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Aurantio‐obtusin improves obesity and insulin resistance induced by high‐fat diet in obese mice
- Source :
- Phytotherapy Research. 35:346-360
- Publication Year :
- 2020
- Publisher :
- Wiley, 2020.
-
Abstract
- Aurantio-obtusin (AUR) is the main bioactive compound among the anthraquinones, from Cassia seed extract. This study was conducted to identify whether AUR could improve obesity and insulin resistance, induced by a high-fat diet in obese mice. Mice were fed a high-fat diet for 6 weeks and were then assigned to the high-fat diet (HFD) control group, the AUR 5 mg/kg group, or the AUR 10 mg/kg group. AUR improves glucose by activating the expression of PI3K, Akt and GLUT4, GLUT2. AUR altered the expression levels of several lipid metabolism-related and adipokine genes. AUR decreased the mRNA expression of PPAR-γ, FAS and increased the mRNA expression of PPAR-α in liver. AUR lowered SREBP-1c, FAS, SCD-1, inflammatory cytokines, and increased the expression of PPAR-γ, PPAR-α, CPT-1, and adiponectin in white adipose tissue (WAT). AUR docking with the insulin receptor showed that the residues of the insulin receptor, ectodomain, were the same as those around the emodin. The effect of AUR may be elicited by regulating the activity of the insulin signaling pathway, expression of lipid metabolism-related genes, and expression of inflammatory cytokine markers to improve adiposity, insulin resistance, and dyslipidemia.
- Subjects :
- Male
medicine.medical_specialty
Adipose Tissue, White
Cassia
Mice, Obese
Adipokine
Anthraquinones
White adipose tissue
Diet, High-Fat
Mice
03 medical and health sciences
0302 clinical medicine
Insulin resistance
Internal medicine
medicine
Animals
Obesity
Protein kinase B
Pharmacology
0303 health sciences
biology
Adiponectin
business.industry
030302 biochemistry & molecular biology
Lipid Metabolism
medicine.disease
Receptor, Insulin
Mice, Inbred C57BL
PPAR gamma
Insulin receptor
Endocrinology
Liver
030220 oncology & carcinogenesis
Seeds
biology.protein
Insulin Resistance
Sterol Regulatory Element Binding Protein 1
business
Dyslipidemia
GLUT4
Signal Transduction
Subjects
Details
- ISSN :
- 10991573 and 0951418X
- Volume :
- 35
- Database :
- OpenAIRE
- Journal :
- Phytotherapy Research
- Accession number :
- edsair.doi.dedup.....b5475a4545d081b079591fc0e83bfcee