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Pre-conditioning with adenosine leads to concentration-dependent infarct size reduction in the isolated rabbit heart.

作者信息

Woolfson R G, Patel V C, Yellon D M

机构信息

The Hatter Institute for Cardiovascular Studies, Department of Academic Cardiology, University College London Medical School, UK.

出版信息

Cardiovasc Res. 1996 Jan;31(1):148-51.

PMID:8849599
Abstract

Adenosine (ADO) has a cardioprotective effect in ischemia-reperfusion injury when administered both prior to ischemia and during reperfusion. ADO has also been implicated in the mechanism of ischemic pre-conditioning. The aim of this study was to investigate whether there was a concentration-response between the administration of ADO prior to ischemia-reperfusion and reduction in subsequent infarct size. Rabbit isolated perfused hearts were subjected to 45 min ischemia and 180 min reperfusion following pre-treatment with either Krebs Henseleit buffer alone or buffer containing ADO at a range of concentrations (3 micro M-100 micro M) for 5 min followed by 5 min perfusion with buffer. Infarct/risk ratios were significantly reduced in hearts pre-perfused with higher (> 3 micro M) concentrations of ADO (Control, 58.5 +/- 1.5%; 3 micro M ADO, 51.6 +/- 3.0% ; 6 micro M ADO, 44.1% +/- 2.0%; 10 micro M ADO, 33.3 +/- 1.9%; 20 micro M ADO, 26.6 +/- 0.9%; 50 micro M ADO, 21.6 +/- 3.5%; 100 micro M ADO, 23.0 +/- 0.6%). We conclude that pre-treatment with ADO leads to a concentration-dependent reduction in infarct size.

摘要

相似文献

1
Pre-conditioning with adenosine leads to concentration-dependent infarct size reduction in the isolated rabbit heart.
Cardiovasc Res. 1996 Jan;31(1):148-51.
2
Exogenous adenosine, supplied transiently during reperfusion, ameliorates depressed endogenous adenosine production in the post-ischemic rat heart.在再灌注期间短暂供应的外源性腺苷可改善缺血后大鼠心脏中内源性腺苷生成的抑制。
J Mol Cell Cardiol. 1997 Jan;29(1):333-46. doi: 10.1006/jmcc.1996.0278.
3
Cardioprotective effects of the novel adenosine A1/A2 receptor agonist AMP 579 in a porcine model of myocardial infarction.新型腺苷A1/A2受体激动剂AMP 579在猪心肌梗死模型中的心脏保护作用
J Pharmacol Exp Ther. 1998 Aug;286(2):611-8.
4
Limitation of infarct size in rabbit hearts by the novel adenosine receptor agonist AMP 579 administered at reperfusion.在再灌注时给予新型腺苷受体激动剂AMP 579对兔心脏梗死面积的限制作用
J Mol Cell Cardiol. 2000 Dec;32(12):2339-47. doi: 10.1006/jmcc.2000.1264.
5
Intermittent adenosine at the beginning of reperfusion does not trigger cardioprotection.再灌注开始时给予间歇性腺苷不会引发心脏保护作用。
J Surg Res. 2009 May 15;153(2):231-8. doi: 10.1016/j.jss.2008.02.070. Epub 2008 Apr 8.
6
[Does adenosine administration during the early reperfusion period affect ischemic preconditioning?].[早期再灌注期给予腺苷是否会影响缺血预处理?]
Jpn J Thorac Cardiovasc Surg. 1998 Sep;46(9):860-7. doi: 10.1007/BF03217834.
7
Bradykinin protects against infarction but does not mediate ischemic preconditioning in the isolated rat heart.缓激肽可预防梗死,但在离体大鼠心脏中不介导缺血预处理。
J Mol Cell Cardiol. 1996 Dec;28(12):2333-41. doi: 10.1006/jmcc.1996.0226.
8
Adenosine reduces cardiac TNF-alpha production and human myocardial injury following ischemia-reperfusion.腺苷可减少缺血再灌注后心脏肿瘤坏死因子-α的产生及人类心肌损伤。
J Surg Res. 1998 May;76(2):117-23. doi: 10.1006/jsre.1998.5304.
9
Selective blockade of AT1 angiotensin II receptors abolishes ischemic preconditioning in isolated rabbit hearts.选择性阻断AT1血管紧张素II受体可消除离体兔心脏的缺血预处理。
J Mol Cell Cardiol. 1997 Jan;29(1):129-39. doi: 10.1006/jmcc.1996.0258.
10
Pre-ischemic administration of landiolol prevents ischemia-reperfusion injury in the rat heart.缺血前给予兰地洛尔可预防大鼠心脏的缺血再灌注损伤。
Osaka City Med J. 2007 Jun;53(1):9-16.

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Adenosine receptor subtypes and the heart failure phenotype: translating lessons from mice to man.腺苷受体亚型与心力衰竭表型:将小鼠实验的经验应用于人类
Trans Am Clin Climatol Assoc. 2011;122:198-214.
5
[Ischemic preconditioning in the aged heart--myocardial protective effect as compared with the mature heart].老年心脏的缺血预处理——与成熟心脏相比的心肌保护作用
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6
Loss of glycogen during preconditioning is not a prerequisite for protection of the rabbit heart.预处理期间糖原的丢失并非兔心脏获得保护的必要条件。
Basic Res Cardiol. 1996 Sep-Oct;91(5):374-81. doi: 10.1007/BF00788717.