Table 3.
Genistein effects on lipids profile.
| Study Design | Doses | Route of administration | Effects | Ref |
|---|---|---|---|---|
| HepG2 cells cultured | 0, 0.01, 1.00, 10.00, and 50.00 µM | Expose | ↑Total-cholesterol levels ↓HDL-C ↓Apo-A1 ↑Sterol regulatory element binding proteins-2)SREBP-2) at protein and mRNA levels ↑Low-density lipoprotein receptor (LDLR) mRNA levels ↑3-hydroxy-3-methyl glutaryl coenzyme A reductase (HMGCR) ↑Intracellular cholesterol synthesis ↓MRNA levels of (PPARγ) ↓X receptor of liver (LXRα) ↓LXRα and ATP-binding cassette transporter A1 (ABCA1) protein levels ↑Intracellular cholesterol levels ↑SREBP-2/LDLR/HMGCR pathway ↓PPARγ/LXRα/ABCA1 pathway ↓Cholesterol plasma levels ↑Cholesterol absorption ↓Cholesterol efflux |
[43] |
|
| ||||
| Human umbilical vein endothelial cells (HUVECs) | 1000 nM | Pretreated with genistein | ↓Ox-LDL induced senescence ↓SA-β-gal activity and P16 and P21 protein ↑Autophagic flux ↑LC3-II, ↓p-P70S6K, p-mTOR, and P62 level |
[44] |
|
| ||||
| Rats | 50 mg/kg | Gavaged | ↓Triglyceride and HDL level more than LCG or LC ↓TNF-α, and IL-6 |
[45] |
|
| ||||
| Rats | 20 mg/kg | Gavage | ↓Levels of malondialdehyde (MDA) ↓TNF-α ↑Superoxide dismutase activity ↓Luteinization ↓Inflammatory cytokines |
[46] |
|
| ||||
| Rats | 10 mg/kg/day | Expose | ↓LDL cholesterol ↓Total cholesterol levels |
[47] |
|
| ||||
| Rats | 600 mg/kg diet | In the diet | ↑Plasma insulin level ↓HbA(1C) level ↑Glucokinase level ↓Hyperglycemia and Glucose-6-phosphatase |
[48] |
|
| ||||
| Rats | 200 ppm | A 4-week feeding study | ↓Serum cholesterol ↑Total and trabecular bone mineral density |
[49] |
|
| ||||
| Rats | 10 mg/kg | Subcutaneous administration | ↓Total cholesterol levels ↓Lipoprotein cholesterol levels ↑TT levels ↓Serum cholesterol levels ↑Serum triglycerides |
[50] |
|
| ||||
| Hamsters | 2 g/kg | Diet | ↓Hyperlipidemia ↓Triglyceride and LDL cholesterol ↓Malondialdehyde ↓Liver and plasma cholesterol ↑Hepatic LDL receptor ↑ α and β mRNA receptors of estrogen |
[51] |
|
| ||||
| Volunteers human | 250 μmol/L | Was dissolved in dimethyl sulfoxide injection | ↓Agonist-induced platelet aggregation ↓Collagen- and ADP-dependent platelet activation ↓Coronary atherosclerosis ↓Platelet activity |
[52] |
|
| ||||
| Human | 0.5–2.5 microM | Subjects consuming | ↓Lipid peroxidation of HDL ↑Conjugated dienes ↓Alterations of apoprotein structure |
[53] |
|
| ||||
| Women | 90 mg/day | Supplement for 12 week | ↓ Triglyceride levels ↓Total cholesterol ↓Ldl |
[54] |
|
| ||||
| Postmenopausal women | 54 mg | PO for 24 month | ↓Fasting glucose ↓HOMA-IR and insulin ↓Homocysteine and Fibrinogen |
[55] |
|
| ||||
| Postmenopausal women | 60 mg/day | Genistein or placebo capsule | ↓Total cholesterol, LDL-C, and TG levels ↑HDL-C levels ↑Expression of LDLR, LXRα, and ABCG1 ↓Cholesterol |
[56] |