Lee Dahae, Kim Ji-Young, Qi Yutong, Park Sangsu, Lee Hye Lim, Yamabe Noriko, Kim Hocheol, Jang Dae Sik, Kang Ki Sung
College of Korean Medicine, Gachon University, Seongnam 13120, South Korea.
Department of Life and Nanopharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul 02447, South Korea.
Bioorg Med Chem Lett. 2021 Oct 1;49:128326. doi: 10.1016/j.bmcl.2021.128326. Epub 2021 Aug 14.
Flowers of Prunus persica (L.) Batsch (Rosaceae), known as peach blossoms, have been reported to exert anti-obesity effects by improving hepatic lipid metabolism in obese mice. However, little is known regarding the anti-adipogenic effects of the phenolic compounds isolated from P. persica flowers. This study investigated the inhibitory effects of compounds extracted from P. persica flowers (PPF) on adipogenesis in 3T3-L1 murine preadipocytes using adipogenic differentiation assays. Additionally, we compared the anti-adipogenic effects of the phenolic compounds isolated from PPF, such as prunasin amide (1), amygdalin amide (2), prunasin acid (3), mandelamide (4), methyl caffeate (5), ferulic acid (6), chlorogenic acid (7), benzyl α-l-xylpyranosyl-(1 → 6)-β-d-glucopyranoside (8), prunin (9), naringenin (10), nicotiflorin (11), astragalin (12), afzelin (13), and uridine (14), on adipogenesis in 3T3-L1 murine preadipocytes. PPF and compounds 4-7 and 10 significantly inhibited adipogenesis. Among them, mandelamide (4) exhibited the maximum inhibitory activity with an IC of 36.04 ± 1.82 μM. Additionally, mandelamide downregulated the expression of key adipogenic markers, such as extracellular signal-regulated kinase, c-Jun-N-terminal kinase, P38, CCAAT/enhancer-binding protein α, CCAAT/enhancer-binding protein β, peroxisome proliferator activated receptor γ, and glucocorticoid receptor. These results indicate that mandelamide is an active ingredient of PPF possessing anti-obesity properties.
蔷薇科植物桃(Prunus persica (L.) Batsch)的花,即桃花,据报道可通过改善肥胖小鼠的肝脏脂质代谢发挥抗肥胖作用。然而,关于从桃花中分离出的酚类化合物的抗脂肪生成作用知之甚少。本研究使用脂肪生成分化试验,研究了从桃花(PPF)中提取的化合物对3T3-L1小鼠前脂肪细胞脂肪生成的抑制作用。此外,我们比较了从PPF中分离出的酚类化合物,如苦杏仁苷酰胺(1)、苦杏仁苷酰胺(2)、苦杏仁酸(3)、扁桃酰胺(4)、咖啡酸甲酯(5)、阿魏酸(6)、绿原酸(7)、苄基α-L-木糖吡喃糖基-(1→6)-β-D-吡喃葡萄糖苷(8)、樱草糖苷(9)、柚皮素(10)、烟花苷(11)、紫云英苷(12)、阿夫泽林(13)和尿苷(14),对3T3-L1小鼠前脂肪细胞脂肪生成的抗脂肪生成作用。PPF以及化合物4-7和10显著抑制脂肪生成。其中,扁桃酰胺(4)表现出最大抑制活性,IC50为36.04±1.82μM。此外,扁桃酰胺下调了关键脂肪生成标志物的表达,如细胞外信号调节激酶、c-Jun氨基末端激酶、P38、CCAAT/增强子结合蛋白α、CCAAT/增强子结合蛋白β、过氧化物酶体增殖物激活受体γ和糖皮质激素受体。这些结果表明,扁桃酰胺是PPF中具有抗肥胖特性的活性成分。