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p38丝裂原活化蛋白激酶抑制剂SB203580可消除大鼠心脏的缺血预处理,但给药时间至关重要。

The p38 MAPK inhibitor, SB203580, abrogates ischaemic preconditioning in rat heart but timing of administration is critical.

作者信息

Mocanu M M, Baxter G F, Yue Y, Critz S D, Yellon D M

机构信息

The Hatter Institute for Cardiovascular Studies, Division of Cardiology, University College London Hospitals & Medical School, UK.

出版信息

Basic Res Cardiol. 2000 Dec;95(6):472-8. doi: 10.1007/s003950070023.

Abstract

There is debate concerning the involvement of p38 mitogen activated protein kinase (MAPK) in the mediation of ischaemic preconditioning. Pharmacological inhibition of p38 MAPK with SB203580 has been reported to block preconditioning in some studies but not in others. We hypothesised that this divergence could be due to differences in the timing of inhibitor administration. Isolated rat hearts were perfused in the Langendorff mode and subjected to 35 min regional ischaemia followed by 120 min reperfusion. Hearts were then double stained with Evans' blue and triphenyltetrazolium chloride to determine risk (R) and infarct zones (I), expressed as I/R% ratios. Preconditioned hearts were subjected to 2 times 5 min global ischaemia with 10 min intervening reperfusion. SB203580 10 microM was perfused either during the preconditioning protocol (PC+/-SB-early),just prior to and during the first 15 min of the lethal ischaemia (PC+/-SB-late) or prior to regional ischaemia in the absence of preconditioning. Ischaemic preconditioning significantly limited infarct size (I/R 38.9 +/- 3.0% in control vs 13.4 +/- 2.4%, P < 0.01). In the PC+/-SB-early group, preconditioning was still fully protective (I/R% 14.6 +/- 1.0). However, in the PC+/-SB-late group, SB203580 completely blocked the protection afforded by preconditioning (I/R% 33.6 +/- 4.4%, P < 0.01 vs 13.4 +/- 2.4% in preconditioned hearts, p < 0.05). SB203580 alone did not affect infarct size when given prior to and during regional ischaemia (I/R 36.2 +/- 2.7%). These histological data are corroborated by a significant increase in p38 MAPK activation in the preconditioned hearts during sustained ischaemia in comparison with the controls. In conclusion the activation of p38 MAPK during lethal ischaemia, but not during the ischaemic preconditioning protocol, is essential for the mediation of protection and may resolve some of the earlier controversy surrounding the use of SB203580 in preconditioning studies.

摘要

关于p38丝裂原活化蛋白激酶(MAPK)是否参与缺血预处理的介导存在争议。在一些研究中,据报道用SB203580对p38 MAPK进行药理学抑制可阻断预处理,但在其他研究中则不然。我们推测这种差异可能是由于抑制剂给药时间的不同。将离体大鼠心脏以Langendorff模式灌注,进行35分钟的局部缺血,随后再灌注120分钟。然后用伊文思蓝和氯化三苯基四氮唑对心脏进行双重染色,以确定危险(R)区和梗死区(I),以I/R%比值表示。预处理的心脏进行2次5分钟的全心缺血,中间间隔10分钟再灌注。10微摩尔的SB203580在预处理期间(PC+/-SB-早期)、在致死性缺血的前15分钟及期间(PC+/-SB-晚期)或在没有预处理的情况下在局部缺血之前灌注。缺血预处理显著限制了梗死面积(对照组I/R为38.9 +/- 3.0%,而预处理组为13.4 +/- 2.4%,P < 0.01)。在PC+/-SB-早期组中,预处理仍然具有完全的保护作用(I/R%为14.6 +/- 1.0)。然而,在PC+/-SB-晚期组中,SB203580完全阻断了预处理所提供的保护作用(I/R%为33.6 +/- 4.4%,与预处理心脏中的13.4 +/- 2.4%相比,P < 0.01,P < 0.05)。当在局部缺血期间及之前给予SB203580时,其单独使用并不影响梗死面积(I/R为36.2 +/- 2.7%)。与对照组相比,在持续缺血期间预处理心脏中p38 MAPK的激活显著增加,这些组织学数据得到了证实。总之 在致死性缺血期间而非缺血预处理期间p38 MAPK的激活对于介导保护作用至关重要,这可能解决了一些早期围绕在预处理研究中使用SB203580的争议。

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