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Cited 30 time in webofscience Cited 33 time in scopus
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Lactobacillus Sps in Reducing the Risk of Diabetes in High-Fat Diet-Induced Diabetic Mice by Modulating the Gut Microbiome and Inhibiting Key Digestive Enzymes Associated with Diabetesopen access

Authors
Gulnaz, AneelaNadeem, JawadHan, Jong-HunLew, Lee-ChingSon, Jae-DongPark, Yong-HaRather, Irfan A.Hor, Yan-Yan
Issue Date
Apr-2021
Publisher
MDPI
Keywords
Type 2 diabetes; gut-microbiome; HFD-diet; Lactobacillus; probiotics; α -glucosidase; α -amylase; 16S RNA gene; mice; fecal samples
Citation
BIOLOGY-BASEL, v.10, no.4
Indexed
SCIE
SCOPUS
Journal Title
BIOLOGY-BASEL
Volume
10
Number
4
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/72768
DOI
10.3390/biology10040348
ISSN
2079-7737
Abstract
Simple Summary Type 2 diabetes (T2D) is increasingly spreading across the globe. The disease is linked to a disruption of gut microbiome. Probiotics are essential gut microbiota modulators proven to restore microbiota changes, thereby conferring health to its host. This study aimed to use probiotics (lactobacilli) and their metabolites as natural anti-diabetic therapy through the modulation of gut microbiota and inhibit diabetes-causing enzymes. Lactobacillus-treated high-fat diet mice showed lower blood glucose levels and body weight. Interestingly, our study also proved that the lactobacilli altered gut microbiota composition by suppressing opportunistic bacteria that are highly associated with metabolic diseases. Our findings substantiate the use of probiotics as natural anti-diabetic therapeutics. Obesity caused by a high-fat diet (HFD) affects gut microbiota linked to the risk of type-2 diabetes (T2D). This study evaluates live cells and ethanolic extract (SEL) of Lactobacillus sakei Probio65 and Lactobacillus plantarum Probio-093 as natural anti-diabetic compounds. In-vitro anti-diabetic effects were determined based on the inhibition of alpha-glucosidase and alpha-amylase enzymes. The SEL of Probio65 and Probio-093 significantly retarded alpha-glucosidase and alpha-amylase enzymes (p < 0.05). Live Probio65 and Probio-093 inhibited alpha-glucosidase and alpha-amylase, respectively (p < 0.05). In mice fed with a 45% kcal high-fat diet (HFD), the SEL and live cells of both strains reduced body weight significantly compared to HFD control (p < 0.05). Probio-093 also improved blood glucose level compared to control (p < 0.05). The gut microbiota modulatory effects of lactobacilli on HFD-induced diabetic mice were analyzed with qPCR method. The SEL and live cells of both strains reduced phyla Deferribacteres compared to HFD control (p < 0.05). The SEL and live cells of Probio-093 promoted more Actinobacteria (phyla), Bifidobacterium, and Prevotella (genus) compared to control (p < 0.05). Both strains exerted metabolic-modulatory effects, with strain Probio-093 showing more prominent alteration in gut microbiota, substantiating the role of probiotics in gut microbiome modulations and anti-diabetic effect. Both lactobacilli are potential candidates to lessen obesity-linked T2D.
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