Table 1.
Host | Effects | Extract/Doses | Reference |
---|---|---|---|
Rats | Reduced weight gain Decreased blood glucose levels |
Leaf extract (infusion ad libitum) | [49] |
Decreased blood glucose levels Inhibited hepatic glycogen loss Preserved histopathological alterations in the pancreas without glomerular alterations |
Leaf decoction (20g/L) | [50] | |
Mice | Demonstrated antiplatelet, antithrombotic without cytotoxic effects and gastric lesions | Leaf extract (30 and 100 mg/kg/day) and ASA (100 mg/kg/day) | [45] |
Attenuated proinflammatory markers, such as IL-6, IL-1, TNF-α, and IFN-γ Increased IL-10 Only C. xanthocarpa was able to decrease anti-oxLDL antibodies without ulcerogenic activity |
Leaf extract (100 mg/kg/day) and ASA (100 mg/kg/day) | [58] | |
Rats | Decreased blood pressure in a dose-dependent manner (50 mg/kg) Reduced heart rate (50 to 200 mg/kg) |
Leaf extract (25, 50, 75, 100, 125, 150, 175, and 200 mg/kg) | [47] |
Humans | Decreased LDL-c and total cholesterol levels without differences in triglyceride, VLDL-c, or HDL-c levels Reduced inflammation and oxidative stress Displayed protective effects on the endothelium. |
Encapsulated leaf extract (500 mg, 750 mg or 1000 mg) | [42] |
Demonstrated antiplatelet effects | Leaf extract (1000 mg), ASA (100 mg), ASA (50 mg) + leaf extract (500 mg) | [46] |
Principal studies of C. xanthocarpa in metabolic disorders accomplished in animal models (in vivo) and human clinical trials.