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正常犬血小板环氧化酶的表达。

Platelet cyclooxygenase expression in normal dogs.

机构信息

Department of Clinical Sciences, Mississippi State University, Mississippi State, MS 39762-6100, USA.

出版信息

J Vet Intern Med. 2011 Sep-Oct;25(5):1106-12. doi: 10.1111/j.1939-1676.2011.00781.x. Epub 2011 Aug 30.

Abstract

BACKGROUND

Human platelets express both cyclooxygenase-1 (COX-1) and cyclooxygenase-2 (COX-2). Variation in COX-2 expression could be a mechanism for variable response to aspirin.

HYPOTHESIS/OBJECTIVES: The hypotheses were that circulating canine platelets express COX-1 and COX-2, and that aspirin alters COX expression. The objective was to identify changes in platelet COX expression and in platelet function caused by aspirin administration to dogs.

ANIMALS

Eight female, intact hounds.

METHODS

A single population, repeated measures design was used to evaluate platelet COX-1 and COX-2 expression by flow cytometry before and after aspirin (10 mg/kg Q12h for 10 days). Platelet function was analyzed via PFA-100(®) (collagen/epinephrine), and urine 11-dehydro-thromboxane B(2) (11-dTXB(2)) was measured and normalized to urinary creatinine. Differences in COX expression, PFA-100(®) closure times, and urine 11-dTXB(2 ): creatinine ratio were analyzed before and after aspirin administration.

RESULTS

Both COX-1 and COX-2 were expressed in canine platelets. COX-1 mean fluorescent intensity (MFI) increased in all dogs, by 250% (range 63-476%), while COX-2 expression did not change significantly (P = 0.124) after aspirin exposure, with large interindividual variation. PFA-100(®) closure times were prolonged and urine 11-dTXB(2) concentration decreased in all dogs after aspirin administration.

CONCLUSIONS AND CLINICAL IMPORTANCE

Canine platelets express both COX isoforms. After aspirin exposure, COX-1 expression increased despite impairment of platelet function, while COX-2 expression varied markedly among dogs. Variability in platelet COX-2 expression should be explored as a potential mechanism for, or marker of, variable aspirin responsiveness.

摘要

背景

人类血小板表达环氧化酶-1(COX-1)和环氧化酶-2(COX-2)。COX-2 表达的变化可能是阿司匹林反应性差异的机制。

假设/目的:假设循环犬血小板表达 COX-1 和 COX-2,并且阿司匹林改变 COX 表达。目的是确定阿司匹林给药对犬血小板 COX 表达和血小板功能的变化。

动物

8 只雌性,完整的猎犬。

方法

采用单一群体、重复测量设计,在阿司匹林(10mg/kg,Q12h,共 10 天)前后通过流式细胞术评估血小板 COX-1 和 COX-2 的表达。通过 PFA-100(®)(胶原/肾上腺素)分析血小板功能,并测量尿 11-脱氢血栓素 B(2)(11-dTXB(2))并归一化为尿肌酐。分析阿司匹林给药前后 COX 表达、PFA-100(®)闭合时间和尿 11-dTXB(2):肌酐比值的差异。

结果

犬血小板均表达 COX-1 和 COX-2。阿司匹林暴露后,所有犬的 COX-1 平均荧光强度(MFI)均增加,增加 250%(范围 63-476%),而 COX-2 表达无明显变化(P=0.124),个体间差异较大。所有犬的 PFA-100(®)闭合时间延长,尿 11-dTXB(2)浓度降低。

结论和临床意义

犬血小板表达两种 COX 同工酶。阿司匹林暴露后,尽管血小板功能受损,COX-1 表达增加,而 COX-2 表达在犬之间差异较大。血小板 COX-2 表达的变异性应作为阿司匹林反应性差异的潜在机制或标志物进行探讨。

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