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食用红巨藻 Sarcodia ceylanica 的乙酸乙酯部分的抗炎和镇痛作用。

Anti-Inflammatory and Antinociceptive Effects of Ethyl Acetate Fraction of an Edible Red Macroalgae Sarcodia ceylanica.

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 80424, Taiwan.

Department of Marketing and Distribution Management, Fortune Institute of Technology, Kaohsiung 83158, Taiwan.

出版信息

Int J Mol Sci. 2017 Nov 17;18(11):2437. doi: 10.3390/ijms18112437.

Abstract

Research so far has only shown that edible red macroalgae, has the ability to eliminate free radicals and anti-diabetic, anti-bacterial properties. This study was conducted both in vitro and in vivo on the ethyl acetate extract (PD1) of farmed red macroalgae in order to explore its anti-inflammatory properties. In order to study the in vitro anti-inflammatory effects of PD1, we used lipopolysaccharide (LPS) to induce inflammatory responses in murine macrophages. For evaluating the potential in vivo anti-inflammatory and antinociceptive effects of PD1, we used carrageenan-induced rat paw edema to produce inflammatory pain. The in vitro results indicated that PD1 inhibited the LPS-induced pro-inflammatory protein, inducible nitric oxide synthase (iNOS) in macrophages. Oral PD1 can reduce carrageenan-induced paw edema and inflammatory nociception. PD1 can significantly inhibit carrageenan-induced leukocyte infiltration, as well as the protein expression of inflammatory mediators (iNOS, interleukin-1β, and myeloperoxidase) in inflammatory tissue. The above results indicated that PD1 has great potential to be turned into a functional food or used in the development of new anti-inflammatory and antinociceptive agents. The results from this study are expected to help scientists in the continued development of for other biomedical applications.

摘要

迄今为止的研究仅表明,可食用的红色大型藻类具有消除自由基和抗糖尿病、抗菌的特性。本研究对养殖红色大型藻类的乙酸乙酯提取物(PD1)进行了体外和体内研究,以探索其抗炎特性。为了研究 PD1 的体外抗炎作用,我们使用脂多糖(LPS)诱导小鼠巨噬细胞产生炎症反应。为了评估 PD1 的潜在体内抗炎和抗伤害感受作用,我们使用角叉菜胶诱导大鼠足肿胀产生炎症性疼痛。体外结果表明,PD1 抑制了 LPS 诱导的巨噬细胞中促炎蛋白诱导型一氧化氮合酶(iNOS)的表达。口服 PD1 可以减轻角叉菜胶诱导的足肿胀和炎症性伤害感受。PD1 可显著抑制角叉菜胶诱导的白细胞浸润,以及炎症组织中炎症介质(iNOS、白细胞介素-1β和髓过氧化物酶)的蛋白表达。上述结果表明,PD1 具有很大的潜力,可以转化为功能性食品或用于开发新的抗炎和抗伤害感受药物。本研究的结果有望帮助科学家继续开发用于其他生物医学应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b89a/5713404/c5a19cd1e19c/ijms-18-02437-g001a.jpg

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