Lochner A, Marais E, Genade S, Huisamen B, du Toit E F, Moolman J A
Department of Biomedical Sciences (Section Medical Physiology), Faculty of Health Sciences, University of Stellenbosch, Stellenbosch.
Cardiovasc J Afr. 2009 Jan-Feb;20(1):43-51.
Exposure of the heart to one or more short episodes of ischaemia/reperfusion protects the heart against a subsequent prolonged period of ischaemia, as evidenced by a reduction in infarct size and an improvement in functional recovery during reperfusion. Elucidation of the mechanism of this endogenous protection could lead to the development of pharmacological mimetics to be used in the clinical setting. The aim of our studies was therefore to gain more information regarding the mechanism of ischaemic preconditioning, using the isolated perfused working rat heart as model. A preconditioning protocol of 1 x 5 or 3 x 5 min of ischaemia, interspersed with 5 min of reperfusion was found to protect hearts exposed to 25 min of global ischaemia or 35-45 min of regional ischaemia. These models were used throughout our studies. In view of the release of catecholamines by ischaemic tissue, our first aim was to evaluate the role of the alphaadrenergic receptor in ischaemic preconditioning. However, using a multi-cycle ischaemic preconditioning protocol, we could not find any evidence for alpha-1 adrenergic or PKC activation in the mechanism of preconditioning. Cyclic increases in the tissue cyclic nucleotides, cAMP and cGMP were found, however, to occur during a multi-cycle preconditioning protocol, suggesting roles for the beta-adrenergic signalling pathway and nitric oxide (NO) as triggers of cardioprotection. This was substantiated by the findings that (1) administration of the beta-adrenergic agonist, isoproterenol, or the NO donors SNAP or SNP before sustained ischaemia also elicited cardioprotection similar to ischaemic preconditioning; (2) beta-adrenergic blockade or nitric oxide synthase inhibition during an ischaemic preconditioning protocol abolished protection. Effectors downstream of cAMP, such as p38MAPK and CREB, were also demonstrated to be involved in the triggering process. Our next step was to evaluate intracellular signalling during sustained ischaemia and reperfusion. Our results showed that ischaemic preconditioned-induced cardioprotection was associated with a significant reduction in tissue cAMP, attenuation of p38MAPK activation and increased tissue cGMP levels and HSP27 activation, compared to non-preconditioned hearts. The role of the stress kinase p38MAPK was further investigated by using the inhibitor SB203580. Our results suggested that injury by necrosis and apoptosis share activation of p38MAPK as a common signal transduction pathway and that pharmacological targeting of this kinase offers a tenable option to manipulate both these processes during ischaemia/reperfusion injury.
心脏经历一次或多次短暂的缺血/再灌注可保护心脏免受随后长时间缺血的影响,这表现为梗死面积减小以及再灌注期间功能恢复得到改善。阐明这种内源性保护机制可能会促使开发出可用于临床的药理学模拟物。因此,我们研究的目的是利用离体灌注的工作大鼠心脏作为模型,获取更多关于缺血预处理机制的信息。发现1×5分钟或3×5分钟缺血并穿插5分钟再灌注的预处理方案可保护心脏免受25分钟全心缺血或35 - 45分钟局部缺血的影响。在我们的整个研究中都使用了这些模型。鉴于缺血组织会释放儿茶酚胺,我们的首要目标是评估α - 肾上腺素能受体在缺血预处理中的作用。然而,使用多周期缺血预处理方案时,我们在预处理机制中未发现任何α - 1肾上腺素能或蛋白激酶C(PKC)激活的证据。不过,在多周期预处理方案中发现组织环核苷酸cAMP和cGMP呈周期性增加,这表明β - 肾上腺素能信号通路和一氧化氮(NO)作为心脏保护触发因素发挥了作用。以下发现证实了这一点:(1)在持续缺血前给予β - 肾上腺素能激动剂异丙肾上腺素或NO供体硝普钠(SNAP)或亚硝基铁氰化钠(SNP)也能引发与缺血预处理类似的心脏保护作用;(2)在缺血预处理方案期间进行β - 肾上腺素能阻断或一氧化氮合酶抑制会消除保护作用。还证明了cAMP下游的效应器,如p38丝裂原活化蛋白激酶(p38MAPK)和环磷腺苷反应元件结合蛋白(CREB)也参与了触发过程。我们的下一步是评估持续缺血和再灌注期间的细胞内信号传导。我们的结果表明,与未预处理的心脏相比,缺血预处理诱导的心脏保护作用与组织cAMP显著降低、p38MAPK激活减弱以及组织cGMP水平升高和热休克蛋白27(HSP27)激活有关。通过使用抑制剂SB203580进一步研究了应激激酶p38MAPK的作用。我们的结果表明,坏死和凋亡所致损伤共享p38MAPK激活作为共同的信号转导通路,并且对该激酶进行药理学靶向作用为在缺血/再灌注损伤期间调控这两个过程提供了一个可行的选择。