Tajima M, Katayose D, Bessho M, Isoyama S
First Department of Internal Medicine, Tohoku University School of Medicine, Sendai, Japan.
Cardiovasc Res. 1994 Mar;28(3):312-9. doi: 10.1093/cvr/28.3.312.
Myocardial adaptation has been reported to result from mild but chronic ischaemia in the hearts of patients with coronary artery disease. The aim of this study was to test the hypothesis that the responses of the chronically hypoxic myocardium to an episode of severe ischaemia, or the effects of acute ischaemic preconditioning on myocardial function after subsequent fatal ischaemia, may differ between the normoxic and the chronically hypoxic myocardium.
A rat model of three week hypoxia (10% O2) was used to simulate tissue hypoxia caused by chronic ischaemia. In isolated isovolumetrically contracting hearts perfused with oxygenated erythrocyte-containing Tyrode solution, systolic and diastolic functions during a 15 or 20 min period of ischaemia and reperfusion were measured in the normoxic control and chronically hypoxic groups.
Increases in diastolic pressure during ischaemia were smaller and the recovery of developed pressure during reperfusion was greater in the chronically hypoxic group than in the normoxic group. The hearts of the normoxic group never recovered from ischaemic damage after 20 min ischaemia. The beneficial effects of acute preconditioning with 5 min ischaemia on myocardial function were observed after 15 min ischaemia in the normoxic group, and during and after 20 min ischaemia in the chronically hypoxic group. Changes in lactate production and high energy phosphates could not explain the increased tolerance to ischaemia in the chronically hypoxic group.
Chronic hypoxia increased myocardial tolerance to ischaemia, and acute ischaemic preconditioning increased the tolerance further. Thus chronic hypoxia and acute ischaemic preconditioning independently activate protective mechanisms against ischaemia; the mechanisms may differ between the two types of insult.
据报道,冠状动脉疾病患者心脏中的轻度慢性缺血会导致心肌适应性改变。本研究的目的是检验以下假设:慢性缺氧心肌对严重缺血发作的反应,或急性缺血预处理对随后致命性缺血后心肌功能的影响,在常氧心肌和慢性缺氧心肌之间可能存在差异。
采用大鼠三周缺氧(10%氧气)模型来模拟慢性缺血引起的组织缺氧。在灌注含氧量红细胞的台氏液的离体等容收缩心脏中,测量常氧对照组和慢性缺氧组在缺血和再灌注15或20分钟期间的收缩和舒张功能。
与常氧组相比,慢性缺氧组缺血期间舒张压升高幅度较小,再灌注期间舒张末压恢复程度更大。常氧组心脏在缺血20分钟后从未从缺血损伤中恢复。常氧组在缺血15分钟后观察到5分钟缺血急性预处理对心肌功能的有益作用,而慢性缺氧组在缺血20分钟期间及之后观察到该作用。乳酸生成和高能磷酸化合物的变化无法解释慢性缺氧组对缺血耐受性的增加。
慢性缺氧增加了心肌对缺血的耐受性,急性缺血预处理进一步增加了耐受性。因此,慢性缺氧和急性缺血预处理独立激活了针对缺血的保护机制;两种损伤类型的机制可能不同。