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Structure · dataset · 2022

Protective roles of apremilast via Sirtuin 1 in atherosclerosis

Listed in Loughborough Research Repository and GRANTS Data and UP Research Data Repository — shown once because both records carry DOI 10.6084/m9.figshare.20078617.v2

<p>Atherosclerosis is an inflammatory disease with a high level of cholesterol in the blood.

Description

Apremilast is a new anti-inflammatory drug that possesses a potential anti-atherosclerosis effect. RT-qPCR and western blot were undertaken to assay the levels of Sirtuin 1 (SIRT1), oxidized low density lipoprotein receptor 1 (LOX-1), and CD36 molecule (CD36).

Reactive oxygen species (ROS) levels were evaluated by 2’, 7’-dichlorodihydrofluorescein diacetate (DCFH-DA) staining, and Oil Red O staining was performed to show lipid accumulation. The result showed that apremilast treatment reduced the expression levels of pro-inflammatory factors and p-p65, as well as lipid accumulation. Meanwhile, triglyceride (TG), total cholesterol (TC) and free cholesterol (FC) levels declined in oxidized low density lipoprotein (ox-LDL)-treated macrophages.

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Mechanistically, apremilast targets SIRT1 and increases SIRT1 expression. The efficacy of apremilast on inflammatory response and lipid formation required the involvement of SIRT1. Additionally, apremilast treatment reduced scavenger receptors, LOX-1, and CD36 levels.

These findings suggest the protective effects of apremilast via SIRT1 in atherogenesis and highlight the need for translational research from bench to bedside.</p>

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Inferred from text
Disease 75%
Provenance · 3 source records, 42 field assertions
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Loughborough Research Repositoryoai:figshare.com:article/2007861710 d agoJSON v1
GRANTS Dataoai:figshare.com:article/2007861710 d agoJSON v1
UP Research Data Repositoryoai:figshare.com:article/200786179 d agoJSON v1
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