Attenuating Effects of Pyrogallol-Phloroglucinol-6,6-Bieckol on Vascular Smooth Muscle Cell Phenotype Changes to Osteoblastic Cells and Vascular Calcification Induced by High Fat Diet.
Myeongjoo SonSeyeon OhJi Tae JangChul-Hyun ParkKuk Hui SonKyunghee ByunPublished in: Nutrients (2020)
Advanced glycation end products/receptor for AGEs (AGEs/RAGEs) or Toll like receptor 4 (TLR4) induce vascular smooth muscle cell (VSMC) phenotype changes in osteoblast-like cells and vascular calcification. We analyzed the effect of Ecklonia cava extract (ECE) or pyrogallol-phloroglucinol-6,6-bieckol (PPB) on VSMC phenotype changes and vascular calcification prompted by a high-fat diet (HFD). HFD unregulated RAGE, TLR4, transforming growth factor beta (TGFβ), bone morphogenetic protein 2 (BMP2), protein kinase C (PKC), and nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) signals in the aorta of mice. ECE and PPB restored the increase of those signal pathways. AGE- or palmitate-treated VSMC indicated similar changes with the animal. HFD increased osteoblast-like VSMC, which was evaluated by measuring core-binding factor alpha-1 (CBFα-1) and osteocalcin expression and alkaline phosphatase (ALP) activity in the aorta. ECE and PPB reduced vascular calcification, which was analyzed by the calcium deposition ratio, and Alizarin red S stain was increased by HFD. PPB and ECE reduced systolic, diastolic, and mean blood pressure, which increased by HFD. PPB and ECE reduced the phenotype changes of VSMC to osteoblast-like cells and vascular calcification and therefore lowered the blood pressure.
Keyphrases
- high fat diet
- nuclear factor
- toll like receptor
- blood pressure
- smooth muscle
- insulin resistance
- adipose tissue
- transforming growth factor
- inflammatory response
- chronic kidney disease
- left ventricular
- metabolic syndrome
- heart failure
- type diabetes
- heart rate
- oxidative stress
- binding protein
- single cell
- cell therapy
- stem cells
- epithelial mesenchymal transition
- poor prognosis
- mesenchymal stem cells
- transcription factor
- cell proliferation
- induced apoptosis
- pulmonary artery
- bone regeneration
- endoplasmic reticulum stress
- long non coding rna
- bone marrow
- atrial fibrillation
- ejection fraction
- angiotensin ii