Inhibitive Effects of Mulberry Leaf-Related Extracts on Cell Adhesion and Inflammatory Response in Human Aortic Endothelial Cells

• Published in: Evidence-based complementary and alternative medicine 2013-01, Vol.2013 (2013), p.1-14
• Main Authors: Chiu, C.-C., Chao, P.-Y., Yang, C.-M., Huang, M.-Y., Yang, Y.-Y., Lin, K.-H.
• Format: Article
• Language: English
• Subjects: Adhesion; Antioxidants; Aorta; Apoptosis; Atherosclerosis; Cell adhesion; Cell adhesion & migration; Comet assay; Deoxyribonucleic acid; Diabetes; DNA; DNA damage; Endothelial cells; Flavonoids; Flavonols; Human behavior; Hydrogen peroxide; Inflammation; Inflammatory response; Kaempferol; Leaves; Lymphocytes; Metabolites; Monocytes; NF-κB protein; Nutrition; Peroxisome proliferator-activated receptors; Polyphenols; Quercetin; Tea; Toxicity; Transcription factors; Tumor necrosis factor-TNF; Tumor necrosis factor-α; Vitamin E
• ISSN: 1741-427X; 1741-4288
• DOI: 10.1155/2013/267217

Effects of mulberry leaf-related extracts (MLREs) on hydrogen peroxide-induced DNA damage in human lymphocytes and on inflammatory signaling pathways in human aortic endothelial cells (HAECs) were studied. The tested MLREs were rich in flavonols, especially bombyx faces tea (BT) in quercetin and kaempferol. Polyphenols, flavonoids, and anthocyanidin also abounded in BT. The best trolox equivalent antioxidant capacity (TEAC) was generated from the acidic methanolic extracts of BT. Acidic methanolic and water extracts of mulberry leaf tea (MT), mulberry leaf (M), and BT significantly inhibited DNA oxidative damage to lymphocytes based on the comet assay as compared to the H2O2-treated group. TNF-α-induced monocyte-endothelial cell adhesion was significantly suppressed by MLREs. Additionally, nuclear factor kappa B (NF-κB) expression was significantly reduced by BT and MT. Significant reductions were also observed in both NF-κB and activator protein (AP)-1 DNA binding by MLREs. Significant increases in peroxisome proliferator-activated receptor (PPAR) α and γ DNA binding by MLREs were also detected in M and MT extracts, but no evidence for PPAR α DNA binding in 50 μg/mL MT extract was found. Apparently, MLREs can provide distinct cytoprotective mechanisms that may contribute to its putative beneficial effects on suppressing endothelial responses to cytokines during inflammation.