Anti-inflammation effect of genistein and daidzein on oxidised low-density lipoprotein-simulated human coronary artery endothelial cells

• Main Author: Lina Izzati Amer (Author)
• Format: Thesis Book
• Language: English
• Published: Sungai Buloh, Selangor Universiti Teknologi MARA. Faculty of Medicine 2019
• Subjects: Phytoestrogens > therapeutic use; Inflammation > physiopathology; Chronic Disease > prevention & control
• Online Access: Click Here to View Status and Holdings.
• Item Description: UiTM Digitized
• Physical Description: xv, 96 pages illustrations (some color), charts 30 cm
• Bibliography: Includes bibliographical references (page 63-85)

Oxidised low-density lipoprotein (OxLDL) exerts adverse reaction to the endothelial cells in chronic oxidative disorder like atherosclerosis. Adhesion molecules such as VCAM-1 and ICAM-1, are regarded as key inflammatory markers promoting the endothelial cell injury, whereas nitric oxide regulates the disease process under OxLDL exposure. Isoflavones, genistein and daidzein, possess anti-inflammatory effects to improve the endothelial deterioration. However, the effects of genistein and daidzein on OxLDL stimulated endothelial injury and its inflammatory changes remain unexplored. In this study, the anti-inflammation role of genistein and daidzein on human coronary artery endothelial cells (HCAECs) under OxLDL exposure was investigated. The cells stimulated with 100 ug/mL of OxLDL showed reduced in cell viability rate. Different concentrations of genistein and daidzein were used as treatment for OxLDL stimulated HCAECs. VCAM-1 and ICAM-1 along with endothelial nitric oxide synthase (NOS), were analysed quantitatively by expression of ELISA and supported by the immunofluorescence staining. Following treatment with low concentration of genistein at 6.25 ug/ml and high concentrations of daidzein at 12.5 and 25 ug/ml showed lower expression of VCAM-1 and ICAM-1 which regulated the progression of OxLDL-stimulated endothelial injury in HCAECs. Increased level of eNOS was observed in genistein and daidzein treated groups when compared to the untreated OxLDL group. Our study showed that genistein and daidzein, improved the endothelial cell viability, eNOS production and reduced inflammatory reactions under OxLDL exposure. Thus, genistein and daidzein were believed to have potential therapeutic effect in rescuing endothelial cells against OXLDL