Table 1.
Polyphenolic Compounds | Chemical Structure | Dose | Model | Effect on GLP1 | Possible Mechanisms |
---|---|---|---|---|---|
Curcumin [125,127] | 10 μM 1.5 mg/kg b.w. |
Glutag L-cells, Rat |
Increase GLP-1 secretion; increase plasma GLP-1 level | GPR40/120-dependent pathway | |
Delphinidin 3-rutinoside [128] | 10 μM | Glutag L-cells |
Increase GLP-1 secretion | GPR40/120-dependent pathway | |
EGCG [145,146,147] | 300 μM 500 mg |
Mouse ileum segment, diabetic patients | Increase GLP-1 secretion; increase plasma GLP-1 level | Tas2Rs-dependent pathway | |
Genistein [165] | 20 mg/kg b.w. | Alloxan-induced insulin deficient diabetic rats [165] | Increase tissue content of GLP-1 | cAMP signaling by activating AC | |
Grifolic acid [132] | 30 μM | STC-1 cells | Increase GLP-1 secretion | GPR120/Ca2+ signaling | |
Grifolic acid methyl ether [132] | 30 μM | STC-1 cells | Increase GLP-1 secretion | GPR120/Ca2+ signaling | |
Hispidulin [166] | 1 μM 20 mg/kg b.w. |
Glutag L-cell, STZ-induced diabetic mice |
Increase GLP-1 secretion; increase plasma GLP-1 level | Inhibiting PDE activity | |
Silymarin [169] | 100 mg/kg b.w. | Obese rats | Increased serum GLP-1 level | Inhibiting PDE activity | |
Caffeoylquinic acid [173] | IC50: 0.49 mM | Human plasma platelets | Not applicable | Inhibiting PDE activity | |
Caffeic acid [173] | IC50: 0.48 mM | Human plasma platelets | Not applicable | Inhibiting PDE activity |