Related Experiment Video
Updated: Jul 19, 2025

Mechanism of Kemeng Fang's Inhibition of Podocyte Apoptosis in Rats with Membranous Nephropathy through the PI3K/AKT Signaling Pathway
Published on: August 23, 2024
Antidiabetic activity of eupafolin through peroxisome proliferator-activated receptor-gamma and PI3K/Akt signaling in
1Department of General Medicine, Jiangxi Provincial People's Hospital, The First Affiliated Hospital of Nanchang Medical College, Nanchang City, Jiangxi Province, China.
Abstract:
Eupafolin is a phyto compound of flavone that exerts anti-inflammatory, antioxidant, and antiproliferative properties. The main purpose of this study is to examine the antidiabetic effect of eupafolin on nicotinamide-streptozotocin (STZ)-induced Type 2 diabetes (T2D) rats. After nicotinamide (120 mg/kg) treatment, STZ (60 mg/kg) was administrated intravenously to induce T2D. Rats with fasting blood glucose (FBG) > 200 mg/dL are chosen for the study 7 days after T2D induction. The eupafolin treatment was continued for another 15 days. FBG and an oral glucose tolerance test (OGTT) were measured on the 21st day after T2D induction. The blood lipid, serum insulin, and homeostatic model assessment (HOMA-IR) were determined. In liver homogenate, oxidative stress indicators were measured. In addition, the effect of eupafolin on the expression of the proteins InsR, insulin receptor substrate (IRS)-2, GLUT4, PPARγ, and phosphatidylinositol 3-kinase (PI3K)/Akt was investigated using a western blot. As measured by OGTT and HOMA-IR, eupafolin treatment reduced FBG and insulin resistance (IR). Furthermore, when compared to diabetic rats, liver antioxidant enzymes were dramatically normalized. The level of glycogen in the liver of diabetic rats was increased by eupafolin treatment. In T2D rats, eupafolin dramatically increased the InsR, IRS-2, GLUT4, and PPARγ. Further, the eupafolin treatment activated the PI3K/Akt signaling in T2D rats. These findings imply that the antidiabetic mechanism of eupafolin may be related to the activation of the PPARγ and the PI3K/Akt signaling pathway in T2D rats. As a result, the flavonoid eupafolin could be an antidiabetic medication for T2D after a comprehensive clinical investigation.
Insights
Eupafolin, a flavonoid, effectively lowers blood glucose and insulin resistance in Type 2 Diabetes (T2D) rats. It also improves liver antioxidant function and activates key signaling pathways, suggesting potential as an antidiabetic drug.
Area of Science:
- Pharmacology and Toxicology
- Endocrinology and Metabolism
- Biochemistry
Background:
- Eupafolin is a flavone phyto-compound with known anti-inflammatory, antioxidant, and antiproliferative effects.
- Type 2 Diabetes (T2D) is a metabolic disorder characterized by insulin resistance and hyperglycemia.
- Developing novel therapeutic agents for T2D is a significant medical need.
Purpose of the Study:
- To investigate the antidiabetic effects of eupafolin in a rat model of T2D.
- To elucidate the molecular mechanisms underlying eupafolin's action in T2D.
Main Methods:
- Type 2 Diabetes was induced in rats using nicotinamide and streptozotocin (STZ).
- Eupafolin treatment was administered for 15 days to diabetic rats.
- Key metabolic parameters, insulin signaling proteins (InsR, IRS-2, GLUT4, PI3K/Akt), and liver oxidative stress markers were assessed.
Main Results:
- Eupafolin treatment significantly reduced fasting blood glucose (FBG) and improved glucose tolerance.
- Insulin resistance (IR), assessed by HOMA-IR, was markedly decreased.
- Eupafolin normalized liver antioxidant enzymes, increased liver glycogen, and upregulated InsR, IRS-2, GLUT4, and PPARγ expression.
- Activation of the PI3K/Akt signaling pathway was observed.
Conclusions:
- Eupafolin demonstrates significant antidiabetic properties in a T2D rat model.
- Its mechanism involves enhancing insulin sensitivity, improving antioxidant capacity, and activating the PPARγ and PI3K/Akt signaling pathways.
- Eupafolin shows promise as a potential therapeutic agent for Type 2 Diabetes, warranting further clinical investigation.
Related Concept Videos
Dipeptidyl Peptidase 4 Inhibitors
Insulin: The Receptor and Signaling Pathways
Glucagon-like Receptor Agonists
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
PI3K/mTOR/AKT Signaling Pathway
Oral Hypoglycemic Agents: Biguanides and Glitazones
cAMP-dependent Protein Kinase Pathways

