4.7 Article

Combination of Scutellaria baicalensis and Metformin Ameliorates Diet-Induced Metabolic Dysregulation in Mice via the Gut-Liver-Brain Axis

期刊

AMERICAN JOURNAL OF CHINESE MEDICINE
卷 48, 期 6, 页码 1409-1433

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WORLD SCIENTIFIC PUBL CO PTE LTD
DOI: 10.1142/S0192415X2050069X

关键词

Scutellaria baicalensis; Metformin; Metabolic Dysregulation; Microbiota

资金

  1. Convergence of Conventional Medicine and Traditional Medicine Korean Medicine R&D - Ministry of Health and Welfare through the Korean Health Industry Development Institute [HI14C0558]

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Scutellaria baicalensis (SB), a herbal medicine, is commonly used to treat metabolic diseases, while Metformin (MF) is a widely used drug for type 2 diabetes. The purpose of this study was to investigate whether co-treatment of SB with MF could produce a potential therapeutic effect on high-fat and high-fructose diet (HFFD)-induced metabolic dysregulation. First, we optimized the dose of SB (100, 200, 400, and 800 mg/kg) with MF (200 mg/kg) in HFFD-induced C57BL6J mice. Next, the optimized dose of SB (400 mg/kg) was co-administered with MF (50, 100, and 200 mg/kg) in a similar animal model to find the effective combinations of SB and MF. Metabolic markers were determined in serum and tissues using different assays, histology, gene expression, and gut microbial population. The SB and MF co-treatment significantly decreased the body, liver, and VAT weights. The outcome of OGTT was improved, and the fasting insulin, HbA1c, TG, TC, LDL-c, AST, and ALT were decreased, while HDL-c was significantly increased. Histological analyses revealed maintained the integrity of liver, adipose tissue, and intestine prevented lipid accumulation in the liver and intestine and combated neuronal damage in the brain. Importantly, controlled the expression of PPAR gamma, and IL-6 genes in the liver, and expression of BDNF, Glut1, Glut3, and Glut4 genes in the brain. Treatment-specific gut microbial segregation was observed in the PCA chart. Our findings indicate that SB and MF co-treatment is an effective therapeutic approach for HFFD-induced metabolic dysregulation which is operated through the gut-liver-brain axis.

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