Abstract

Endothelial-to-mesenchymal transition (EndMT), which is involved in the development of various cardiovascular diseases, is induced by dyslipidemia or obesity. In dyslipidemia, the increased levels of oxidized low-density lipoproteins (oxLDL) upregulated the lectin-type oxidized LDL receptor 1 (Lox-1), which then upregulated the down signaling pathways of PKC-α/MMPs/TGF-β/SMAD2 or 3 and increased the EndMT. In this study, we investigated the effect of pyrogallol-phloroglucinol-6,6-bieckol (PPB), which is a compound of Ecklonia cava (E. cava), on decreased blood pressure (BP) by attenuating the EndMT in a high-fat diet- (HFD-) fed animal model. We also investigated PPB's attenuation effect on EndMT in oxLDL-treated mouse endothelial cells as an in vitro model. The results indicated that, in the aorta or endothelial cells of mice, the HFD or oxLDL treatment significantly increased the expression of Lox-1/PKC-α/MMP9/TGF-β/SMAD2/SMAD3. The PPB treatment significantly decreased its expression. In contrast, the HFD or oxLDL treatment significantly decreased the expression of the EC markers (PECAM-1 and vWF) while the PPB treatment significantly increased them. Moreover, the HFD or oxLDL treatment significantly increased the expression of the mesenchymal cell markers (α-SMA and vimentin) while PPB treatment significantly decreased them. PPB decreased the intima-media thickness and extracellular matrix amount of the aorta and attenuated the BP, which was increased by the HFD. In conclusion, PPB attenuated the upregulation of Lox-1/PKC-α/MMP9/TGF-β/SMAD2 and 3 and restored the EndMT in HFD-fed animals. Moreover, PPB showed a restoring effect on HFD-induced hypertension.

Highlights

  • Neointimal hyperplasia is the main pathophysiology of many cardiovascular diseases, such as atherosclerosis and hypertension [1]

  • Endothelial cell (EC) could be a source of smooth, muscle-like cells migrating through the endothelial-to-mesenchymal transition (EndMT), which is involved in the neointimal hyperplasia processes [1, 3]

  • We evaluated the effect of PPB on EndMT induced by oxidized low-density lipoproteins (oxLDL) in an in vitro model and EndMT induced by a high-fat diet (HFD) in an animal model

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Summary

Introduction

Neointimal hyperplasia is the main pathophysiology of many cardiovascular diseases, such as atherosclerosis and hypertension [1]. Oxidative Medicine and Cellular Longevity adhesion molecule-1 (PECAM-1 or CD31) are decreased, the mesenchymal markers such as alpha-smooth muscle actin (α-SMA), N-cadherin, vimentin, fibronectin, and calponin are increased [6, 7]. Many triggering factors, such as shear stress, hyperglycemia, dyslipidemia, and hyperhomocystinuria, induce EndMT [8, 9]. We evaluated the effect of PPB on the regulation of Lox-1/PKC/MMP9, which leads to the upregulation of TGF-β/SMAD2 and 3 and decreased HFDinduced BP

Materials and Methods
2.10. Angiogenesis Assay
Results
Discussion
Conclusions
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