Suppr超能文献

钙可改善未成熟兔离体双心室工作心脏缺血后的机械功能和碳水化合物代谢。

Calcium improves mechanical function and carbohydrate metabolism following ischemia in isolated Bi-ventricular working hearts from immature rabbits.

作者信息

Itoi T, Lopaschuk G D

机构信息

Cardiovascular Disease Research Group, University of Alberta, Edmonton, Canada.

出版信息

J Mol Cell Cardiol. 1996 Jul;28(7):1501-14. doi: 10.1006/jmcc.1996.0140.

Abstract

In the adult heart an increase in extracellular [Ca2+] can contribute to the severity of ischemic injury. While experimental studies have suggested that the immature heart is more resistant to ischemia than the mature heart, the reasons for this are unclear. In this study, we determined the effects of increasing perfusate [Ca2+] from 1.25 to 2.5 mM on reperfusion recovery of mechanical function and energy substrate metabolism following ischemia. Isolated bi-ventricular working hearts from 2-week-old rabbits were subjected to a 55-min period of global ischemia followed by 40 min of aerobic reperfusion. Perfusate contained 11 mM glucose, 0.5 mM lactate, and 1.2 mM palmitate, containing either: (i) 1.25 mM Ca2+ throughout the perfusion period (n = 22), (ii) 1.25 mM Ca2+ prior to and during ischemia and 2.5 mM Ca2+ following ischemia (n = 19), or (iii) 2.5 mM Ca2+ throughout the perfusion period (n = 18). In hearts perfused with 1.25 mM Ca2+ throughout, a 57% recovery of preischemic function was seen following ischemia. If [Ca2+] was increased to 2.5 mM during reperfusion a significant improvement of function was seen (hearts recovered 127% of preischemic function). A concentration of 2.5 mM Ca2+ throughout the perfusion resulted in an increase in both pre- and post-ischemic function compared to hearts perfused with 1.25 mM Ca2+ throughout. In both experimental groups reperfused with 2.5 mM Ca2+ a greater than 200% increase in both glucose and lactate oxidation was seen during reperfusion. Fatty acid oxidation rates also returned to pre-ischemic levels in both groups reperfused with 2.5 mM Ca2+, while rates returned to only 53% in hearts reperfused with 1.25 mM Ca2+. As a result, increasing [Ca2+] from 1.25 to 2.5 mM resulted in a 100% increase in ATP production rates during reperfusion. In conclusion, this study demonstrates that increasing [Ca2+] significantly improves post-ischemic recovery of function in isolated bi-ventricular working immature rabbit hearts subjected to a 55-min period of ischemia. The beneficial effects of Ca2+ in these immature hearts may be due to both a direct inotropic effect and a marked increase in carbohydrate oxidation and ATP production during reperfusion.

摘要

在成年心脏中,细胞外[Ca2+]的增加会加重缺血性损伤的严重程度。虽然实验研究表明未成熟心脏比成熟心脏对缺血更具抵抗力,但其原因尚不清楚。在本研究中,我们测定了将灌注液[Ca2+]从1.25 mM增加到2.5 mM对缺血后机械功能和能量底物代谢再灌注恢复的影响。从2周龄兔子分离的双心室工作心脏经历55分钟的全心缺血,随后进行40分钟的有氧再灌注。灌注液含有11 mM葡萄糖、0.5 mM乳酸和1.2 mM棕榈酸,分为以下三组:(i) 在整个灌注期含有1.25 mM Ca2+(n = 22);(ii) 在缺血前和缺血期间含有1.25 mM Ca2+,缺血后含有2.5 mM Ca2+(n = 19);或(iii) 在整个灌注期含有2.5 mM Ca2+(n = 18)。在整个过程中用1.25 mM Ca2+灌注的心脏,缺血后缺血前功能恢复了57%。如果在再灌注期间将[Ca2+]增加到2.5 mM,则功能有显著改善(心脏恢复到缺血前功能的127%)。与整个过程用1.25 mM Ca2+灌注的心脏相比,整个灌注期2.5 mM Ca2+的浓度导致缺血前后功能均增加。在两个用2.5 mM Ca2+再灌注的实验组中,再灌注期间葡萄糖和乳酸氧化均增加了200%以上。在两个用2.5 mM Ca2+再灌注的组中,脂肪酸氧化率也恢复到缺血前水平,而在1.25 mM Ca2+再灌注的心脏中,脂肪酸氧化率仅恢复到53%。因此,将[Ca2+]从1.25 mM增加到2.5 mM导致再灌注期间ATP产生率增加100%。总之,本研究表明,将[Ca2+]增加可显著改善经历55分钟缺血的分离双心室工作未成熟兔心脏缺血后的功能恢复。Ca2+在这些未成熟心脏中的有益作用可能归因于直接的正性肌力作用以及再灌注期间碳水化合物氧化和ATP产生的显著增加。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验