TY - JOUR
T1 - Combination of scutellaria baicalensis and metformin ameliorates diet-induced metabolic dysregulation in mice via the gut-liver-brain axis
AU - Ansari, Abu Zar
AU - Bose, Shambhunath
AU - Lim, Soo Kyoung
AU - Wang, Jing Hua
AU - Choi, Young Hee
AU - Kim, Hojun
N1 - Publisher Copyright:
© 2020 World Scientific Publishing Company
PY - 2020
Y1 - 2020
N2 - 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 PPARγ, 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.
AB - 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 PPARγ, 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.
KW - Metabolic Dysregulation
KW - Metformin
KW - Microbiota
KW - Scutellaria baicalensis
UR - http://www.scopus.com/inward/record.url?scp=85091866570&partnerID=8YFLogxK
U2 - 10.1142/S0192415X2050069X
DO - 10.1142/S0192415X2050069X
M3 - Article
C2 - 32907360
AN - SCOPUS:85091866570
SN - 0192-415X
VL - 48
SP - 1409
EP - 1433
JO - American Journal of Chinese Medicine
JF - American Journal of Chinese Medicine
IS - 6
ER -