Selenium-containing polysaccharide from Spirulina platensis alleviates Cd-induced toxicity in mice by inhibiting liver inflammation mediated by gut microbiota

被引:14
作者
Zhou, Ning [1 ]
Long, Hairong [2 ]
Yu, Lian [1 ]
Xia, Xianghua [2 ]
Zhu, Zhenjun [3 ]
Liu, Xiaoling [1 ]
机构
[1] Guangxi Univ, Coll Light Ind & Food Engn, Nanning, Peoples R China
[2] Guangxi Bot Garden Med Plants, Nanning, Peoples R China
[3] Jinan Univ, Coll Sci & Engn, Dept Food Sci & Engn, Guangzhou, Peoples R China
来源
FRONTIERS IN NUTRITION | 2022年 / 9卷
关键词
gut microbiota; liver inflammation; Cd-induced toxicity; selenium polysaccharide; Spirulina platensis; OXIDATIVE STRESS; BARRIER FUNCTION; CADMIUM; EXPOSURE;
D O I
10.3389/fnut.2022.950062
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Selenium-containing polysaccharide from Spirulina platensis (Se-SPP) has been demonstrated to help in inhibiting cadmium-induced injury in mice, but the underlying mechanism has not been determined. This study aimed to investigate the beneficial effects of Se-SPP on alleviating Cd-induced toxicity in mice by targeting liver inflammatory and gut microbiota. Se-SPP supplementation for 28 days in Cd-induced toxic mice significantly mitigated liver pathological damage and inflammation, which was correlated to the upregulation of antioxidant enzyme activity. Furthermore, Se-SPP effectively restored Cd-induced disruption of the intestinal barrier compared to model group, as indicated by the depletion of Muribaculaceae and the enrichment of Ruminococcaceae. Spearman's correlation analysis revealed that the Se-SPP-altered microbes were highly correlated with inflammation-related indexes in Cd-induced toxic mice. Noteworthily, the modulation of Se-SPP on the Ruminococcaceae population contributed to the improvement of Cd-induced inflammation-related diseases by downregulating the tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma) in the liver. These findings suggested that Se-SPP may act as prebiotics for ameliorating Cd-induced toxicity in mice by inhibiting liver inflammation mediated by gut microbiota, and target-specific microbiota of Cd-induced inflammation-related diseases deserve further attention.
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页数:13
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