Journal
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY
Volume 19, Issue 10, Pages 1697-1704Publisher
AMER SCIENTIFIC PUBLISHERS
DOI: 10.1166/jbn.2023.3681
Keywords
Abdominal Aortic Aneurysm; Resveratrol; Sirtuin 1; Endothelial Cells; eNOS Activity
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This study investigated the mechanism underlying the inhibitory effect of resveratrol nanoparticles on AAA endothelial dysfunction. It was found that resveratrol nanoparticles can reduce endothelial cell proliferation and migration and induce apoptosis.
Abdominal aortic aneurysm (AAA) is a pathological condition of chronic dilation of the aorta. This study investigated the mechanism underlying the inhibitory effect of resveratrol nanoparticles on AAA endothelial dysfunction. Mice in the control group received normal saline (n = 18) while those in the model group (n = 18) were implanted with Alzet microp-umps to induce AAA. After modeling, the endothelial cells of abdominal aortic tissue were collected and treated with resveratrol nanoparticles and resveratrol nanoparticles plus sirtuin 1 (SIRT1) (resveratrol nanoparticles + SIRT1 group). CCK-8 method detected proliferation ability of abdominal aortic endothelial cells, flow cytometry assessed cell apopto-sis, and transwell method measured the migration ability along with analysis of SIRT1 level, eNOS and NO content. IP 2038 10920 On: Sun 29 Oct 2023 0550:28 The proliferation ability of endothelial cells was significantly derased in resveratrol nanoparticles group (0.41 +/- 0.04, Copyright: American Scientific Publishers 0.60 +/- 0.05, 0.69 +/- 0.04) and resveratrol + SIRT1 group (0.37 +/- 0.05, 0.49 +/- 0.04, 0.57 +/- 0.04), with lower proliferation in Delivered by Ingenta resveratrol + SIRT1 group (P < 0.05). Treatment resulted in enhancement of endothelial cell apoptosis and decreased migration ability (P < 0.05), as the effect of combined treatment was more significant. Moreover, resveratrol nanoparti-cles (0.44 +/- 0.02, 0.34 +/- 0.05) or resveratrol nanoparticles plus SIRT1 (0.50 +/- 0.01, 0.44 +/- 0.03) increased SIRT1 level (P < 0.05), eNOS activity and NO secretion (P < 0.05) in the resveratrol + SIRT1 group. Resveratrol nanoparticles can reduce endothelial cell proliferation and migration and induce apoptosis when increasing SIRT1 expression.
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