K. Spyridopoulou, Georgios Aindelis, Georgia Kolezaki, A. Tiptiri-Kourpeti, K. Chlichlia
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引用次数: 0
Abstract
Mastic oil (MO) is extracted from the resin of the bark of Pistacia lentiscus var. chia, a tree abundantly grown in the Greek island of Chios. Various biological activities, such as antimicrobial, anticancer and antioxidant, have been associated with the dietary intake of MO. However, little is known about MO’s potential anti-inflammatory effects, while some of its main chemical constituents were reported to exert significant anti-inflammatory activity. This study aims to assay the bioactivity of MO on in vitro and in vivo experimental inflammation models, in particular on LPS-stimulated RAW264.7 macrophages, murine primary peritoneal macrophages and a model of zymosan-induced peritonitis in BALB/c mice. The per os administration of MO inhibited the recruitment of macrophages into the peritoneal cavity of zymosan-treated mice, but did not affect neutrophil mobilisation or the levels of IL-6 or TNF-α in the peritoneal fluid. Similarly, IL-6 and TNF-α secretion in primary LPS-stimulated macrophages was not affected by MO, but the levels of phosphoproteins that activate inflammation in macrophages were differentially regulated. Finally, MO and some of its individual constituents reduced nitric oxide (NO), prostaglandin E2 and TNF-α levels in supernatants of LPS-stimulated RAW264.7 cells and inhibited their phagocytosis rate. Our data imply that MO may promote an anti-inflammatory transition in macrophages due to the combined bioactivities of its individual constituents. Thus, as a mixture of various compounds, MO seems to affect multiple molecular mechanisms that are involved in the development of inflammation. Therefore, more research, focusing on MO’s individual constituents and employing various pre-clinical inflammation models that activate different mechanisms, is required for a detailed investigation of the oil’s potential anti-inflammatory activity.
乳胶油(MO)是从黄松木(Pistacia lentiscus vara . chia)树皮的树脂中提取出来的,黄松木生长在希腊的希俄斯岛(Chios)。各种生物活性,如抗菌、抗癌和抗氧化,都与膳食摄入相关联。然而,对MO的潜在抗炎作用知之甚少,而其一些主要化学成分被报道具有显著的抗炎活性。本研究旨在检测MO对体外和体内实验炎症模型的生物活性,特别是对lps刺激的RAW264.7巨噬细胞、小鼠原代腹膜巨噬细胞和酶生蛋白诱导的BALB/c小鼠腹膜炎模型的生物活性。注射MO可抑制巨噬细胞向腹腔募集,但不影响中性粒细胞动员,也不影响腹膜液中IL-6或TNF-α的水平。同样,原代lps刺激的巨噬细胞中IL-6和TNF-α的分泌不受MO的影响,但巨噬细胞中激活炎症的磷酸化蛋白水平受到差异调节。最后,MO及其部分成分可降低lps刺激RAW264.7细胞上清液中一氧化氮(NO)、前列腺素E2和TNF-α水平,抑制其吞噬率。我们的数据表明,由于其单个成分的联合生物活性,MO可能促进巨噬细胞的抗炎转变。因此,作为多种化合物的混合物,MO似乎影响了参与炎症发展的多种分子机制。因此,需要更多的研究,关注油的单个成分,并采用各种临床前炎症模型来激活不同的机制,以详细研究油的潜在抗炎活性。