Stefanon Bruno, Colitti Monica
Department of Scienze Agroalimentari, Ambientali e Animali, University of Udine, Udine 33100, Italy.
Department of Scienze Agroalimentari, Ambientali e Animali, University of Udine, Udine 33100, Italy
Exp Biol Med (Maywood). 2016 Oct;241(16):1796-802. doi: 10.1177/1535370216654226. Epub 2016 Jun 10.
Hydroxytyrosol has various pharmacological properties, including anti-oxidative stress and anti-inflammatory activities, preventing hyperglycemia, insulin resistance, and the metabolic syndrome. The present study is focused on the anti-adipogenic and lipolytic activity of hydroxytyrosol on primary human visceral adipocytes. Pre-adipocytes were analyzed after 10 (P10) and 20 (P20) days of treatment during differentiation and after 7 (A7) days of treatment when they reached mature shape. The treatment with hydroxytyrosol extract significantly (P < 0.001) increased apoptosis in P10 and P20 cells in comparison to control and A7 cells; significantly (P < 0.001) reduced triglyceride accumulation in P20 cells compared to P10 and control cells; and significantly (P < 0.001) increased lipolysis in P20 cells in comparison to control cells and A7 mature adipocytes. Hydroxytyrosol-treated P20 cells significantly (P < 0.05) increased expression of genes involved in inhibition of adipogenesis, such as GATA2, GATA3, WNT3A, SFRP5, HES1, and SIRT1. In contrast, genes involved in promoting adipogenesis such as LEP, FGF1, CCND1, and SREBF1 were significantly down-regulated by hydroxytyrosol treatment. These data suggest that hydroxytyrosol promotes lipolysis and apoptotic activity in primary human visceral pre-adipocytes during differentiation and does not affect already mature adipocytes.
羟基酪醇具有多种药理特性,包括抗氧化应激和抗炎活性,可预防高血糖、胰岛素抵抗和代谢综合征。本研究聚焦于羟基酪醇对原代人内脏脂肪细胞的抗脂肪生成和脂解活性。在分化过程中,对前脂肪细胞进行10天(P10)和20天(P20)的处理后,以及在它们达到成熟形态后进行7天(A7)的处理后进行分析。与对照细胞和A7细胞相比,羟基酪醇提取物处理显著(P < 0.001)增加了P10和P20细胞的凋亡;与P10细胞和对照细胞相比,显著(P < 0.001)减少了P20细胞中甘油三酯的积累;与对照细胞和A7成熟脂肪细胞相比,显著(P < 0.001)增加了P20细胞的脂解。经羟基酪醇处理的P20细胞显著(P < 0.05)增加了参与抑制脂肪生成的基因的表达,如GATA2、GATA3、WNT3A、SFRP5、HES1和SIRT1。相反,经羟基酪醇处理后,参与促进脂肪生成的基因如LEP、FGF1、CCND1和SREBF1显著下调。这些数据表明,羟基酪醇在分化过程中促进原代人内脏前脂肪细胞的脂解和凋亡活性,而不影响已经成熟的脂肪细胞。