Novel, selective EPO receptor ligands lacking erythropoietic activity reduce infarct size in acute myocardial infarction in rats

[Display omitted] Erythropoietin (EPO) has been shown to protect the heart against acute myocardial infarction in pre-clinical studies, however, EPO failed to reduce infarct size in clinical trials and showed significant safety problems. Here, we investigated cardioprotective effects of two selectiv...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Pharmacological research 2016-11, Vol.113 (Pt A), p.62-70
Hauptverfasser: Kiss, Krisztina, Csonka, Csaba, Pálóczi, János, Pipis, Judit, Görbe, Anikó, Kocsis, Gabriella F., Murlasits, Zsolt, Sárközy, Márta, Szűcs, Gergő, Holmes, Christopher P., Pan, Yijun, Bhandari, Ashok, Csont, Tamás, Shamloo, Mehrdad, Woodburn, Kathryn W., Ferdinandy, Péter, Bencsik, Péter
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:[Display omitted] Erythropoietin (EPO) has been shown to protect the heart against acute myocardial infarction in pre-clinical studies, however, EPO failed to reduce infarct size in clinical trials and showed significant safety problems. Here, we investigated cardioprotective effects of two selective non-erythropoietic EPO receptor ligand dimeric peptides (AF41676 and AF43136) lacking erythropoietic activity, EPO, and the prolonged half-life EPO analogue, darbepoetin in acute myocardial infarction (AMI) in rats. In a pilot study, EPO at 100U/mL significantly decreased cell death compared to vehicle (33.8±2.3% vs. 40.3±1.5%, p
ISSN:1043-6618
1096-1186
DOI:10.1016/j.phrs.2016.08.013