Chen Mingliang,Yi Long,Jin Xin,Xie Qi,Zhou Xi,Chen Chunye,Zhang Ting,Wang Li,Mi Mantian.Effect of resveratrol on TNF-α-induced vascular endothelial inflammation in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(13):1255-1258.
Chen Mingliang,Yi Long,Jin Xin,Xie Qi,Zhou Xi,Chen Chunye,Zhang Ting,Wang Li,Mi Mantian.Effect of resveratrol on TNF-α-induced vascular endothelial inflammation in vitro[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(13):1255-1258.DOI:
Effect of resveratrol on TNF-α-induced vascular endothelial inflammation in vitro
Objective To determine the inhibitory effects of resveratrol on TNF-α induced inflammatory damage in vascular endothelial cell line EA. hy926. Methods After the endothelial EA. hy926 cells were treated with TNF-α of different concentrations (0.01
0.1
1
2.5
5
10
20
50
100
200
and 400 ng/ml) for 24 h
cell viability and sICAM-1 release in the supernatant were measured by MTT and ELISA assay
respectively. Cells were pretreated with resveratrol of different concentrations (0.1
1
and 10 μmol/L) for 24 h
and then incubated with TNF-α (10 ng/ml) for another 24 h. sICAM-1 level in the the supernatant was determined by sICAM-1 ELISA kit. The mRNA expression of intercellular adhesion molecule-1 (ICAM-1) and tumor necrosis factor receptor-1 (TNFR1) were measured by qRT-PCR assay. Results After treated with TNF-α at high concentration (≥100 ng/ml)
cell viability was decreased significantly. Cell viability incubated with 200 ng/ml TNF-α was decreased by about 59.7% compared with control. When treated with a low concentration of TNF-α (10 ng/ml)
the mRNA levels of ICAM-1 and TNFR1 were increased markedly (P0.05). However
resveratrol pretreatment significantly (P0.01) inhibited the increase of ICAM-1 and TNFR1 mRNA expression induced by TNF-α in a dose-dependent manner. Conclusion Resveratrol might inhibit the TNF-α-induced inflammatory cytokine release and alleviate endothelial inflammation by inhibiting TNFR1-mediated signaling pathway.
Resveratrol protects human umbilical vein endothelial cells against oxidative injury by activating transcription factor EB in vitro
Role of SIRT1/UCP2 signaling pathway in resveratrol-induced inhibition of oxidative injury in vascular endothelial cells
Construction and verification of a nomogram prediction model for vascular plaque stability in patients with progressive cerebral infarction based on serum MCP-1, MCPIP1 combined with inflammatory factors
Dihydromyricetin ameliorates vascular endothelial damage by inhibiting NLRP3 inflammasome activity through Sirtuin 3
Resveratrol promotes hepatic lipid decomposition by regulating ATGL/CGI58 and Rab7/LC3β through perilipin 2
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