School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, PR China; National Engineering Research Center of Seafood, Dalian 116034, PR China; National & Local Joint Engineering Laboratory for Marine Bioactive Polysaccharide Development and Application, Dalian Polytechnic University, Dalian 116034, PR China.
School of Food Science and Technology, Dalian Polytechnic University, Dalian 116034, PR China; National Engineering Research Center of Seafood, Dalian 116034, PR China; National & Local Joint Engineering Laboratory for Marine Bioactive Polysaccharide Development and Application, Dalian Polytechnic University, Dalian 116034, PR China; Department of Food Science, University of Massachusetts, Amherst, MA 01003, USA.
Int J Biol Macromol. 2019 Oct 1;138:49-56. doi: 10.1016/j.ijbiomac.2019.07.072. Epub 2019 Jul 10.
Polysaccharides with different structures have been reported to regulate iron uptake in opposite direction. The present study investigated the interaction between a sulfated polysaccharide (AGSP) from marine shellfishes and Fe(III)/Fe(II) in order to reveal the mechanism for the effect of AGSP on iron bioavailability. The Fe(III) chelating activity and resulting Fe(III)-chelates of AGSP and its desulfated derivative (dS-AGSP) were studied, their ferric reducing activity and Fe(II) chelating activity were compared, and their inhibition effects on the Fe absorption were evaluated by using Caco-2 cell models treated with Fe(III) and Fe(II). As indicated by the results, polysaccharides could chelate Fe(III) with the sulfate and carboxyl groups via FeO bond along with conformation change, resulting in unstable particles. Both AGSP and dS-AGSP inhibited the iron uptake in a dose-dependent manner. Notably, the chelating property of polysaccharides showed a negative correlation with the iron bioavailability while their reducing capability demonstrated a positive correlation. Moreover, sulfate substitution enhanced the chelating and reducing capabilities so to regulate the effects of AGSP on Fe absorption in contradictory ways. Thus, the present study elucidated the mechanism of the influence of AGSP on bioavailability of non-heme iron.
具有不同结构的多糖被报道以相反的方向调节铁的摄取。本研究旨在探讨海洋贝类来源的硫酸多糖(AGSP)与 Fe(III)/Fe(II)之间的相互作用,以揭示 AGSP 对铁生物利用度影响的作用机制。研究了 AGSP 及其去硫酸衍生物(dS-AGSP)的 Fe(III)螯合活性及其形成的 Fe(III)-螯合物,比较了它们的铁还原活性和 Fe(II)螯合活性,并通过用 Caco-2 细胞模型处理 Fe(III)和 Fe(II)来评估它们对铁吸收的抑制作用。结果表明,多糖可通过 FeO 键与硫酸盐和羧基结合,从而改变其构象,对 Fe(III)进行螯合,导致不稳定的颗粒。AGSP 和 dS-AGSP 均以剂量依赖的方式抑制铁的摄取。值得注意的是,多糖的螯合特性与铁的生物利用度呈负相关,而其还原能力呈正相关。此外,硫酸基取代增强了多糖的螯合和还原能力,从而以相反的方式调节 AGSP 对 Fe 吸收的影响。因此,本研究阐明了 AGSP 对非血红素铁生物利用度影响的作用机制。