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中国圆田螺多糖的初步表征及其潜在的保肝作用。

Preliminary characterization and potential hepatoprotective effect of polysaccharides from Cipangopaludina chinensis.

机构信息

College of Life Science and Chemical Engineering, Huaiyin Institute of Technology, Huaian 223003, Jiangsu, PR China.

出版信息

Food Chem Toxicol. 2013 Sep;59:18-25. doi: 10.1016/j.fct.2013.05.036. Epub 2013 May 31.

Abstract

In the present study, we investigated the preliminary characterization, in vitro antioxidant and in vivo heptoprotective activities of polysaccharides from Cipangopaludina chinensis (CCPS). The results of chemical and gas chromatography analysis indicated that CCPS was mostly composed of glucose with high contents of uronic acid and sulfate. For antioxidant activities in vitro, CCPS showed medium lipid peroxidation inhibition effect and high Fe²⁺ chelating and hydroxyl radical scavenging activities. For hepatoprotective activity in vivo, the administration of CCPS significantly decreased the serum levels of alanine aminotransferase and aspartate aminotransferase, inhibited the formation of malondialdehyde in liver and tumor necrosis factor-alpha (TNF-α) in serum and restored the liver activities of superoxide dismutase, glutathione peroxidase in BCG/LPS-induced immunological liver injury mice. The results suggested that CCPS had a significant protective effect against BCG/LPS-induced immunological liver injury. The hepatoprotective effect of CSPS might be partly due to its immunoregulatory effect by inhibiting TNF-α production and antioxidant activities to protect biological systems against the oxidative stress, which were dependent on the chemical and structural properties of CCPS. Further work on the structure of CCPS is in progress.

摘要

在本研究中,我们研究了中国圆田螺多糖(CCPS)的初步特性、体外抗氧化活性和体内保肝活性。化学和气相色谱分析的结果表明,CCPS 主要由葡萄糖组成,含有较高的糖醛酸和硫酸盐。体外抗氧化活性结果表明,CCPS 具有中等的脂质过氧化抑制作用,以及较高的 Fe²⁺螯合和羟基自由基清除活性。体内保肝活性结果表明,CCPS 给药可显著降低丙氨酸氨基转移酶和天冬氨酸氨基转移酶的血清水平,抑制肝组织丙二醛和血清肿瘤坏死因子-α(TNF-α)的形成,并恢复 BCG/LPS 诱导的免疫性肝损伤小鼠肝组织中超氧化物歧化酶和谷胱甘肽过氧化物酶的活性。结果表明,CCPS 对 BCG/LPS 诱导的免疫性肝损伤具有显著的保护作用。CSPS 的保肝作用可能部分归因于其通过抑制 TNF-α产生和抗氧化活性来调节免疫的作用,从而保护生物系统免受氧化应激的影响,这与 CCPS 的化学和结构特性有关。目前正在对 CCPS 的结构进行进一步研究。

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