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血小板碳酸酐酶 II,一种被遗忘的酶,可能是导致阿司匹林抵抗的原因。

Platelet Carbonic Anhydrase II, a Forgotten Enzyme, May Be Responsible for Aspirin Resistance.

机构信息

Department of Internal Medicine, Occupational Diseases and Hypertension, Wroclaw Medical University, Wroclaw, Poland.

Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Warszawa, Poland.

出版信息

Oxid Med Cell Longev. 2017;2017:3132063. doi: 10.1155/2017/3132063. Epub 2017 Sep 27.

Abstract

BACKGROUND

Thromboembolic events constitute a major health problem, despite the steadily expanding arsenal of antiplatelet drugs. Hence, there is still a need to optimize the antiplatelet therapy.

OBJECTIVES

The aim of our study was to verify a hypothesis that there are no differences in platelet proteome between two groups of healthy people representing different acetylsalicylic acid (aspirin) responses as assessed by the liquid chromatography/mass spectrometry (LC/MS) technique.

PATIENTS/METHODS: A total of 61 healthy volunteers were recruited for the study. Physical examination and blood collection were followed by platelet-rich plasma aggregation assays and platelet separation for proteomic LC/MS analysis. Arachidonic acid- (AA-) induced aggregation (in the presence of aspirin) allowed to divide study participants into two groups aspirin-resistant (AR) and aspirin-sensitive (AS) ones. Subsequently, platelet proteome was compared in groups using the LC/MS analysis.

RESULTS

The LC/MS analysis of platelet proteome between groups revealed that out of all identified proteins, the only discriminatory protein, affecting aspirin responsiveness, is platelet carbonic anhydrase II (CA II).

CONCLUSIONS

CA II is a platelet function modulator and should be taken into consideration as a cardiovascular event risk factor or therapeutic target.

摘要

背景

尽管抗血小板药物不断增加,但血栓栓塞事件仍是一个主要的健康问题。因此,仍然需要优化抗血小板治疗。

目的

我们的研究旨在验证一个假设,即通过液相色谱/质谱(LC/MS)技术评估,两组健康人群的血小板蛋白质组之间没有差异,这两组人群代表不同的乙酰水杨酸(阿司匹林)反应。

患者/方法:共招募了 61 名健康志愿者进行研究。进行体格检查和采血后,进行富含血小板的血浆聚集试验和用于蛋白质组学 LC/MS 分析的血小板分离。在存在阿司匹林的情况下,花生四烯酸(AA)诱导的聚集允许将研究参与者分为阿司匹林抵抗(AR)和阿司匹林敏感(AS)两组。然后,使用 LC/MS 分析比较两组的血小板蛋白质组。

结果

对两组之间的血小板蛋白质组进行 LC/MS 分析显示,在所有鉴定的蛋白质中,唯一具有区分性的、影响阿司匹林反应性的蛋白质是血小板碳酸酐酶 II(CA II)。

结论

CA II 是血小板功能调节剂,应将其视为心血管事件的风险因素或治疗靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2768/5635279/e81aa99e1ac9/OMCL2017-3132063.001.jpg

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