2019
DOI: 10.29219/fnr.v63.1598
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A novel polysaccharide from Lentinus edodes mycelia protects MIN6 cells against high glucose-induced damage via the MAPKs and Nrf2 pathways

Abstract: Background Diabetes mellitus is one of the most widespread diseases in the world, high glucose can damage islet cells, it is important to discover new natural products to inhibit high glucose damage. The protective effects and mechanisms of a novel Lentinus edodes mycelia polysaccharide (LMP) against damage induced by high glucose in MIN6 cells were explored. Methods Cell viability, malondialdehyde (MDA) inhibition, lactate dehydrogenase (LDH) release and the activity o… Show more

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Cited by 21 publications
(17 citation statements)
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“…Hoechst 33258 is a fluorescent dye that can enter the cell membrane and has low toxicity, it can stain cells by binding to DNA. The degree of apoptosis is indicated by the intensity of blue fluorescence [35,36] . To detect the effect of MGO on the apoptosis of HEK293 cells, Hoechst 33258 fluorescent staining assay was carried out.…”
Section: Resultsmentioning
confidence: 99%
“…Hoechst 33258 is a fluorescent dye that can enter the cell membrane and has low toxicity, it can stain cells by binding to DNA. The degree of apoptosis is indicated by the intensity of blue fluorescence [35,36] . To detect the effect of MGO on the apoptosis of HEK293 cells, Hoechst 33258 fluorescent staining assay was carried out.…”
Section: Resultsmentioning
confidence: 99%
“…While the specific molecular basis for DCM remains to be fully clarified, it is thought to develop in part through an inflammatory mechanism (29,30). The hyperglycemic state that exists in T2DM patients can drive the increased production of intracellular ROS, thereby driving tissue injury and inflammation (31,32). Inflammatory cardiomyocyte signaling is associated with the overproduction of both cytosolic and mitochondrial ROS (33,34).…”
Section: Discussionmentioning
confidence: 99%
“…The plates with B. cereus and S. typhimurium were incubated at 37°C for 24 h. The suspension in each well was removed and the microtiter wells were washed for four times with PBS to remove non-adherent cells. Biofilms were stained with MTT solution (prepared with the corresponding medium) and incubated in dark for 3 h at 37°C (34,35). Dimethyl sulfoxide (DMSO) was used to rinse after removal of MTT solution.…”
Section: Inhibition Activitymentioning
confidence: 99%