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过氧化低密度脂蛋白在人体起搏诱导缺血期间心肌血栓素合成中的决定性作用。

Determinative role of peroxidized low-density lipoprotein in myocardial thromboxane synthesis during pacing-induced ischaemia in humans.

作者信息

Hsu H C, Chen M F, Lee C M, Lee Y T

机构信息

Department of Internal Medicine (Cardiology), National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Clin Sci (Lond). 1998 Jan;94(1):29-34. doi: 10.1042/cs0940029.

Abstract
  1. Myocardial thromboxane A2 production increases in patients with pacing-induced ischaemia and correlates with a decrease in myocardial lactate extraction. The release of myocardial thromboxane A2 before any lactate production was observed in patients with unstable angina. This study was proposed to clarify whether the early thromboxane A2 release contributed to the ongoing myocardial ischaemia and to determine which metabolites can be attributed to the thromboxane A2 release. Thirty-five patients with chest pain and positive treadmill exercise test underwent atrial pacing to the predicted maximal heart rate. The pacing was maintained at this peak rate for 10 min, then ceased. Blood samples of the ascending aorta and coronary sinus were drawn simultaneously at rest, at 2 and 10 min of peak-pacing, and 5 and 10 min after termination of the pacing; samples were used for analyses of lipid profiles, prostacyclin, thromboxane A2, lactate and lipid peroxides on plasma and low-density lipoprotein particles. 2. Twenty out of 35 patients who displayed pacing-induced ischaemia were documented by electrocardiographic evidence of ST depression > 2 mm developing after 2 min of peak-pacing [ischaemic group, ST delta(+)]. They had (i) negative fractional lactate extraction; (ii) pacing-induced decreases of plasma thromboxane A2 levels in the coronary sinus blood (564 +/- 57 versus 479 +/- 47 ng/l, P < 0.05) at 2 min of peak-pacing; the data increased at 10 min of peak-pacing (564 +/- 57 versus 620 +/- 60 ng/l, P < 0.05), then returned to baseline levels at 5 and 10 min post-pacing; (iii) significantly increased lipid peroxides on low-density lipoprotein of the coronary sinus blood at 2 and 10 min of peak-pacing (each P < 0.001), as well as at 5 min post-pacing (P < 0.05); (iv) significant correlation between thromboxane A2 levels and lipid peroxides on low-density lipoprotein of the coronary sinus blood samples. 3. In ST delta(+) patients, myocardial thromboxane synthesis changed before lactate production and correlated with the increase of lipid peroxides on low-density lipoprotein of the coronary venous blood. This implies that lipid peroxides on low-density lipoprotein participate in thromboxane production and play a determinative role in pacing-induced ischaemia.
摘要
  1. 起搏诱导性缺血患者的心肌血栓素A2生成增加,且与心肌乳酸摄取减少相关。在不稳定型心绞痛患者中,在观察到任何乳酸生成之前就有心肌血栓素A2的释放。本研究旨在阐明早期血栓素A2释放是否促成了持续的心肌缺血,并确定哪些代谢产物可归因于血栓素A2的释放。35例胸痛且平板运动试验阳性的患者接受心房起搏至预测的最大心率。起搏以该峰值速率维持10分钟,然后停止。在静息时、起搏峰值的2分钟和10分钟以及起搏终止后的5分钟和10分钟同时采集升主动脉和冠状窦的血样;样本用于分析血浆和低密度脂蛋白颗粒上的脂质谱、前列环素、血栓素A2、乳酸和脂质过氧化物。2. 35例出现起搏诱导性缺血的患者中,20例通过起搏峰值2分钟后ST段压低>2mm的心电图证据得以记录[缺血组,STδ(+)]。他们有:(i) 乳酸摄取分数为负;(ii) 起搏峰值2分钟时冠状窦血中血浆血栓素A2水平的起搏诱导性降低(564±57对479±47ng/l,P<0.05);数据在起搏峰值10分钟时增加(564±57对620±60ng/l,P<0.05),然后在起搏后5分钟和10分钟恢复到基线水平;(iii) 起搏峰值2分钟和10分钟时以及起搏后5分钟冠状窦血低密度脂蛋白上的脂质过氧化物显著增加(各P<0.001);(iv) 冠状窦血样本中血栓素A2水平与低密度脂蛋白上的脂质过氧化物之间存在显著相关性。3. 在STδ(+)患者中,心肌血栓素合成在乳酸生成之前发生变化,并与冠状静脉血低密度脂蛋白上脂质过氧化物的增加相关。这意味着低密度脂蛋白上的脂质过氧化物参与血栓素生成,并在起搏诱导性缺血中起决定性作用。

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