Department of Biochemistry, Universidade Federal do Rio Grande do Norte, Natal, Rio Grande do Norte 59.078-970, Brazil.
Department of Biochemistry, Universidade Federal de Juiz de Fora, Juiz de Fora, Minas Gerais 36036-900, Brazil.
Mar Drugs. 2019 Aug 28;17(9):506. doi: 10.3390/md17090506.
Some antioxidant compounds decrease the amount of intracellular reactive oxygen species (ROS) and consequently reduce the deleterious effects of ROS in osteoblasts. Thus, these compounds fight against osteoporosis. Brown seaweeds are a rich source of antioxidant fucose-containing sulfated polysaccharides (fucans and fucoidans). We obtained six fucoidans (FRFs)-F0.3, F0.5, F0.7, F1.0, F1.5, and F2.1-from by proteolytic digestion followed by sequential acetone precipitation. Except for F0.3, all FRFs showed antioxidant activity in different in vitro tests. In pre- osteoblast-like cells (MC3T3-L1) exposed to HO-oxidative stress, caspase-3 and caspase-9 were activated, resulting in apoptosis of the cells. We also observed a decrease in superoxide dismutase (SOD) and alkaline phosphatase (ALP) activity. The antioxidant FRFs protected the cells from the oxidative damage caused by HO, decreasing intracellular ROS and caspase activation, and increasing SOD activity. The most effective protection against damage was provided by F0.7, F1.5, and F2.1. At 0.5 mg/mL, these FRFs also suppressed the HO-mediated inhibition of ALP activity. The data indicated that FRFs F0.7, F1.5, and F2.1 from were antioxidants that protected bone tissue from oxidative stress and could represent possible adjuvants for the treatment of bone fragility through counteracting oxidative phenomena.
一些抗氧化化合物可以减少细胞内活性氧物质 (ROS) 的含量,从而减少 ROS 对成骨细胞的有害影响。因此,这些化合物可以对抗骨质疏松症。褐藻是一种富含抗氧化性含岩藻糖硫酸多糖(褐藻糖胶和褐藻胶)的来源。我们通过蛋白水解消化后,再经过连续的丙酮沉淀,从 中获得了六种褐藻糖胶(FRFs)-F0.3、F0.5、F0.7、F1.0、F1.5 和 F2.1。除了 F0.3 之外,所有 FRFs 在不同的体外试验中均表现出抗氧化活性。在受到 HO 氧化应激的前成骨样细胞(MC3T3-L1)中,半胱天冬酶-3 和半胱天冬酶-9 被激活,导致细胞凋亡。我们还观察到超氧化物歧化酶 (SOD) 和碱性磷酸酶 (ALP) 活性下降。抗氧化性 FRFs 可保护细胞免受 HO 引起的氧化损伤,减少细胞内 ROS 和半胱天冬酶的激活,并增加 SOD 活性。F0.7、F1.5 和 F2.1 对损伤的保护作用最为有效。在 0.5mg/mL 时,这些 FRFs 还抑制了 HO 介导的 ALP 活性抑制。数据表明,FRFs F0.7、F1.5 和 F2.1 是可以保护骨组织免受氧化应激的抗氧化剂,并且可以通过对抗氧化现象来代表治疗骨脆弱性的可能辅助剂。