Amelioration of High-Insulin-Induced Skeletal Muscle Cell Insulin Resistance by Resveratrol Is Linked to Activation of AMPK and Restoration of GLUT4 Translocation.
Filip VlavcheskiDanja J Den HartoghAdria GiaccaEvangelia TsianiPublished in: Nutrients (2020)
Insulin resistance, the hallmark of type 2 diabetes mellitus (T2DM), is linked to hyperinsulinemia, which develops to counterbalance initial peripheral hormone resistance. Studies indicate that chronically elevated levels of insulin lead to skeletal muscle insulin resistance by deregulating steps within the insulin signaling cascade. The polyphenol resveratrol (RSV) has been shown to have antidiabetic properties in vitro and in vivo. In the present study, we examined the effect of RSV on high insulin (HI)-induced insulin resistance in skeletal muscle cells in vitro and investigated the mechanisms involved. Parental and GLUT4myc-overexpressing L6 rat skeletal muscle cells were used. [3H]2-deoxyglucose (2DG) uptake was measured, and total and phosphorylated levels of specific proteins were examined by immunoblotting. Exposure of L6 cells to HI levels (100 nM) for 24 h decreased the acute-insulin-stimulated 2DG uptake, indicating insulin resistance. HI increased ser307 and ser636/639 phosphorylation of IRS-1 (to 184% ± 12% and 225% ± 28.9% of control, with p < 0.001 and p < 0.01, respectively) and increased the phosphorylation levels of mTOR (174% ± 6.7% of control, p < 0.01) and p70 S6K (228% ± 33.5% of control, p < 0.01). Treatment with RSV abolished these HI-induced responses. Furthermore, RSV increased the activation of AMPK and restored the insulin-mediated increase in plasma membrane GLUT4 glucose transporter levels. These data suggest that RSV has a potential to counteract the HI-induced muscle insulin resistance.
Keyphrases
- insulin resistance
- skeletal muscle
- type diabetes
- glycemic control
- high fat diet
- induced apoptosis
- polycystic ovary syndrome
- high glucose
- adipose tissue
- diabetic rats
- high fat diet induced
- metabolic syndrome
- cell cycle arrest
- oxidative stress
- drug induced
- blood glucose
- respiratory syncytial virus
- signaling pathway
- single cell
- blood pressure
- endoplasmic reticulum stress
- protein kinase
- cell death
- respiratory tract
- liver failure
- weight loss
- high resolution
- endothelial cells
- transcription factor
- atomic force microscopy
- risk assessment
- pi k akt