Erythropoietin mimics ischemic preconditioning

被引:50
作者
Baker, JE [1 ]
机构
[1] Med Coll Wisconsin, Milwaukee, WI 53226 USA
关键词
heart; myocardial ischemia; myocardial infarction; erythopoietin; protein kinases; potassium channels; nitric oxide; nitric oxide synthase cardioprotection; dosing considerations; timing considerations;
D O I
10.1016/j.vph.2005.02.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Ischemic preconditioning is a powerful endogenous phenomenon in which brief periods of a sub-toxic ischemic insult induce robust protection against future, lengthy, lethal ischemia. The cardioprotective effects of ischemic preconditioning are manifest in all species studieo. so far, including humans. The ability to reproduce the cardioprotective effects of ischemic preconditioning with pharmacological agents raised. the possibility that a drug may ultimately be introduced into clinical practice to treat human hearts undergoing ischemia/reperfusion. Thin chapter focuses on erythropoietin (Epo), a drug that has already been approved for humans and is in current use for the treatment of anemia associated with chronic renal failure, HIV infection, cancer patients on chemotherapy, and to reduce allogenic blood transfusion in surgery patients. Several recent studies have suggested that this cytokine possesses properties far beyond its capacity to produce red blood cells such. as the ability to protect tissues including brain, kidney and heart against injury caused by ischemia/reperfusion. Cardioprotection conferred by Epo has been shown to be equal in magnitude to that conferred by ischemic preconditioning. However, the underlying mechanisms by which. Epo protects the heart against injury caused by ischemia remain unknown. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:233 / 241
页数:9
相关论文
共 75 条
[1]   The role of MAP kinase in TPA-mediated cell cycle arrest of human breast cancer cells [J].
Alblas, J ;
Slager-Davidov, R ;
Steenbergh, PH ;
Sussenbach, JS ;
van der Burg, B .
ONCOGENE, 1998, 16 (01) :131-139
[2]   Low doses of EPO activate MAP kinases but not JAK2-STAT5 in rat vascular smooth muscle cells [J].
Ammarguellat, F ;
Llovera, M ;
Kelly, PA ;
Goffin, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 284 (04) :1031-1038
[3]   Low-dose therapy with the long-acting erythropoietin analogue darbepoetin alpha persistently activates endothelial Akt and attenuates progressive organ failure [J].
Bahlmann, FH ;
Song, R ;
Boehm, SM ;
Mengel, M ;
von Wasielewski, R ;
Lindschau, C ;
Kirsch, T ;
de Groot, K ;
Laudeley, R ;
Niemczyk, E ;
Güler, F ;
Menne, J ;
Haller, H ;
Fliser, D .
CIRCULATION, 2004, 110 (08) :1006-1012
[4]   Erythropoietin regulates endothelial progenitor cells [J].
Bahlmann, FH ;
de Groot, K ;
Spandau, JM ;
Landry, AL ;
Hertel, B ;
Duckett, T ;
Boehm, SM ;
Menne, J ;
Haller, H ;
Fliser, D .
BLOOD, 2004, 103 (03) :921-926
[5]  
Baker JE, 1997, CIRCULATION, V95, P1278
[6]   The effects of normal as compared with low hematocrit values in patients with cardiac disease who are receiving hemodialysis and epoetin [J].
Besarab, A ;
Bolton, WK ;
Browne, JK ;
Egrie, JC ;
Nissenson, AR ;
Okamoto, DM ;
Schwab, SJ ;
Goodkin, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 1998, 339 (09) :584-590
[7]   Prostaglandin-E2 enhances EPO-mediated STAT5 transcriptional activity by serine phosphorylation of CREB [J].
Boer, AK ;
Drayer, AL ;
Rui, H ;
Vellenga, E .
BLOOD, 2002, 100 (02) :467-473
[8]   Interplay between the cardiac renin angiotensin system and JAK-STAT signaling: Role in cardiac hypertrophy, ischemia/reperfusion dysfunction, and heart failure [J].
Booz, GW ;
Day, JNE ;
Baker, KM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2002, 34 (11) :1443-1453
[9]   Cytokine G-protein signaling crosstalk in cardiomyocytes: Attenuation of Jak-STAT activation by endothelin-1 [J].
Booz, GW ;
Day, JNE ;
Speth, R ;
Baker, KM .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2002, 240 (1-2) :39-46
[10]   PHARMACOKINETICS OF RECOMBINANT-HUMAN-ERYTHROPOIETIN APPLIED SUBCUTANEOUSLY TO CHILDREN WITH CHRONIC-RENAL-FAILURE [J].
BRAUN, A ;
DING, R ;
SEIDEL, C ;
FIES, T ;
KURTZ, A ;
SCHARER, K .
PEDIATRIC NEPHROLOGY, 1993, 7 (01) :61-64