首页> 美国卫生研究院文献>other >Palmitoylethanolamide Modulates Inflammation-Associated Vascular Endothelial Growth Factor (VEGF) Signaling via the Akt/mTOR Pathway in a Selective Peroxisome Proliferator-Activated Receptor Alpha (PPAR-α)-Dependent Manner
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Palmitoylethanolamide Modulates Inflammation-Associated Vascular Endothelial Growth Factor (VEGF) Signaling via the Akt/mTOR Pathway in a Selective Peroxisome Proliferator-Activated Receptor Alpha (PPAR-α)-Dependent Manner

机译:棕榈酰乙醇酰胺通过选择性过氧化物酶体增殖物激活受体α(PPAR-α)依赖的方式通过Akt / mTOR途径调节炎症相关的血管内皮生长因子(VEGF)信号。

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摘要

Background and AimAngiogenesis is emerging as a pivotal process in chronic inflammatory pathologies, promoting immune infiltration and prompting carcinogenesis. Ulcerative Colitis (UC) and Crohn’s Disease (CD) represent paradigmatic examples of intestinal chronic inflammatory conditions in which the process of neovascularization correlates with the severity and progression of the diseases. Molecules able to target the angiogenesis have thus the potential to synergistically affect the disease course. Beyond its anti-inflammatory effect, palmitoylethanolamide (PEA) is able to reduce angiogenesis in several chronic inflammatory conditions, but no data about its anti-angiogenic activity in colitis have been produced, yet.
机译:背景和目的血管生成正在成为慢性炎性病理学中的关键过程,其促进免疫浸润并促进癌变。溃疡性结肠炎(UC)和克罗恩氏病(CD)代表了肠道慢性炎症的典型例子,其中新血管形成的过程与疾病的严重程度和进展相关。能够靶向血管生成的分子因此具有协同影响疾病进程的潜力。棕榈酰乙醇酰胺(PEA)除了具有抗炎作用外,还能够在几种慢性炎症条件下减少血管生成,但尚未产生有关其在结肠炎中抗血管生成活性的数据。

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