3,4',5-Trimethoxy- trans -stilbene ameliorates hepatic insulin resistance and oxidative stress in diabetic obese mice through insulin and Nrf2 signaling pathways.
Yi TanChunxiu ZhouLingchao MiaoXutao ZhangHaroon KhanBaojun XuWai San CheangPublished in: Food & function (2024)
Resveratrol has profound benefits against diabetes. However, whether its methylated derivative 3,4',5-trimethoxy- trans -stilbene (3,4',5-TMS) also plays a protective role in glucose metabolism is not characterized. We aimed to study the anti-diabetic effects of 3,4',5-TMS in vitro and in vivo . Insulin-resistant HepG2 cells (IR-HepG2) were induced by high glucose plus dexamethasone whilst six-week-old male C57BL/6J mice received a 60 kcal% fat diet for 14 weeks to establish an obese diabetic model. 3,4',5-TMS did not reduce the cell viability of IR-HepG2 cells at concentrations of 0.5 and 1 μM, which enhanced the capability of glycogen synthesis and glucose consumption in IR-HepG2 cells. Four-week oral administration of 3,4',5-TMS at 10 mg kg -1 day -1 ameliorated insulin sensitivity and glucose tolerance of diet-induced obese (DIO) mice. 3,4',5-TMS activated the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) pathway by inhibiting phosphorylation of insulin receptor substrate (IRS)-1 at Ser307 and increasing the protein levels of IRS-1 and IRS-2 to restore the insulin signaling pathway in diabetes. 3,4',5-TMS also upregulated the phosphorylation of glycogen synthase kinase 3 beta (GSK3β) at Ser9. 3,4',5-TMS suppressed oxidative stress by increasing the protein levels of nuclear factor erythroid 2-related factor 2 (Nrf2), heme oxygenase-1 (HO-1) and NAD(P)H : quinone oxidoreductase 1 (NQO1) and antioxidant enzyme activity. In summary, 3,4',5-TMS alleviated hepatic insulin resistance in vitro and in vivo , by the activation of the insulin signaling pathway, accomplished by the suppression of oxidative stress.
Keyphrases
- type diabetes
- signaling pathway
- oxidative stress
- transcranial magnetic stimulation
- protein kinase
- glycemic control
- insulin resistance
- pi k akt
- high frequency
- induced apoptosis
- nuclear factor
- adipose tissue
- dna damage
- ischemia reperfusion injury
- epithelial mesenchymal transition
- high fat diet induced
- cardiovascular disease
- weight loss
- metabolic syndrome
- randomized controlled trial
- blood glucose
- physical activity
- endothelial cells
- protein protein
- low dose
- toll like receptor
- blood pressure
- binding protein
- intellectual disability
- autism spectrum disorder
- inflammatory response
- polycystic ovary syndrome
- tyrosine kinase
- heat stress
- study protocol
- small molecule
- heat shock