Whole Grain Proso Millet ( Panicum miliaceum L. ) Attenuates Hyperglycemia in Type 2 Diabetic Mice: Involvement of miRNA Profile.
Xu DengJiayi LiangLehui WangLi NiuJin XiaoQianqian GuoXuebo LiuChunxia XiaoPublished in: Journal of agricultural and food chemistry (2023)
This work aimed to investigate the hypoglycemic effects and underlying mechanism of whole grain proso millet ( Panicum miliaceum L. ; WPM) on type 2 diabetes mellitus (T2DM). The results showed that WPM supplementation significantly reduced fasting blood glucose (FBG) and serum lipid levels in T2DM mice induced by a high-fat diet (HFD) combined with streptozotocin (STZ), with improved glucose tolerance, liver and kidney injury, and insulin resistance. In addition, WPM significantly inhibited the expression of gluconeogenesis-related genes G6pase , Pepck , Foxo1 , and Pgc -1α . Further study by miRNA high-throughput sequencing revealed that WPM supplementation mainly altered the liver miRNA expression profile of T2DM mice by increasing the expression of miR-144-3p_R-1 and miR-423-5p, reducing the expression of miR-22-5p_R-1 and miR-30a-3p. GO and KEGG analyses showed that the target genes of these miRNAs were mainly enriched in the PI3K/AKT signaling pathway. WPM supplementation significantly increased the level of PI3K, p-AKT, and GSK3β in the liver of T2DM mice. Taken together, WPM exerts antidiabetic effects by improving the miRNA profile and activating the PI3K/AKT signaling pathway to inhibit gluconeogenesis. This study implies that PM can act as a dietary supplement to attenuate T2DM.
Keyphrases
- signaling pathway
- high fat diet
- blood glucose
- glycemic control
- poor prognosis
- pi k akt
- insulin resistance
- high fat diet induced
- adipose tissue
- type diabetes
- epithelial mesenchymal transition
- induced apoptosis
- diabetic rats
- cell proliferation
- transcription factor
- particulate matter
- weight loss
- high throughput sequencing
- air pollution
- binding protein
- heavy metals
- cardiovascular disease
- oxidative stress
- single cell
- long non coding rna
- endoplasmic reticulum stress
- fatty acid