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预处理在离体大鼠心脏中是通过糖原耗竭起作用的吗?

Does preconditioning act by glycogen depletion in the isolated rat heart?

作者信息

King L M, Opie L H

机构信息

MRC/UCT Ischaemic Heart Disease Research Unit, UCT Medical School, Observatory, Cape Town, South Africa.

出版信息

J Mol Cell Cardiol. 1996 Dec;28(12):2305-21. doi: 10.1006/jmcc.1996.0224.

Abstract

Preconditioning hastens the time to onset of ischaemic contracture and increases peak contracture in an isolated perfused rat heart, but improves recovery of function. The preconditioning ischaemic episode is also known to deplete glycogen stores. We tested whether a depletion in glycogen is related to the protection conferred by preconditioning. The isolated Langendorff perfused rat heart, with a left ventricular balloon to record function, was perfused with either glucose 11 mM, acetate 5 mM, or glucose 11 mM + insulin to alter pre-ischaemic glycogen levels prior to 30 min total global ischaemia. In addition, hearts were preconditioned by an episode of 5 min ischaemia and 5 min reperfusion. Time to onset of contracture (TOC-min), peak contracture and recovery of developed pressure after 20 min reperfusion with glucose-containing perfusate (both expressed as percentage pre-ischaemic developed pressure) were measured (n = 9-10). Parallel groups of hearts were clamped at various times for assessment of tissue metabolites. Acetate pre-perfusion reduced glycogen levels compared to glucose hearts, from 16.27 +/- 0.44 to 10.77 +/- 0.96 mumol/g wet wt. TOC was reduced and peak contracture increased, with poor functional recovery. Glucose + insulin pre-perfusion increased glycogen (21.39 +/- 1.08 mumol/g wet wt) with opposite effects on contracture, but functional recovery was still poor. Preconditioning hastened the time to onset of contracture, which could be partially attributed to glycogen depletion. Preconditioning significantly improved functional recovery in glucose hearts, but had little or no effect in the other groups. Thus the protective effect on functional recovery could not be linked to glycogen depletion. Pre-ischaemic glycogen appeared to play a dual role. When low, preconditioning was ineffective, presumably because of lack of production of glycolytic ATP, and severe contracture. When pre-ischaemic glycogen was increased, preconditioning was also relatively ineffective, presumably because of excess accumulation of the metabolites of glycogenolysis.

摘要

预处理可缩短缺血性挛缩的发生时间,并增加离体灌注大鼠心脏的挛缩峰值,但能改善功能恢复。已知预处理的缺血期也会消耗糖原储备。我们测试了糖原耗竭是否与预处理所赋予的保护作用有关。将带有左心室球囊以记录功能的离体Langendorff灌注大鼠心脏,用11 mM葡萄糖、5 mM乙酸盐或11 mM葡萄糖 + 胰岛素进行灌注,以在30分钟全心缺血前改变缺血前的糖原水平。此外,心脏通过5分钟缺血和5分钟再灌注进行预处理。测量挛缩发生时间(TOC - 分钟)、挛缩峰值以及在含葡萄糖灌注液再灌注20分钟后舒张期压力的恢复情况(均以缺血前舒张期压力的百分比表示)(n = 9 - 10)。在不同时间对平行组的心脏进行钳夹以评估组织代谢物。与葡萄糖灌注的心脏相比,乙酸盐预灌注降低了糖原水平,从16.27±0.44降至10.77±0.96 μmol/g湿重。TOC缩短,挛缩峰值增加,功能恢复较差。葡萄糖 + 胰岛素预灌注增加了糖原(21.39±1.08 μmol/g湿重),对挛缩有相反的影响,但功能恢复仍然较差。预处理加快了挛缩发生时间,这可能部分归因于糖原耗竭。预处理显著改善了葡萄糖灌注心脏的功能恢复,但对其他组几乎没有影响。因此,对功能恢复的保护作用与糖原耗竭无关。缺血前糖原似乎起双重作用。当含量低时,预处理无效,可能是因为缺乏糖酵解ATP的产生以及严重挛缩。当缺血前糖原增加时,预处理也相对无效,可能是因为糖原分解代谢物的过度积累。

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