2017
DOI: 10.1016/j.jff.2017.09.032
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Ganoderma lucidum polysaccharides improve insulin sensitivity by regulating inflammatory cytokines and gut microbiota composition in mice

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Cited by 79 publications
(30 citation statements)
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“…Hepatocyte injury and inflammation could be promoted by hepatic insulin resistance [16,42]. It has been reported that different sources of polysaccharides (such as Ganoderma lucidum) could improve insulin resistance by regulating gut microbiota composition and inflammatory cytokines [43]. In the present study, different polysaccharides were screened, and the insulin sensitivity was improved by polysaccharides from S. miltiorrhiza Bunge, which was the outstanding performer among the tested polysaccharides.…”
Section: Discussionmentioning
confidence: 76%
See 1 more Smart Citation
“…Hepatocyte injury and inflammation could be promoted by hepatic insulin resistance [16,42]. It has been reported that different sources of polysaccharides (such as Ganoderma lucidum) could improve insulin resistance by regulating gut microbiota composition and inflammatory cytokines [43]. In the present study, different polysaccharides were screened, and the insulin sensitivity was improved by polysaccharides from S. miltiorrhiza Bunge, which was the outstanding performer among the tested polysaccharides.…”
Section: Discussionmentioning
confidence: 76%
“…The function of the probiotic LB was enhanced by S. miltiorrhiza Bunge polysaccharide. In previous research, polysaccharides have been used to reduce IL-6, IL-1β, and TNF-α concentrations in plasma [43]. TNF-α expression and hepatic inflammation can be reduced by L. rhamnosus and other probiotics [44].…”
Section: Discussionmentioning
confidence: 99%
“…Subsequently, blood glucose levels were measured using AccuCheck Active glucometer with test strips (Roche Diagnostics, Mannheim, Germany). The area under the curve (AUC) for glucose was calculated, according to the previously described method …”
Section: Methodsmentioning
confidence: 99%
“…The blood samples were centrifuged at 7000 × g for 10 min at 4°C. Serum was immediately collected, frozen, and stored at -80°C until analysis [ 28 ]. Tissues were snap frozen by liquid nitrogen and preserved in the -80°C refrigerator for further analysis.…”
Section: Methodsmentioning
confidence: 99%