Key result
Aurantio-obtusin improved adiposity, insulin resistance, and dyslipidemia in high-fat diet-induced obese mice by regulating insulin signaling, lipid metabolism genes, and inflammatory cytokines.
Why the study?
Does Aurantio-obtusin improve obesity and insulin resistance in high-fat diet-induced obese mice?
Does Aurantio-obtusin improve obesity and insulin resistance in high-fat diet-induced obese mice?
Aurantio-obtusin may improve adiposity, insulin resistance, and dyslipidemia by regulating insulin signaling and lipid metabolism pathways in a preclinical model.
Answers are grounded in this paper and cite their sources.
Should not change practice; hypothesis-generating for aurantio-obtusin in metabolic disease.
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.
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Guo et al. (2020) studied Obesity and insulin resistance. Aurantio-obtusin (AUR) vs. High-fat diet (HFD) control group was evaluated on Improvement in obesity, insulin resistance, and dyslipidemia. Aurantio-obtusin improved adiposity, insulin resistance, and dyslipidemia in high-fat diet-induced obese mice by regulating insulin signaling, lipid metabolism genes, and inflammatory cytokines.
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