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浒苔多糖-Fe/Zn 复合物的结构表征及抗炎作用。

Structural characterization and anti-inflammatory effects of Enteromorpha prolifera polysaccharide-Fe/Zn complexes.

机构信息

Tianjin Institute of Industrial Biotechnology, Chinese Academy of Sciences, Tianjin 300308, China.

Qingdao Seawin Biotech Group Co., LTD, Qingdao 266071, China.

出版信息

Int J Biol Macromol. 2023 Dec 31;253(Pt 6):127166. doi: 10.1016/j.ijbiomac.2023.127166. Epub 2023 Sep 29.

Abstract

The structure of polysaccharide has a great influence on its biological functions, and the chelation with metal ions is an effective way to change polysaccharide structural configuration. Herein, the structure of Enteromorpha prolifera polysaccharide (EP)-Fe/Zn complexes were characterized and the results showed that the iron (III) existed in form of β-FeOOH in EP-Fe (III) complex and the zinc (II) existed in form of C-O-Zn in EP-Zn (II) complex. Besides, the chelation with iron (III) or zinc (II) completely changed the apparent forms, and improved the thermal stability of EP. Furthermore, the anti-inflammatory activities of EP, EP-Fe and EP-Zn were proved by a lipopolysaccharide (LPS)-induced RAW264.7 macrophages model. The results showed that EP, EP-Fe (III) and EP-Zn (II) could decrease the mitochondrial membrane potential and the secretion of NO and cytokines induced by LPS. One of the anti-inflammatory mechanisms of EP, EP-Fe (III) and EP-Zn (II) was that they could inhibit mitogen-activated protein kinase (MAPK) signaling pathway via increasing its inhibitor content in cells. Collectively, the research suggested that the chelation with iron (III) or zinc (II) could change the structure and improve the anti-inflammatory activities of EP.

摘要

多糖的结构对其生物功能有很大影响,而与金属离子螯合是改变多糖结构构象的有效方法。本文中,对孔石莼多糖(EP)-Fe/Zn 复合物的结构进行了表征,结果表明 EP-Fe(III)复合物中的铁(III)以β-FeOOH 的形式存在,而 EP-Zn(II)复合物中的锌(II)以 C-O-Zn 的形式存在。此外,与铁(III)或锌(II)的螯合完全改变了 EP 的表观形式,提高了其热稳定性。此外,通过脂多糖(LPS)诱导的 RAW264.7 巨噬细胞模型证实了 EP、EP-Fe 和 EP-Zn 的抗炎活性。结果表明,EP、EP-Fe(III)和 EP-Zn(II)可以降低 LPS 诱导的线粒体膜电位和 NO 及细胞因子的分泌。EP、EP-Fe(III)和 EP-Zn(II)的抗炎机制之一是通过增加细胞内其抑制剂的含量来抑制丝裂原活化蛋白激酶(MAPK)信号通路。综上所述,研究表明,与铁(III)或锌(II)的螯合可以改变 EP 的结构并提高其抗炎活性。

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