Cellular protection by erythropoietin: new therapeutic implications?
نویسنده
چکیده
Erythropoietin (EPO), the principal hematopoietic hormone produced by the kidney and the liver in fetuses, regulates mammalian erythropoiesis and exhibits diverse cellular effects in nonhematopoietic tissues. The introduction of recombinant human EPO (rhEPO) has marked a significant advance in the management of anemia associated with chronic renal failure. At the same time, experimental studies have unveiled its potential neuroprotective and cardioprotective properties, occurring independently of its hematopoietic action. As with other cytoprotective agents, administration of exogenous rhEPO can confer cerebral and myocardial protection against ischemia-reperfusion injury in terms of reduction in cellular apoptosis and necrosis, as well as improvement in functional recovery. Very recent studies even suggest that this drug could have beneficial applications in oncology, protecting against chemotherapy cardiotoxicity. The purpose of this letter is to review current information regarding the various conditions in which rhEPO and its derivates could confer cellular protection. We also address clinical perspectives and novel therapeutic strategies that could be developed based on these studies. Thus, EPO seems to be a very promising agent for protecting cellular survival during both acute and chronic diseases, and its future should be considered with enthusiasm.
منابع مشابه
Erythropoietin on a tightrope: balancing neuronal and vascular protection between intrinsic and extrinsic pathways.
Enthusiasm for erythropoietin (EPO) as a broad cytoprotective agent continues to increase at an almost exponential rate. The premise that EPO was required only for erythropoiesis was eventually shed by recent work demonstrating the existence of EPO and its receptor in other organs and tissues outside of the liver and the kidney, such as the brain and heart. As a result, EPO has been identified ...
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BACKGROUND Preconditioning phenomena provide evidence for adaptive responses to ischemia that have important implications for treatment/prevention of myocardial infarction. Hypoxia-inducible factor 1 (HIF-1) mediates adaptive transcriptional responses to hypoxia/ischemia. METHODS AND RESULTS Exposure of wild-type mice to intermittent hypoxia resulted in protection of isolated hearts against i...
متن کاملDoes erythropoietin slow progression of chronic kidney disease?
*Corresponding author: Ali Ghorbani, Department of Nephrology, Golestan Hospital, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran. E-mail: [email protected] Implication for health policy/practice/research/medical education: The initiation of erythropoietin therapy for the purpose of renoprotection may need to be sooner than that for erythropoiesis, because erythropoietin may...
متن کاملبررسی رابطه درمان ترومبولیتیک در سطح اریتروپویتین پلاسما در انفارکتوس حاد میوکارد
Background and purpose: Myocardial Infraction (MI) is one of the most common diseases in industrial countries. In clinical findings, erythropoietin has shown protection against cellular hypoxic ischemic injury in myocardium. This study assessed the role of erythropoietin in patients with acute MI. Materials and methods: In this cohort study 70 patients with STEMI were divided to two groups: (S...
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Recent studies have suggested that the brain preconditioning could induce tolerance to ischemia in humans. It has been believed that newly synthesized proteins are required for the acquisition of delayed tolerance in the brain and spinal cord. However, the mechanism other than the synthesis of neuroprotective proteins may also play a pivotal role. Preconditioning may reprogram the response to i...
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عنوان ژورنال:
- The Journal of pharmacology and experimental therapeutics
دوره 323 3 شماره
صفحات -
تاریخ انتشار 2007