Truong Thi Phuong Thao, Tran Thanh Men, Dai Thi Xuan Trang, Tran Chi Linh
Department of Biology, College of Natural Sciences, Can Tho University, 94000, Viet Nam.
J Tradit Complement Med. 2023 Mar 20;13(4):408-416. doi: 10.1016/j.jtcme.2023.03.007. eCollection 2023 Jul.
Brown algae () extract (DP) presented high inhibitory potential against α-amylase. The present study aims to isolate, purify and evaluate the antihyperglycemic and anti-type 2 diabetic activities of marine hydroquinone from DP.
Marine hydroquinones were isolated using silica gel, HPLC, and NMR spectroscopy was used to identify compound 1 and compound 2 as zonarol and isozonarol, respectively. The anti-hyperglycemic and anti-type 2 diabetic activities of zonarol were investigated by assay (α-amylase, α-glucosidase), Lineweaver-Burk plot and Type 2 diabetes mellitus model (T2DM) mice induced by streptozotocin (STZ).
Zonarol had the highest content and the strongest inhibitory activity against α-glucosidase (IC value of 6.03 mg L) and α-amylase (IC value of 19.29 mg L) in a competitive inhibition and mix-type manner, respectively. The maltose and starch loading tests revealed that zonarol significantly reduced postprandial glycemia after 30 min loading (9.12 and 8.12 mg/dL, respectively), compared to normal (11.37 and 12.37 mg/dL, respectively). Zonarol exhibited pancreatic islet cell rejuvenation, as evidenced by increased pancreatic islet mass, and hence helps in the restoration of insulin levels and therefore improves the glucose metabolism in STZ-induced diabetic mice. Zonarol treatment in T2DM elevated abundant levels of main SCFAs (propionate, butyrate, and valeric acid), which are closely related to glucose metabolism homeostasis.
Our finding indicates that zonarol could be used as a food supplement to treat hyperglycemia and diabetes.
褐藻提取物(DP)对α-淀粉酶具有较高的抑制潜力。本研究旨在从DP中分离、纯化并评估海洋对苯二酚的降血糖和抗2型糖尿病活性。
采用硅胶柱色谱法分离海洋对苯二酚,利用高效液相色谱法(HPLC)和核磁共振光谱法(NMR)分别鉴定化合物1和化合物2为聚马酚和异聚马酚。通过体外实验(α-淀粉酶、α-葡萄糖苷酶)、Lineweaver-Burk作图法以及链脲佐菌素(STZ)诱导的2型糖尿病模型(T2DM)小鼠,研究聚马酚的降血糖和抗2型糖尿病活性。
聚马酚含量最高,对α-葡萄糖苷酶(IC50值为6.03 mg/L)和α-淀粉酶(IC50值为19.29 mg/L)分别具有竞争性抑制和混合型抑制的最强活性。麦芽糖和淀粉负荷试验表明,与正常组(分别为11.37和12.37 mg/dL)相比,聚马酚在负荷30分钟后显著降低餐后血糖(分别为9.12和8.12 mg/dL)。聚马酚可使胰岛细胞恢复活力,表现为胰岛质量增加,从而有助于恢复胰岛素水平,进而改善STZ诱导的糖尿病小鼠的葡萄糖代谢。在T2DM小鼠中,聚马酚治疗可提高与葡萄糖代谢稳态密切相关的主要短链脂肪酸(丙酸、丁酸和戊酸)的丰度。
我们的研究结果表明,聚马酚可作为一种食品补充剂用于治疗高血糖和糖尿病。