Scopoletin Supplementation Ameliorates Steatosis and Inflammation in Diabetic Mice.
Ra-Yeong ChoiJu Ri HamMi-Kyung LeeHyun Wook ChoMyung-Sook ChoiSeok-Kyu ParkJin LeeMyung-Joo KimKwon-Il SeoMi-Kyung LeePublished in: Phytotherapy research : PTR (2017)
Scopoletin is a bioactive component in many edible plants and fruits. This study investigated the effects of scopoletin on hepatic steatosis and inflammation in a high-fat diet fed type 1 diabetic mice by comparison with metformin. Scopoletin (0.01%, w/w) or metformin (0.5%, w/w) was provided with a high-fat diet to streptozotocin-induced diabetic mice for 11 weeks. Both scopoletin and metformin lowered blood glucose and HbA1c , serum ALT, TNF-α and IL-6 levels, glucose intolerance, and hepatic lipid accumulation compared with the diabetic control group. Scopoletin or metformin down-regulated hepatic gene expression of triglyceride (Pparg, Plpp2, and Dgat2) and cholesterol (Hmgcr) synthesis as well as inflammation (Tlr4, Myd88, Nfkb1, Tnfa, and Il6), while it up-regulated Cyp7a1 gene. Hepatic PPARγ and DGAT2 protein levels were also down-regulated in scopoletin or metformin group compared with the control group. Scopoletin or metformin also inhibited hepatic fatty acid synthase and phosphatidate phosphohydrolase activities. These results suggest that scopoletin protects against diabetes-induced steatosis and inflammation by inhibiting lipid biosynthesis and TLR4-MyD88 pathways. Copyright © 2017 John Wiley & Sons, Ltd.
Keyphrases
- high fat diet
- insulin resistance
- blood glucose
- oxidative stress
- adipose tissue
- gene expression
- toll like receptor
- diabetic rats
- fatty acid
- type diabetes
- glycemic control
- immune response
- transcription factor
- cardiovascular disease
- metabolic syndrome
- rheumatoid arthritis
- signaling pathway
- blood pressure
- genome wide
- dna methylation
- nuclear factor
- mouse model
- preterm birth
- cell wall
- binding protein
- genome wide identification
- atomic force microscopy