首页> 外文OA文献 >Demonstration of free radical generation in the 'stunned' myocardium in the conscious dog and identification of major differences between conscious and open-chest dogs.
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Demonstration of free radical generation in the 'stunned' myocardium in the conscious dog and identification of major differences between conscious and open-chest dogs.

机译:有意识的狗的“震惊的”心肌中自由基生成的证明,以及有意识的和开胸的狗之间主要差异的鉴定。

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摘要

Conscious dogs undergoing a 15-min coronary occlusion were given alpha-phenyl N-tert-butyl nitrone (PBN) and the local coronary venous plasma was analyzed by electron paramagnetic resonance spectroscopy. A prolonged myocardial release of PBN radical adducts was observed, which exhibited a burst in the initial minutes of reflow (peaking at 3 min) and then abated but continued for 1-3 h after reperfusion. Computer simulation revealed the presence of at least two PBN adducts (aN = 15.2 G and a beta H = 6.0 G; aN = 14.6 G and a beta H = 3.0 G), both consistent with the trapping of secondary carbon-centered radicals. No appreciable PBN adduct production was observed when collateral flow exceeded 30-40% of nonischemic flow, indicating that a flow reduction of at least 60% is necessary to trigger free radical reactions. There was a direct relationship between the magnitude of PBN adduct production and the severity of contractile dysfunction (r = 0.77), suggesting that the radicals generated upon reperfusion play a causal role in the subsequent stunning. The total release of PBN adducts after 3 h of reperfusion following a 15-min coronary occlusion was found to be approximately five times greater in open-chest compared with conscious dogs; at the same time, the recovery of wall thickening was markedly less in open-chest dogs. This study represents the first application of spin trapping to a conscious animal model of myocardial ischemia. The results demonstrate (a) that free radicals are generated in the stunned myocardium in the absence of the artificial or abnormal conditions associated with previously used models (isolated hearts, open-chest preparations), and (b) that both the severity of postischemic dysfunction and the magnitude of the attendant free radical production are greatly exaggerated in the open-chest dog, implying that previous conclusions derived from this model may not be applicable to conscious animals or to humans. This investigation also provides a method to measure free radicals in awake animals.
机译:给有意识的狗进行15分钟的冠状动脉闭塞,给予α-苯基N-叔丁基硝酮(PBN),并通过电子顺磁共振波谱分析局部冠状静脉血浆。观察到PBN自由基加合物的心肌延长释放,其在回流的最初几分钟(在3分钟达到峰值)表现出爆发,然后减弱,但在再灌注后持续1-3小时。计算机模拟显示,存在至少两个PBN加合物(aN = 15.2 G和beta H = 6.0 G; aN = 14.6 G和beta H = 3.0 G),两者均与次级碳中心自由基的俘获一致。当侧支血流超过非缺血血流的30-40%时,未观察到明显的PBN加合物生成,表明触发自由基反应所需的血流减少至少60%。 PBN加合物的产生量与收缩功能障碍的严重程度之间存在直接关系(r = 0.77),表明再灌注时产生的自由基在随后的击晕中起因果作用。发现在15分钟的冠状动脉闭塞后再灌注3小时后,PBN加合物的总释放量比有意识的犬高约5倍。同时,开胸犬的壁增厚恢复明显减少。这项研究代表了自旋捕获技术在心肌缺血的自觉动物模型中的首次应用。结果表明:(a)在没有与以前使用的模型(离体心脏,开胸准备)相关的人工或异常条件的情况下,在震惊的心肌中会产生自由基;(b)缺血后功能障碍的严重程度敞开的狗极大地夸大了随之而来的自由基的产生量,这暗示从该模型得出的先前结论可能不适用于有意识的动物或人类。这项研究还提供了一种方法来测量清醒动物中的自由基。

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