Biochanin A Mitigates Atherosclerosis by Inhibiting Lipid Accumulation and Inflammatory Response.
Xiao-Hua YuJiao-Jiao ChenWen-Yi DengXiao-Dan XuQi-Xian LiuMeng-Wen ShiKun RenPublished in: Oxidative medicine and cellular longevity (2020)
Biochanin A (BCA), a dietary isoflavone extracted from red clover and cabbage, has been shown to antagonize hypertension and myocardial ischemia/reperfusion injury. However, very little is known about its role in atherogenesis. The aim of this study was to observe the effects of BCA on atherosclerosis and explore the underlying mechanisms. Our results showed that administration of BCA promoted reverse cholesterol transport (RCT), improved plasma lipid profile, and decreased serum proinflammatory cytokine levels and atherosclerotic lesion area in apoE-/- mice fed a Western diet. In THP-1 macrophage-derived foam cells, treatment with BCA upregulated ATP-binding cassette (ABC) transporter A1 (ABCA1) and ABCG1 expression and facilitated subsequent cholesterol efflux and diminished intracellular cholesterol contents by activating the peroxisome proliferator-activated receptor γ (PPARγ)/liver X receptor α (LXRα) and PPARγ/heme oxygenase 1 (HO-1) pathways. BCA also activated these two signaling pathways to inhibit the secretion of proinflammatory cytokines. Taken together, these findings suggest that BCA is protective against atherosclerosis by inhibiting lipid accumulation and inflammatory response through the PPARγ/LXRα and PPARγ/HO-1 pathways. BCA may be an attractive drug for the prevention and treatment of atherosclerotic cardiovascular disease.
Keyphrases
- cardiovascular disease
- inflammatory response
- signaling pathway
- insulin resistance
- ischemia reperfusion injury
- induced apoptosis
- pi k akt
- blood pressure
- low density lipoprotein
- lipopolysaccharide induced
- poor prognosis
- fatty acid
- type diabetes
- lps induced
- binding protein
- oxidative stress
- adipose tissue
- high fat diet induced
- toll like receptor
- epithelial mesenchymal transition
- left ventricular
- skeletal muscle
- coronary artery disease
- high fat diet
- long non coding rna
- cognitive decline
- dna binding
- transcription factor
- south africa
- cell proliferation
- combination therapy
- cardiovascular risk factors
- cell death
- drug induced
- atrial fibrillation
- adverse drug