Asimakis G K
University of Texas Medical Branch, Cardiothoracic Surgery, Galveston, USA.
J Mol Cell Cardiol. 1996 Mar;28(3):563-70. doi: 10.1006/jmcc.1996.0052.
The mechanism of ischemic preconditioning remains unknown. The role of glycogen depletion prior to prolonged ischemia was examined as a potential mechanism of ischemic preconditioning. The glycogen content of the rat heart varies in a 24-h rhythm. In a retrospective study, the relationships between the time of day the animals were sacrificed, pre-ischemic myocardial glycogen content, and post-ischemic functional recovery were assessed in non-conditioned and ischemically preconditioned hearts. The analyses were performed on previously published data (Asimakis et al.. 1992, 1993). After an equilibration perfusion, isolated rat hearts were given 40 min of global ischemia followed by 30 min of reperfusion. Preconditioned hearts received 5 min of ischemia followed by a 5-min recovery period prior to the 40-min ischemic period. Some of the hearts were freeze-clamped immediately prior to the 40-min ischemic period to determine pre-ischemic glycogen content. Pre-ischemic glycogen was higher in the morning than afternoon. The time of day correlated significantly with the pre-ischemic glycogen content of non-conditioned (r = 0.67; P < 0.005) and preconditioned (r = 0.79; P < 0.001) hearts. However, time of day did not correlate significantly with post-ischemic recovery of heart rate x developed pressure (HR x DP) on end-diastolic pressure (EDP) in either the non-conditioned or preconditioned hearts. The relationships were also assessed by subdividing the groups into either morning (a.m.) or afternoon (p.m.) hearts. The pre-ischemic glycogen content was lower in the non-conditioned-p.m. (n = 5) hearts compared to the non-conditioned-a.m. (n = 10) hearts (67.6 +/- 9.0 nu 128.1 +/- 13.3 nmol glucose/mg protein P < 0.005). However, there were no significant differences between p.m. (n = 13) and a.m. (n = 9) non-conditioned hearts with respect to post-ischemic recovery of HR x DP (20.6 +/- 4 nu 12.0 +/- 4% of baseline, respectively, P = N.S.). In contrast, preconditioned-p.m. (n = 6) and -a.m. (n = 7) had pre-ischemic glycogen contents of 49.6 +/- 6 and 76.6 +/- 5.0 nmol glucose/mg protein, respectively. These glycogen values were not significantly different from the non-conditioned-p.m. hearts (67.6 nmol/mg protein). However, post-ischemic recovery of HR x DP in the preconditioned-p.m. (n = 5) and -a.m. (n = 6) hearts were 54.6 +/- 5 and 51.4 +/- 8% of baseline, respectively (these values were significantly higher (P < 0.05) than the recovery for the non-conditioned-p.m. and -a.m. hearts). The results imply that the cardioprotection of ischemic preconditioning cannot be explained solely by myocardial glycogen depletion.
缺血预处理的机制尚不清楚。研究了长时间缺血前糖原耗竭作为缺血预处理潜在机制的作用。大鼠心脏的糖原含量呈24小时节律变化。在一项回顾性研究中,评估了在未预处理和经缺血预处理的心脏中,动物处死时间、缺血前心肌糖原含量与缺血后功能恢复之间的关系。分析是基于先前发表的数据(阿西马基斯等人,1992年、1993年)进行的。在平衡灌注后,对离体大鼠心脏进行40分钟的全心缺血,随后再灌注30分钟。预处理的心脏在40分钟缺血期之前先接受5分钟缺血,然后有5分钟的恢复期。一些心脏在40分钟缺血期之前立即进行冷冻钳夹,以测定缺血前糖原含量。缺血前糖原在上午高于下午。一天中的时间与未预处理心脏(r = 0.67;P < 0.005)和预处理心脏(r = 0.79;P < 0.001)的缺血前糖原含量显著相关。然而,无论是未预处理还是预处理的心脏,一天中的时间与缺血后心率×收缩压(HR×DP)相对于舒张末期压力(EDP)的恢复均无显著相关性。通过将各组再细分为上午(a.m.)或下午(p.m.)的心脏来评估这些关系。与未预处理上午组(n = 10)心脏相比,未预处理下午组(n = 5)心脏的缺血前糖原含量较低(67.6±9.0对128.1±13.3 nmol葡萄糖/毫克蛋白,P < 0.005)。然而,未预处理下午组(n = 13)和上午组(n = 9)心脏在缺血后HR×DP的恢复方面无显著差异(分别为基线的20.6±4对12.0±4%,P = 无显著性差异)。相比之下,预处理下午组(n = 6)和上午组(n = 7)的缺血前糖原含量分别为49.6±6和76.6±5.0 nmol葡萄糖/毫克蛋白。这些糖原值与未预处理下午组心脏(67.6 nmol/毫克蛋白)无显著差异。然而,预处理下午组(n = 5)和上午组(n = 6)心脏缺血后HR×DP的恢复分别为基线的54.6±5和51.4±8%(这些值显著高于(P < 0.05)未预处理下午组和上午组心脏的恢复)。结果表明,缺血预处理的心脏保护作用不能仅用心肌糖原耗竭来解释。