Biochanin A Mitigates Atherosclerosis by Inhibiting Lipid Accumulation and Inflammatory Response

Oxid Med Cell Longev. 2020 Nov 11:2020:8965047. doi: 10.1155/2020/8965047. eCollection 2020.

Abstract

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.

MeSH terms

  • ATP Binding Cassette Transporter 1 / metabolism
  • ATP Binding Cassette Transporter, Subfamily G, Member 1 / metabolism
  • Animals
  • Atherosclerosis / blood*
  • Atherosclerosis / drug therapy*
  • Atherosclerosis / etiology
  • Brassica / chemistry*
  • Cholesterol / metabolism
  • Cytokines / blood
  • Diet, Western / adverse effects
  • Disease Models, Animal
  • Foam Cells / drug effects
  • Foam Cells / metabolism
  • Genistein / administration & dosage*
  • Heme Oxygenase-1 / metabolism
  • Humans
  • Inflammation / drug therapy
  • Inflammation / metabolism
  • Lipid Metabolism / drug effects*
  • Lipids / blood
  • Liver X Receptors / metabolism
  • Male
  • Mice
  • Mice, Knockout, ApoE
  • PPAR gamma / metabolism
  • Phytotherapy / methods*
  • Plant Extracts / administration & dosage*
  • Protective Agents / administration & dosage*
  • Signal Transduction / drug effects
  • THP-1 Cells
  • Trifolium / chemistry*

Substances

  • ABCA1 protein, human
  • ABCG1 protein, human
  • ATP Binding Cassette Transporter 1
  • ATP Binding Cassette Transporter, Subfamily G, Member 1
  • Cytokines
  • Lipids
  • Liver X Receptors
  • NR1H3 protein, human
  • PPAR gamma
  • PPARG protein, human
  • Plant Extracts
  • Protective Agents
  • Cholesterol
  • Genistein
  • HMOX1 protein, human
  • Heme Oxygenase-1
  • biochanin A