Tomas-Hernandez Sarah, Blanco Jordi, Garcia-Vallvé Santiago, Pujadas Gerard, Ojeda-Montes María José, Gimeno Aleix, Arola Lluís, Minghetti Luisa, Beltrán-Debón Raúl, Mulero Miquel
Cheminformatics and Nutrition Group, Department of Biochemistry and Biotechnology, Campus Sescelades, Universitat Rovira i Virgili (URV), 43007 Tarragona, Catalonia, Spain.
Physiology Unit, Laboratory of Toxicology and Environmental Health, Research in Neurobehavior and Health (NEUROLAB), School of Medicine, IISPV, Universitat Rovira i Virgili (URV), 43202 Tarragona, Catalonia, Spain.
Pharmaceutics. 2021 May 28;13(6):806. doi: 10.3390/pharmaceutics13060806.
In response to foreign or endogenous stimuli, both microglia and astrocytes adopt an activated phenotype that promotes the release of pro-inflammatory mediators. This inflammatory mechanism, known as neuroinflammation, is essential in the defense against foreign invasion and in normal tissue repair; nevertheless, when constantly activated, this process can become detrimental through the release of neurotoxic factors that amplify underlying disease. In consequence, this study presents the anti-inflammatory and immunomodulatory properties of -orsellinaldehyde, a natural compound found by an in silico approach in the mushroom, in astrocytes and microglia cells. For this purpose, primary microglia and astrocytes were isolated from mice brain and cultured in vitro. Subsequently, cells were exposed to LPS in the absence or presence of increasing concentrations of this natural compound. Specifically, the results shown that -orsellinaldehyde strongly inhibits the LPS-induced inflammatory response in astrocytes and microglia by decreasing nitrite formation and downregulating iNOS and HO-1 expression. Furthermore, in microglia cells -orsellinaldehyde inhibits NF-κB activation; and potently counteracts LPS-mediated p38 kinase and JNK phosphorylation (MAPK). In this regard, -orsellinaldehyde treatment also induces a significant cell immunomodulation by repolarizing microglia toward the M2 anti-inflammatory phenotype. Altogether, these results could partially explain the reported beneficial effects of extracts on inflammatory conditions.
对外源性或内源性刺激的反应中,小胶质细胞和星形胶质细胞都会呈现出一种激活的表型,这种表型会促进促炎介质的释放。这种炎症机制,即神经炎症,对于抵御外来入侵和正常组织修复至关重要;然而,当持续激活时,这个过程可能会通过释放放大潜在疾病的神经毒性因子而变得有害。因此,本研究展示了苔黑醛(一种通过计算机方法在蘑菇中发现的天然化合物)在星形胶质细胞和小胶质细胞中的抗炎和免疫调节特性。为此,从小鼠大脑中分离出原代小胶质细胞和星形胶质细胞并进行体外培养。随后,在不存在或存在浓度递增的这种天然化合物的情况下,将细胞暴露于脂多糖(LPS)。具体而言,结果表明苔黑醛通过减少亚硝酸盐形成以及下调诱导型一氧化氮合酶(iNOS)和血红素加氧酶 - 1(HO - 1)的表达,强烈抑制LPS诱导的星形胶质细胞和小胶质细胞中的炎症反应。此外,在小胶质细胞中,苔黑醛抑制核因子κB(NF - κB)的激活;并有效对抗LPS介导的p38激酶和应激活化蛋白激酶(JNK)磷酸化(丝裂原活化蛋白激酶,MAPK)。在这方面,苔黑醛处理还通过使小胶质细胞重新极化至M2抗炎表型诱导显著的细胞免疫调节。总之,这些结果可以部分解释所报道的提取物对炎症状况的有益作用。