Dietary Methionine Restriction Improves Gastrocnemius Muscle Glucose Metabolism through Improved Insulin Secretion and H19/IRS-1/Akt Pathway in Middle-Aged Mice.
Chuanxing FengYuge JiangGuoqing WuYonghui ShiYueting GeBowen LiXiangrong ChengXue TangJianjin ZhuGuowei LePublished in: Journal of agricultural and food chemistry (2023)
Methionine restriction (MR) improves glucose metabolism. In skeletal muscle, H19 is a key regulator of insulin sensitivity and glucose metabolism. Therefore, this study aims to reveal the underlying mechanism of H19 upon MR on glucose metabolism in skeletal muscle. Middle-aged mice were fed MR diet for 25 weeks. Mouse islets β cell line β-TC6 cells and mouse myoblast cell line C2C12 cells were used to establish the apoptosis or insulin resistance model. Our findings showed that MR increased B-cell lymphoma-2 (Bcl-2) expression, deceased Bcl-2 associated X protein (Bax), cleaved cysteinyl aspartate-specific proteinase-3 (Caspase-3) expression in pancreas, and promoted insulin secretion of β-TC6 cells. Meanwhile, MR increased H19 expression, insulin Receptor Substrate-1/insulin Receptor Substrate-2 (IRS-1/IRS-2) value, protein Kinase B (Akt) phosphorylation, glycogen synthase kinase-3β (GSK3β) phosphorylation, and hexokinase 2 (HK2) expression in gastrocnemius muscle and promoted glucose uptake in C2C12 cells. But these results were reversed after H19 knockdown in C2C12 cells. In conclusion, MR alleviates pancreatic apoptosis and promotes insulin secretion. And MR enhances gastrocnemius muscle insulin-dependent glucose uptake and utilization via the H19/IRS-1/Akt pathway, thereby ameliorating blood glucose disorders and insulin resistance in high-fat-diet (HFD) middle-aged mice.
Keyphrases
- induced apoptosis
- cell cycle arrest
- skeletal muscle
- insulin resistance
- high fat diet
- endoplasmic reticulum stress
- signaling pathway
- middle aged
- blood glucose
- poor prognosis
- cell death
- type diabetes
- protein kinase
- contrast enhanced
- pi k akt
- oxidative stress
- cell proliferation
- binding protein
- long non coding rna
- high fat diet induced
- glycemic control
- adipose tissue
- transcription factor
- gene expression
- metabolic syndrome
- amino acid
- endothelial cells
- physical activity