckol; 6,6'-bieckol; 6,8'-bieckol; 8,8'-bieckol; phlorofucofuroeckol (PFF)-A and PFF-B) from , orally administered to mice, were examined for their suppression effects on ear swelling. In considering the suppression, we also examined whether the phlorotannins suppressed release of chemical mediators (histamine, leukotriene B₄ and prostaglandin E₂), and mRNA expression and/or the activity of cyclooxygenase-2 (COX-2), using RBL-2H3 cells, a cultured mast cell model. Results showed that the phlorotnannins exhibited suppression effects in all experiments, with 6,8'-bieckol, 8,8'-bieckol and PFF-A showing the strongest of these effects. In conclusion, orally administered phlorotannins suppress mouse ear swelling, and this mechanism apparently involves suppression of chemical mediator release and COX-2 mRNA expression or activity. This is the first report of the anti-allergic effects of the orally administered purified phlorotannins in vivo. Phlorotannins show potential for use in functional foods or drugs.

摘要

岩藻黄质是一类多酚物质的统称,来源于属于 、 、 、 和 等属的褐藻。由于目前全世界的过敏发病率不断增加,人们开始关注岩藻黄质具有抗过敏和抗炎作用。在这项研究中,我们将从 中提取的六种纯化岩藻黄质(岩藻依醇;6,6'-双岩藻依醇;6,8'-双岩藻依醇;8,8'-双岩藻依醇;岩藻福枯双酚-A 和岩藻福枯双酚-B)经口给予小鼠,以研究其对耳部肿胀的抑制作用。在考虑抑制作用时,我们还使用 RBL-2H3 细胞(一种培养的肥大细胞模型),检测了岩藻黄质是否抑制化学介质(组胺、白三烯 B₄ 和前列腺素 E₂)的释放,以及环氧化酶-2(COX-2)的 mRNA 表达和/或活性。结果表明,岩藻黄质在所有实验中均表现出抑制作用,其中 6,8'-双岩藻依醇、8,8'-双岩藻依醇和岩藻福枯双酚-A 的抑制作用最强。综上所述,口服岩藻黄质可抑制小鼠耳部肿胀,其机制显然涉及抑制化学介质释放和 COX-2 mRNA 表达或活性。这是首次报道口服纯化岩藻黄质在体内具有抗过敏作用。岩藻黄质有望用于功能性食品或药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c888/6117712/3447e570e01a/marinedrugs-16-00267-g001.jpg

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