Low (≦1 μM) to Moderate
|
|
|
0.1‒10 μM
|
Diminish PMA‒induced neutrophil activation and reduce neutrophil adhesion ability
|
[44]
|
Moderate (1–100 μM)
|
|
|
5‒10 μM
|
Inhibited TNFα‒induced VACM‒1 expression in aortic endothelial cells
|
[37]
|
10 μM
|
Inhibit proliferation of cardiac fibroblasts
|
[23]
|
16.8 μM
|
Inhibit LPS‒induced macrophage activation
|
[35]
|
5‒20 μM
|
Induce intrinsic apoptosis in vascular smooth muscle cells
|
[25]
|
5‒20 μM
|
Inhibit TNFα‒induced vascular smooth muscle cell proliferation
|
[27]
|
>20 μM
|
Downregulate IL‒6‒induced ICAM‒1 expression in endothelial cells and suppress monocyte adhesion to endothelial cells
|
[41]
|
2.5‒20 μM
|
Inhibit copper‒induced ox‒LDL triggered endothelial cell apoptosis
|
[33,34]
|
24.2 μM
|
Inhibit neutrophil aggregation
|
[38]
|
3‒30 μM
|
Inhibit collagen‒induced platelet serotonin release
|
[43]
|
5‒50 μM
|
Suppress fMLP‒activated neutrophil migration
|
[20]
|
30‒90 μM
|
induce cytosolic‒free Ca2+ elevation in neutrophil
|
[36]
|
Moderate to High (≧100 μM)
|
|
|
200 μM
|
Reduce serum‒induced vascular smooth muscle cell proliferation
|
[26]
|
40‒400 μM
|
block norepinephrine‒ or high K+−induced contraction of aorta
|
[30]
|
60‒150 μM |
Inhibit biosynthesis of platelet‒activating factor from PMNs |
[44] |