2021
DOI: 10.1016/j.biopha.2020.110966
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Characterization of local gut microbiome and intestinal transcriptome responses to rosiglitazone treatment in diabetic db/db mice

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Cited by 13 publications
(13 citation statements)
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“…Those modifications were reversible after starting a normal diet or one week treatment with rosiglitazone [ 78 ]. In a recently published study, diabetic B6.BKS(D)-Lepr db /J (db/db) mice that received rosiglitazone for 8 weeks developed changes in segment-specific host gene expression, without modifications of gut bacterial composition [ 79 ]. These data suggest a possible involvement of the TZDs on microbiota, but human studies regarding the impact of the drug on the microbiota in T2DM have not been reported.…”
Section: Microbiota and Therapy For Diabetes Mellitusmentioning
confidence: 99%
“…Those modifications were reversible after starting a normal diet or one week treatment with rosiglitazone [ 78 ]. In a recently published study, diabetic B6.BKS(D)-Lepr db /J (db/db) mice that received rosiglitazone for 8 weeks developed changes in segment-specific host gene expression, without modifications of gut bacterial composition [ 79 ]. These data suggest a possible involvement of the TZDs on microbiota, but human studies regarding the impact of the drug on the microbiota in T2DM have not been reported.…”
Section: Microbiota and Therapy For Diabetes Mellitusmentioning
confidence: 99%
“…In addition to the above-mentioned antidiabetic drugs, the influence of sulfonylurea, peroxisome proliferative activated receptor (PPARG) agonists and insulin on microbiota composition and the consequent metabolic benefits has also been emphasized ( Huo et al., 2015 ; Zhang F. et al., 2019 ; Madsen et al., 2021 ). Insulin increased the abundance of Fusobacterium , which up-regulated the genes involved in triglyceride and arachidonic acid metabolism ( Zhang F. et al., 2019 ).…”
Section: Interaction Between Gut Microbiota and Antidiabetic Drugsmentioning
confidence: 99%
“…Recently, Madsen et al. revealed that rosiglitazone, a PPARG agonist, improved glucose homeostasis without influencing local gut microbiome in diabetic db/db mice by using full-length bacterial 16S rRNA sequencing ( Madsen et al., 2021 ).…”
Section: Interaction Between Gut Microbiota and Antidiabetic Drugsmentioning
confidence: 99%
“…In diabetic db/db mice, rosiglitazone treatment significantly improved insulin sensitivity and glucose homeostasis without altering gut bacterial composition. 87 A global gene expression analysis in rosiglitazone-treated db/db mice showed substantial changes in colon and ileum, with no change in duodenum. Rosiglitazone treatment stimulated fatty acid metabolism by regulating the gene markers of intestinal fatty uptake, transport and disposal in the colon and ileum.…”
Section: Thiazolidinediones (Tzds)mentioning
confidence: 99%
“…These effects were consistent with the fact that PPAR-γ being abundantly expressed in colonic epithelial cells. 87 Another study found that Danshensu Bingpian Zhi (DBZ), a unique PPAR-γ partial agonist, prevented HFD-induced obesity and insulin resistance through modulating gut microbiota dysbiosis. 88 DBZ treatment restored intestinal barrier integrity and reversed gut dysbiosis by increasing the ratio of Bacteroidetes to Firmicutes, the relative abundance of Akkermansia, and reducing the level of HFD-induced pernicious bacteria (such as Helicobacter marmotae, Odoribacter, and Anaerotruncus).…”
Section: Thiazolidinediones (Tzds)mentioning
confidence: 99%