Extract of Unifloral Camellia sinensis L. Pollen Collected by Apis mellifera L. Honeybees Exerted Inhibitory Effects on Glucose Uptake and Transport by Interacting with Glucose Transporters in Human Intestinal Cells.
Qiangqiang LiCaijun RenSha YanKai WangYuliya HrynetsLei XiangXiaofeng XueMirko BettiLiming WuPublished in: Journal of agricultural and food chemistry (2021)
Bee pollen possesses potential hypoglycemic effects but its inhibitory mechanisms on glucose absorption and transportation in intestinal cells still need to be clarified. Here, we determined the inhibitory effects of bee pollen extract originating from Camellia sinensis L. (BP-Cs) as well as its representative phenolic compounds on glucose uptake and transport through a human intestinal Caco-2 cell monolayer model. It showed that three representative phenolic compounds, including gallic acid (GA), 3-O-[6'-O-(trans-p-coumaroyl)-β-d-glucopyranosyl]kaempferol (K1), and 3-O-[2',6'-di-O-(trans-p-coumaroyl)-β-d-glucopyranosyl]kaempferol (K2), with contents of 27.7 ± 0.86, 9.88 ± 0.54, and 7.83 ± 0.46 μg/mg in BP-Cs extract, respectively, exerted mutual antagonistic actions interacting with glucose transporters to inhibit glucose uptake and transport based on their combination index (CI) and molecular docking analysis. K1, K2, and GA might compete with d-glucose to form hydrogen bonds with the same active residues including GLU-412, GLY-416, GLN-314, and TRP-420 in GLUT2. These findings provide us a deep understanding of the mechanisms underlying the anti-hyperglycemia by bee pollen, which provide a new sight on dietary intervention strategies against diabetes.
Keyphrases
- blood glucose
- molecular docking
- endothelial cells
- induced apoptosis
- oxidative stress
- pet ct
- type diabetes
- randomized controlled trial
- stem cells
- cardiovascular disease
- risk assessment
- anti inflammatory
- metabolic syndrome
- single cell
- cross sectional
- glycemic control
- cell death
- adipose tissue
- mesenchymal stem cells
- biofilm formation
- cell proliferation
- cystic fibrosis
- endoplasmic reticulum stress
- staphylococcus aureus
- insulin resistance
- induced pluripotent stem cells
- pluripotent stem cells
- pi k akt
- candida albicans