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反式石竹烯(TC)对白细胞与内皮细胞黏附的抑制作用。

Inhibitory effect of trans-caryophyllene (TC) on leukocyte-endothelial attachment.

作者信息

Zhang Zhen, Yang Chunfeng, Dai Xinlun, Ao Yu, Li Yumei

机构信息

Department of Pediatric ICU, The First Affiliated Hospital of Jilin University, Changchun 130021, Jilin, China.

Clinical Medical College, The First Affiliated Hospital of Jilin University, Changchun 130021, Jilin, China.

出版信息

Toxicol Appl Pharmacol. 2017 Aug 15;329:326-333. doi: 10.1016/j.taap.2017.06.016. Epub 2017 Jun 15.

Abstract

trans-Caryophyllene (TC) is a major component found in the essential oils of many spices and foods/medicinal plants. It is a natural sesquiterpene and has been the subject of numerous studies. However, the effects of TC on vascular inflammation remain unknown. In this study, we reported that TC treatment in human umbilical vein endothelial cells (HUVECs) prevented attachment of monocytic leukemia cell line THP-1 cells to endothelial cells. In addition, in vivo results indicate that TC inhibited macrophage infiltration to the aortic surface and reduced total serum levels of cholesterol and triglycerides. Importantly, administration of TC could inhibit the induction of vascular cell adhesion molecule-1 (VCAM-1) both in vitro and in vivo. Notably, our data indicate that the inhibitory effects of TC on the expression of VCAM-1 are mediated by the JAK2/STAT1/IRF-1 pathway. TC is a specific agonist of the type 2 cannabinoid receptor (CB2R). Importantly, we further verified that the inhibitory effects of TC on the expression of IRF-1 and VCAM-1 are dependent on activation of CB2R. Inhibition of CB2R by either specific inhibitors or RNA interference abolished the inhibitory effects of TC on the expression of IRF-1 and VCAM-1. Our results suggest that TC might have a capacity to suppress the development of atherosclerosis.

摘要

反式石竹烯(TC)是许多香料、食品/药用植物精油中的主要成分。它是一种天然倍半萜烯,已成为众多研究的对象。然而,TC对血管炎症的影响尚不清楚。在本研究中,我们报道了在人脐静脉内皮细胞(HUVECs)中进行TC处理可阻止单核细胞白血病细胞系THP-1细胞与内皮细胞的附着。此外,体内结果表明,TC可抑制巨噬细胞向主动脉表面浸润,并降低血清总胆固醇和甘油三酯水平。重要的是,给予TC在体外和体内均可抑制血管细胞黏附分子-1(VCAM-1)的诱导。值得注意的是,我们的数据表明,TC对VCAM-1表达的抑制作用是由JAK2/STAT1/IRF-1途径介导的。TC是2型大麻素受体(CB2R)的特异性激动剂。重要的是,我们进一步证实,TC对IRF-1和VCAM-1表达的抑制作用依赖于CB2R的激活。用特异性抑制剂或RNA干扰抑制CB2R可消除TC对IRF-1和VCAM-1表达的抑制作用。我们的结果表明,TC可能具有抑制动脉粥样硬化发展的能力。

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