| Literature DB >> 29951871 |
Feng Zheng1, Xiaomeng Dong2, Xiangzhu Meng2.
Abstract
In the present study, we used the human umbilical vein endothelial cells (HUVECs) to investigate the anti-inflammatory effects and mechanism of taraxasterol on vascular inflammation. HUVECs were pre-treated with taraxasterol 1 h before lipopolysaccharide (LPS) treatment. The concentrations of TNF-α, IL-8, PGE2, and NO were measured. The expression of VCAM-1, ICAM-1, iNOS, COX-2, NF-κB, and LXRα was detected by western blot analysis. The results showed that taraxasterol not only reduced the production of TNF-α, IL-8, PGE2, and NO induced by LPS, but also reduced the expression of iNOS and COX-2. Taraxasterol also suppressed LPS-induced NF-κB activation and VCAM-1 and ICAM-1 expression. Furthermore, taraxasterol concentration-dependently increased the expression of LXRα. The inhibition of taraxasterol on TNF-α, IL-8, PGE2, and NO production can be reversed by geranylgeranyl diphosphate (GGPP, the LXRα inhibitor). Here, we found that taraxasterol inhibited vascular inflammation through activating LXRα.Entities:
Keywords: LXRα; NF-κB; VCAM-1; human umbilical vein endothelial cells; taraxasterol
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Year: 2018 PMID: 29951871 DOI: 10.1007/s10753-018-0818-3
Source DB: PubMed Journal: Inflammation ISSN: 0360-3997 Impact factor: 4.092