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橄榄叶提取物,来源于 L.,通过调节小鼠巨噬细胞极化来减轻棕榈酸诱导的炎症。

Olive Leaf Extract, from L., Reduces Palmitate-Induced Inflammation via Regulation of Murine Macrophages Polarization.

机构信息

Department of Pharmacy, School of Medicine, University of Naples Federico II, 80138 Naples, Italy.

出版信息

Nutrients. 2020 Nov 28;12(12):3663. doi: 10.3390/nu12123663.

DOI:10.3390/nu12123663
PMID:33260769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7761141/
Abstract

Olive tree ( L.) leaves are an abundant source of bioactive compounds with several beneficial effects for human health. Recently, the effect of olive leaf extract in obesity has been studied. However, the molecular mechanism in preventing obesity-related inflammation has not been elucidated. Obesity is a state of chronic low-grade inflammation and is associated with an increase of pro-inflammatory M1 macrophages infiltration in the adipose tissue. In the current study, we explored L. leaf extract (OLE) anti-inflammatory activity using an in vitro model of obesity-induced inflammation obtained by stimulating murine macrophages RAW 264.7 with high dose of the free fatty acid palmitate. We found that OLE significantly suppressed the induction of pro-inflammatory mediators, tumor necrosis factor (TNF)-α, interleukin (IL)-6, IL-1β, nitric oxide (NO), prostaglandin E2 (PGE2) and reactive oxygen species (ROS), while it enhanced the anti-inflammatory cytokine, IL-10. Moreover, we demonstrated that OLE reduced the oxidative stress induced by palmitate in macrophages by regulating the NF-E2-related factor 2 (NRF2)-Kelch-like ECH-associated protein 1 (KEAP1) pathway. Finally, we showed that OLE promoted the shift of M1 macrophage toward less inflammatory M2-cells via the modulation of the associated NF-κB and proliferator-activated receptor gamma (PPARγ) signaling pathways. Thereby, our findings shed light on the potential therapeutic feature of OLE in recovering obesity-associated inflammation via regulating M1/M2 status.

摘要

油橄榄(L.)叶是生物活性化合物的丰富来源,具有多种有益于人类健康的作用。最近,研究了橄榄油提取物对肥胖的作用。然而,防止肥胖相关炎症的分子机制尚未阐明。肥胖是一种慢性低度炎症状态,与脂肪组织中促炎 M1 巨噬细胞浸润增加有关。在本研究中,我们使用由游离脂肪酸棕榈酸刺激的肥胖诱导炎症的体外模型,即刺激鼠巨噬细胞 RAW 264.7,探讨了 L.叶提取物(OLE)的抗炎活性。我们发现 OLE 可显著抑制促炎介质肿瘤坏死因子(TNF)-α、白细胞介素(IL)-6、IL-1β、一氧化氮(NO)、前列腺素 E2(PGE2)和活性氧(ROS)的诱导,同时增强抗炎细胞因子 IL-10。此外,我们证明 OLE 通过调节核因子红细胞 2 相关因子 2(NRF2)-Kelch 样 ECH 相关蛋白 1(KEAP1)途径,减轻了棕榈酸在巨噬细胞中诱导的氧化应激。最后,我们发现 OLE 通过调节相关的 NF-κB 和过氧化物酶体增殖物激活受体 γ(PPARγ)信号通路,促进 M1 巨噬细胞向炎症反应较小的 M2 细胞转变。因此,我们的研究结果表明,OLE 通过调节 M1/M2 状态,在恢复肥胖相关炎症方面具有潜在的治疗作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/cffecf55f191/nutrients-12-03663-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/47377758e965/nutrients-12-03663-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/13981f21fffa/nutrients-12-03663-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/d142a0782a04/nutrients-12-03663-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/c97014b7c734/nutrients-12-03663-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/cffecf55f191/nutrients-12-03663-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/47377758e965/nutrients-12-03663-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/13981f21fffa/nutrients-12-03663-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/d142a0782a04/nutrients-12-03663-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/c97014b7c734/nutrients-12-03663-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e815/7761141/cffecf55f191/nutrients-12-03663-g005.jpg

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