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鞣花酸抑制白细胞介素-1β诱导的人脐静脉内皮细胞中细胞黏附分子的表达。

Ellagic acid inhibits IL-1beta-induced cell adhesion molecule expression in human umbilical vein endothelial cells.

作者信息

Yu Ya-Mei, Wang Zhi-Hong, Liu Chung-Hsien, Chen Chin-Seng

机构信息

Department of Nutrition, China Medical University, 91, Hsueh-Shih Road, Taichung, Taiwan.

出版信息

Br J Nutr. 2007 Apr;97(4):692-8. doi: 10.1017/S0007114507666409.

DOI:10.1017/S0007114507666409
PMID:17349082
Abstract

Expression of cell adhesion molecules by endothelium and the attachment of monocytes to endothelium may play a major role in atherosclerosis. Ellagic acid (EA) is a phenolic compound found in fruits and nuts including raspberries, strawberries, grapes and walnuts. Previous studies have indicated that EA possesses antioxidant activity in vitro. In the present study, we investigated the effects of EA on the formation of intracellular reactive oxygen species, the translocation of NFkappaB and expression of vascular cell adhesion molecule-1 (VCAM-1), intercellular adhesion molecule-1 and endothelial leucocyte adhesion molecule (E-selectin) induced by IL-1beta in human umbilical vein endothelial cells (HUVEC). We found that EA significantly reduced the binding of human monocytic cell line, U937, to IL-1beta-treated HUVEC. The production of reactive oxygen species by IL-1beta was dose-dependently suppressed by EA. Supplementation with increasing doses of EA up to 50 micromol/l was most effective in inhibiting the expression of VCAM-1 and E-selectin. Furthermore, the inhibition of IL-1beta-induced adhesion molecule expression by EA was manifested by the suppression of nuclear translocation of p65 and p50. In conclusion, EA inhibits IL-1beta-induced nuclear translocation of p65 and p50, thereby suppressing the expression of VCAM-1 and E-selectin, resulting in decreased monocyte adhesion. Thus, EA has anti-inflammatory properties and may play an important role in the prevention of atherosclerosis.

摘要

内皮细胞黏附分子的表达以及单核细胞与内皮细胞的黏附可能在动脉粥样硬化中起主要作用。鞣花酸(EA)是一种在树莓、草莓、葡萄和核桃等水果和坚果中发现的酚类化合物。先前的研究表明,EA在体外具有抗氧化活性。在本研究中,我们研究了EA对人脐静脉内皮细胞(HUVEC)中细胞内活性氧形成、NFκB易位以及白细胞介素-1β(IL-1β)诱导的血管细胞黏附分子-1(VCAM-1)、细胞间黏附分子-1和内皮白细胞黏附分子(E-选择素)表达的影响。我们发现EA显著减少了人单核细胞系U937与IL-1β处理的HUVEC的结合。EA剂量依赖性地抑制了IL-1β产生的活性氧。补充高达50 μmol/l的递增剂量EA在抑制VCAM-1和E-选择素的表达方面最有效。此外,EA对IL-1β诱导的黏附分子表达的抑制表现为p65和p50核易位的抑制。总之,EA抑制IL-1β诱导的p65和p50核易位,从而抑制VCAM-1和E-选择素的表达,导致单核细胞黏附减少。因此,EA具有抗炎特性,可能在动脉粥样硬化的预防中起重要作用。

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