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在离体灌注大鼠心脏中,重度和轻度缺氧期间冠状动脉血流与腺苷释放之间的关系,特别关注时间进程变化。

Relationship between coronary flow and adenosine release during severe and mild hypoxia in the isolated perfused rat heart with special reference to time-course change.

作者信息

Ishibashi T, Hara A, Abiko Y

机构信息

Department of Pharmacology, Niigata University School of Medicine, Japan.

出版信息

Heart Vessels. 1987;3(3):113-21. doi: 10.1007/BF02058786.

DOI:10.1007/BF02058786
PMID:3440778
Abstract

The contribution of endogenous adenosine to coronary vasodilation induced by global myocardial hypoxia was examined. In isolated rat hearts perfused by means of Langendorff's technique, the relationship between chronological changes in coronary flow and adenosine release during hypoxia was analyzed. The oxygenation level of myoglobin (MbO2), myocardial oxygen uptake, lactate release, and left ventricular pressure (LVP) was also measured. Adenosine was determined by radioimmunoassay, and the MbO2 levels by the optical method. Severe hypoxia (20% O2 + 75% N2 + 5% CO2) increased coronary flow, adenosine release, and lactate release and decreased both myocardial oxygen uptake and LVP. Mild hypoxia (50% O2 + 45% N2 + 5% CO2) also increased coronary flow, adenosine release, and lactate release, while it affected neither myocardial oxygen uptake nor LVP. These results suggest that the oxygen supply is compensated by an increase in coronary flow in mild hypoxia, whereas this does not occur in severe hypoxia. Changes in MbO2 were the reverse of those in coronary flow during severe hypoxia, confirming that a decrease in intracellular oxygen correlates well with an increase in coronary flow. The pattern of changes in adenosine release, however, was not identical with that in coronary flow in severe and mild hypoxia, indicating that there is no significant relationship between coronary flow and adenosine release in either severe or mild hypoxic hearts. These findings suggest that adenosine is not the only metabolic mediator of regulation of coronary flow in hypoxic hearts.

摘要

研究了内源性腺苷对整体心肌缺氧诱导的冠状动脉舒张的作用。在采用Langendorff技术灌注的离体大鼠心脏中,分析了缺氧期间冠状动脉血流的时间变化与腺苷释放之间的关系。还测量了肌红蛋白的氧合水平(MbO2)、心肌摄氧量、乳酸释放量和左心室压力(LVP)。腺苷通过放射免疫测定法测定,MbO2水平通过光学方法测定。严重缺氧(20% O2 + 75% N2 + 5% CO2)可增加冠状动脉血流、腺苷释放和乳酸释放,并降低心肌摄氧量和LVP。轻度缺氧(50% O2 + 45% N2 + 5% CO2)也可增加冠状动脉血流、腺苷释放和乳酸释放,而对心肌摄氧量和LVP均无影响。这些结果表明,在轻度缺氧时,冠状动脉血流增加可补偿氧供应,而在严重缺氧时则不会发生这种情况。在严重缺氧期间,MbO2的变化与冠状动脉血流的变化相反,证实细胞内氧的减少与冠状动脉血流的增加密切相关。然而,在严重和轻度缺氧时,腺苷释放的变化模式与冠状动脉血流的变化模式并不相同,表明在严重或轻度缺氧的心脏中,冠状动脉血流与腺苷释放之间没有显著关系。这些发现表明,腺苷不是缺氧心脏中调节冠状动脉血流的唯一代谢介质。

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本文引用的文献

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Cardiac nucleotides in hypoxia: possible role in regulation of coronary blood flow.缺氧时的心脏核苷酸:在冠状动脉血流调节中的可能作用。
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Coronary physiology.冠状动脉生理学
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