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环氧化酶-2在人类动脉粥样硬化颈动脉中的表达。

Expression of cyclo-oxygenase-2 in human atherosclerotic carotid arteries.

作者信息

Stemme V, Swedenborg J, Claesson H, Hansson G K

机构信息

Cardiovascular Research Unit, Center for Molecular Medicine, Stockholm, Sweden.

出版信息

Eur J Vasc Endovasc Surg. 2000 Aug;20(2):146-52. doi: 10.1053/ejvs.2000.1145.

Abstract

OBJECTIVES

the preventive effect of acetylsalicylic acid in cardiovascular disease may be due to inhibition of platelet aggregation mediated by COX-1, but may in addition be due to anti-inflammatory effects by inhibition of COX-2. The objective of this study was to analyse the expression of COX-1 and COX-2 in atherosclerotic and healthy vascular walls.

DESIGN

the expression COX-1 and COX-2 was analysed in biopsies from human atherosclerotic carotid arteries and from healthy mammary arteries and saphenous veins.

MATERIALS

vascular biopsies were obtained from patients undergoing carotid endarterectomy or coronary bypass surgery.

METHODS

RT-PCR was used for mRNA analysis and for localization of proteins we used immunohistochemistry.

RESULTS

COX-2 was found in atherosclerotic plaques: in macrophages, in some smooth muscle cells and in endothelial cells of small vessels in the lesions. In non-atherosclerotic blood vessels, COX-2 was detected in the endothelium of the vasa vasorum in the adventitia. COX-1 was found in the endothelium in healthy and in atherosclerotic vessels.

CONCLUSIONS

the expression of COX-2 by inflammatory and vascular cells in atherosclerotic arteries suggests that products of this enzyme may be important in the pathogenesis of atherosclerosis.

摘要

目的

乙酰水杨酸对心血管疾病的预防作用可能归因于其对COX - 1介导的血小板聚集的抑制作用,但也可能归因于其通过抑制COX - 2产生的抗炎作用。本研究的目的是分析COX - 1和COX - 2在动脉粥样硬化血管壁和健康血管壁中的表达情况。

设计

分析从人类动脉粥样硬化颈动脉以及健康乳腺动脉和大隐静脉活检组织中COX - 1和COX - 2的表达。

材料

血管活检组织取自接受颈动脉内膜切除术或冠状动脉搭桥手术的患者。

方法

采用逆转录聚合酶链反应(RT - PCR)进行mRNA分析,并用免疫组织化学方法定位蛋白质。

结果

在动脉粥样硬化斑块中发现了COX - 2:在病变部位的巨噬细胞、一些平滑肌细胞和小血管内皮细胞中。在非动脉粥样硬化血管中,在外膜的血管滋养管内皮中检测到COX - 2。在健康血管和动脉粥样硬化血管的内皮中均发现了COX - 1。

结论

动脉粥样硬化动脉中炎症细胞和血管细胞表达COX - 2表明该酶的产物可能在动脉粥样硬化的发病机制中起重要作用。

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