Insulin Sensitivity-Enhancing Activity of Phlorizin Is Associated with Lipopolysaccharide Decrease and Gut Microbiota Changes in Obese and Type 2 Diabetes (db/db) Mice - PubMed (original) (raw)
. 2016 Oct 12;64(40):7502-7511.
doi: 10.1021/acs.jafc.6b03474. Epub 2016 Sep 27.
Affiliations
- PMID: 27635781
- DOI: 10.1021/acs.jafc.6b03474
Insulin Sensitivity-Enhancing Activity of Phlorizin Is Associated with Lipopolysaccharide Decrease and Gut Microbiota Changes in Obese and Type 2 Diabetes (db/db) Mice
Xueran Mei et al. J Agric Food Chem. 2016.
Abstract
Phlorizin exists in a number of fruits and foods and exhibits many bioactivities. The mechanism of its antidiabetic effect has been known as it can competitively inhibit sodium-glucose symporters (SGLTs). However, phlorizin has a wide range of two-phase metabolism in systemic circulation and shows poor oral bioavailability. An alternative mechanism may involve gut microbiota in intestine. Sixteen obese mice with type 2 diabetes (db/db) and eight age-matched control mice (db/+) were divided into three groups: diabetic group treated with phlorizin (DMT group), vehicle-treated diabetic group (DM group), and normal control group (CC group). Phlorizin was given in normal saline solution by intragastric administration for 10 weeks. After the last treatment course, body weight, energy intake, serum lipopolysaccharides (LPS), insulin resistance, and fecal short-chain fatty acids (SCFAs) were compared. 16S rRNA gene denaturing gradient gel electrophoresis (DGGE) and quantitative PCR were used to determine the changes in microbiome composition. Coadministration of phlorizin significantly prevented metabolic syndrome by decreasing weight gain, energy intake, serum lipopolysaccharides, and insulin resistance, and the fecal level of total SCFAs was dramatically increased, especially butyric acid. DGGE and quantitative PCR demonstrated that phlorizin coadministration increased the gut microbial diversity and the growth of Akkermansia muciniphila and Prevotella. Meanwhile, the gut microbiota structure of db/db mice after phlorizin treatment was improved and approached the normal group. The mechanism of the hypoglycemic action of phlorizin is associated with LPS decrease and gut microbiota changes; briefly, it acts in the intestine to modify gut microbial community structure, resulting in lower LPS load in the host and higher SCFAs producing beneficial bacteria.
Keywords: gut microbiota; insulin resistance; lipopolysaccharides; phlorizin; short-chain fatty acids.
Similar articles
- Phlorizin ameliorates obesity-associated endotoxemia and insulin resistance in high-fat diet-fed mice by targeting the gut microbiota and intestinal barrier integrity.
Zhang XY, Chen J, Yi K, Peng L, Xie J, Gou X, Peng T, Tang L. Zhang XY, et al. Gut Microbes. 2020 Nov 9;12(1):1-18. doi: 10.1080/19490976.2020.1842990. Gut Microbes. 2020. PMID: 33222603 Free PMC article. - Metformin Is Associated With Higher Relative Abundance of Mucin-Degrading Akkermansia muciniphila and Several Short-Chain Fatty Acid-Producing Microbiota in the Gut.
de la Cuesta-Zuluaga J, Mueller NT, Corrales-Agudelo V, Velásquez-Mejía EP, Carmona JA, Abad JM, Escobar JS. de la Cuesta-Zuluaga J, et al. Diabetes Care. 2017 Jan;40(1):54-62. doi: 10.2337/dc16-1324. Epub 2016 Nov 14. Diabetes Care. 2017. PMID: 27999002 - Beneficial effects of phlorizin on diabetic nephropathy in diabetic db/db mice.
Pei F, Li BY, Zhang Z, Yu F, Li XL, Lu WD, Cai Q, Gao HQ, Shen L. Pei F, et al. J Diabetes Complications. 2014 Sep-Oct;28(5):596-603. doi: 10.1016/j.jdiacomp.2014.04.010. Epub 2014 Apr 24. J Diabetes Complications. 2014. PMID: 24927646 - Metformin: old friend, new ways of action-implication of the gut microbiome?
Rodriguez J, Hiel S, Delzenne NM. Rodriguez J, et al. Curr Opin Clin Nutr Metab Care. 2018 Jul;21(4):294-301. doi: 10.1097/MCO.0000000000000468. Curr Opin Clin Nutr Metab Care. 2018. PMID: 29634493 Review. - The role of gut microbiota in obesity, diabetes mellitus, and effect of metformin: new insights into old diseases.
Pascale A, Marchesi N, Govoni S, Coppola A, Gazzaruso C. Pascale A, et al. Curr Opin Pharmacol. 2019 Dec;49:1-5. doi: 10.1016/j.coph.2019.03.011. Epub 2019 Apr 20. Curr Opin Pharmacol. 2019. PMID: 31015106 Review.
Cited by
- Sodium-Glucose Cotransporter Inhibitors: Cellular Mechanisms Involved in the Lipid Metabolism and the Treatment of Chronic Kidney Disease Associated with Metabolic Syndrome.
Cortés-Camacho F, Zambrano-Vásquez OR, Aréchaga-Ocampo E, Castañeda-Sánchez JI, Gonzaga-Sánchez JG, Sánchez-Gloria JL, Sánchez-Lozada LG, Osorio-Alonso H. Cortés-Camacho F, et al. Antioxidants (Basel). 2024 Jun 26;13(7):768. doi: 10.3390/antiox13070768. Antioxidants (Basel). 2024. PMID: 39061837 Free PMC article. Review. - Gut microbiota in insulin resistance: a bibliometric analysis.
Tian W, Liu L, Wang R, Quan Y, Tang B, Yu D, Zhang L, Hua H, Zhao J. Tian W, et al. J Diabetes Metab Disord. 2024 Feb 14;23(1):173-188. doi: 10.1007/s40200-023-01342-x. eCollection 2024 Jun. J Diabetes Metab Disord. 2024. PMID: 38932838 Review. - The protective role of phlorizin against lipopolysaccharide-induced acute orchitis in mice associated with changes in gut microbiota composition.
Guo Q, Li TF, Huang J, Li JC, Zhang ZC, Qu YL. Guo Q, et al. Front Vet Sci. 2024 May 23;11:1340591. doi: 10.3389/fvets.2024.1340591. eCollection 2024. Front Vet Sci. 2024. PMID: 38846786 Free PMC article. - Local and Systemic Effects of Bioactive Food Ingredients: Is There a Role for Functional Foods to Prime the Gut for Resilience?
Jacquier EF, van de Wouw M, Nekrasov E, Contractor N, Kassis A, Marcu D. Jacquier EF, et al. Foods. 2024 Feb 28;13(5):739. doi: 10.3390/foods13050739. Foods. 2024. PMID: 38472851 Free PMC article. Review. - Phlorizin, an Important Glucoside: Research Progress on Its Biological Activity and Mechanism.
Ni T, Zhang S, Rao J, Zhao J, Huang H, Liu Y, Ding Y, Liu Y, Ma Y, Zhang S, Gao Y, Shen L, Ding C, Sun Y. Ni T, et al. Molecules. 2024 Feb 5;29(3):741. doi: 10.3390/molecules29030741. Molecules. 2024. PMID: 38338482 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Miscellaneous