Department of Seafood Science, National Kaohsiung Marine University, No. 142, Haijhuan Rd., Nanzih District, Kaohsiung 81157, Taiwan.
Molecules. 2017 Dec 29;23(1):78. doi: 10.3390/molecules23010078.
In this study, a compressional-puffing process (CPP) was used to pretreat (SH) and then fucoidan was extracted from SH by hot water. Three fucoidan extracts, namely SH1 (puffing at 0 kg/cm²); SH2 (puffing at 1.7 kg/cm²); and SH3 (puffing at 10.0 kg/cm²) were obtained, and their compositions and biological activities were evaluated. The results indicate that CPP increased the extraction yield, total sugar content, and molar ratios of sulfate/fucose of fucoidan and decreased molecular weight and impurities of fucoidan. The SH1-SH3 extracts exhibited characteristics of fucoidan as demonstrated by the analyses of composition, FTIR spectroscopy, NMR spectroscopy, and molecular weight. All SH1-SH3 extracts showed antioxidant activities. The SH1-SH3 extracts protected SH-SY5Y cells from 6-hydroxydopamine (6-OHDA)-induced apoptosis as illustrated by cell cycle distribution, cytochrome c release, activation of caspase-8, -9, and -3, and DNA fragmentation analyses. Additional experiments revealed that phosphorylation of Akt is involved in the opposing effects of SH1-SH3 on 6-OHDA-induced neurotoxicity. SH3 exhibited a relatively high extraction yield, the lowest levels of impurities, and was the most effective at reversing the 6-OHDA-induced neurotoxicity of SH-SY5Y cells among SH1-SH3, which taken together indicate that it may have potential as a candidate therapeutic agent for the preventive therapy of neurodegenerative diseases.
在这项研究中,采用压缩膨化法(CPP)对海带(SH)进行预处理,然后用热水从 SH 中提取褐藻糖胶。得到了三种褐藻糖胶提取物,即 SH1(膨化压力为 0 kg/cm²);SH2(膨化压力为 1.7 kg/cm²);和 SH3(膨化压力为 10.0 kg/cm²),并评价了它们的组成和生物活性。结果表明,CPP 提高了褐藻糖胶的提取产率、总糖含量和硫酸根/岩藻糖摩尔比,降低了褐藻糖胶的分子量和杂质。SH1-SH3 提取物具有褐藻糖胶的特征,这从组成分析、FTIR 光谱、NMR 光谱和分子量得到证实。所有 SH1-SH3 提取物均表现出抗氧化活性。SH1-SH3 提取物通过细胞周期分布、细胞色素 c 释放、半胱天冬酶-8、-9 和 -3 的激活以及 DNA 片段化分析,保护 SH-SY5Y 细胞免受 6-羟多巴胺(6-OHDA)诱导的凋亡。进一步的实验表明,Akt 的磷酸化参与了 SH1-SH3 对 6-OHDA 诱导的神经毒性的拮抗作用。SH3 具有较高的提取产率、最低水平的杂质,对 SH-SY5Y 细胞 6-OHDA 诱导的神经毒性的逆转作用最为有效,这表明它可能有潜力作为神经退行性疾病预防治疗的候选治疗剂。