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Phlorotannins with Potential Anti-tyrosinase and Antioxidant Activity Isolated from the Marine Seaweed Ecklonia stolonifera

机译:具有潜在的抗酪氨酸酶和抗氧化活性的抗酪氨酸和抗氧化活性从海藻海藻塞克隆岛分离

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摘要

Compounds were isolated from Ecklonia stolonifera Okamura, a marine brown alga widely consumed as food. Among the isolated compounds, 974-A was demonstrated for the first time to be a potent competitive inhibitor of mushroom tyrosinase activity towards l-tyrosine and l-DOPA (IC50 values = 1.57 ± 0.08 and 3.56 ± 0.22 µM, respectively). Molecular docking simulations clarified that the hydroxyl residues of the isolated compounds formed hydrogen bonds with residues at the catalytic and allosteric sites of tyrosinase, while other residues participated in hydrophobic interactions. Moreover, 974-A, phlorofucofuroeckol-A and eckol reduced the cellular melanin content and tyrosinase activity, and downregulated the expression of melanogenesis enzymes including tyrosinase, tyrosinase-related protein (TRP)-1, and TRP-2 in B16F10 melanoma cells. These compounds also effectively scavenged radicals at the cellular level. Thus, our results revealed that compounds isolated from E. stolonifera are potent tyrosinase inhibitors with potential applications in the cosmetic industry for treatment of hyperpigmentation and for the anti-browning effect in the agricultural field.
机译:从Ecklonia Stolonifera Okamura分离化合物,作为食物广泛消费的海洋棕色藻类。在分离的化合物中,第一次证明974-A分别对L-酪氨酸和L-DOPA(IC 50值= 1.57±0.08和3.56±0.22μm)是蘑菇酪氨酸酶活性的有效竞争性抑制剂。分子对接模拟阐明了分离的化合物的羟基残基与酪氨酸酶的催化​​和变构位点的残基形成氢键,而其他残基参与疏水相互作用。此外,974-A,甘油琥珀猴粥样醇-A和ECKOL降低了细胞黑色素含量和酪氨酸酶活性,并下调了B16F10黑色素瘤细胞中酪氨酸酶,酪氨酸酶相关蛋白(TRP)和TRP-2在内的糖素生成酶的表达。这些化合物在细胞水平下也有效地清除了自由基。因此,我们的结果表明,从E.Stolonifera中分离的化合物是具有潜在应用的高效酪氨酸酶抑制剂,在化妆品行业中进行治疗过度沉想和农业领域的抗褐变效应。

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