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丙酸盐通过抑制核因子-κB(NF-κB)激活来降低细胞因子诱导的血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-1(ICAM-1)的表达。

Propionate reduces the cytokine-induced VCAM-1 and ICAM-1 expression by inhibiting nuclear factor-kappa B (NF-kappaB) activation.

作者信息

Zapolska-Downar D, Naruszewicz M

机构信息

Department of Biochemistry and Clinical Chemistry, The Warsaw Medical University, Banacha 1 Street, Warsaw, Poland.

出版信息

J Physiol Pharmacol. 2009 Jun;60(2):123-31.

Abstract

Adhesion and migration of leukocytes into the surrounding tissue are crucial steps in inflammation, immunity and atherogenesis. Expression of cell adhesion molecules by endothelial cells plays a role in these processes. Propionate is a naturally occurring short chain fatty acid produced by bacterial fermentation of dietary fibre. High intake of dietary fibre has been associated with an improved bowel function and with a reduced risk of cardiovascular disease. However, the molecular mechanisms responsible for these effects remain unknown. In this study, the effects of propionate on the expression of endothelial leukocyte adhesion molecules by cytokine-stimulated human umbilical vein endothelial cells (HUVEC) were investigated. Pretreatment of HUVEC with propionate significantly inhibited the tumor necrosis factor alpha (TNF-alpha)-induced expression of vascular cell adhesion molecule-1 (VCAM-1) and intracellular adhesion molecule-1 (ICAM-1) in a time- and dose-dependent manner. At 10 mM, propionate also inhibited the interleukin-1 (IL- 1)-mediated VCAM-1 and ICAM-1 expression, with the latter effect being more pronounced, as well as decreased the TNF-alpha-induced VCAM-1 and ICAM-1 mRNA expression in a similar manner. The decrease in VCAM-1 and ICAM-1 expression was associated with a reduction of adherence of monocytes and lymphocytes to the cytokine-stimulated HUVEC. In addition, propionate significantly inhibited the TNF-alpha-induced activation of nuclear factor-kappa B (NF-kappaB) and significantly increased the expression of peroxisome proliferator-activated receptor alpha (PPARalpha) in HUVEC. These results demonstrate that propionate may have antiinflammatory and possibly antiatherogenic properties. Our findings warrant further investigation into the therapeutic effects of propionate on a number of pathological events nvolving leukocyte recruitment.

摘要

白细胞黏附并迁移至周围组织是炎症、免疫及动脉粥样硬化形成过程中的关键步骤。内皮细胞表达细胞黏附分子在这些过程中发挥作用。丙酸是膳食纤维经细菌发酵产生的一种天然存在的短链脂肪酸。高膳食纤维摄入与肠道功能改善及心血管疾病风险降低相关。然而,导致这些效应的分子机制仍不清楚。在本研究中,我们调查了丙酸对细胞因子刺激的人脐静脉内皮细胞(HUVEC)表达内皮白细胞黏附分子的影响。用丙酸预处理HUVEC可显著抑制肿瘤坏死因子α(TNF-α)诱导的血管细胞黏附分子-1(VCAM-1)和细胞间黏附分子-1(ICAM-1)的表达,且呈时间和剂量依赖性。在10 mM时,丙酸还抑制白细胞介素-1(IL-1)介导的VCAM-1和ICAM-1表达,对后者的作用更明显,同时以类似方式降低TNF-α诱导的VCAM-1和ICAM-1 mRNA表达。VCAM-1和ICAM-1表达的降低与单核细胞和淋巴细胞对细胞因子刺激的HUVEC黏附减少相关。此外,丙酸显著抑制TNF-α诱导的核因子κB(NF-κB)激活,并显著增加HUVEC中过氧化物酶体增殖物激活受体α(PPARα)的表达。这些结果表明,丙酸可能具有抗炎及可能的抗动脉粥样硬化特性。我们的发现值得进一步研究丙酸对涉及白细胞募集的多种病理事件的治疗作用。

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