| Literature DB >> 12914775 |
Gábor Földes1, Ferenc Horkay, István Szokodi, Olli Vuolteenaho, Mika Ilves, Ken A Lindstedt, Mikko Mäyränpää, Balázs Sármán, Leila Seres, Réka Skoumal, Zoltán Lakó-Futó, Rudolf deChâtel, Heikki Ruskoaho, Miklós Tóth.
Abstract
The orphan receptor APJ and its recently identified endogenous ligand, apelin, are expressed in the heart. However, their importance in the human cardiovascular system is not known. This study shows that apelin-like immunoreactivity is abundantly present in healthy human heart and plasma. Gel filtration HPLC analysis revealed that atrial and plasma levels of high molecular weight apelin, possibly proapelin, were markedly higher than those of mature apelin-36 itself. As assessed by quantitative RT-PCR analysis, left ventricular apelin mRNA levels were increased 4.7-fold in chronic heart failure (CHF) due to coronary heart disease (p<0.01) and 3.3-fold due to idiopathic dilated cardiomyopathy (p<0.05), whereas atrial apelin mRNA levels were unchanged. Atrial and plasma apelin-like immunoreactivity as well as atrial and ventricular APJ receptor mRNA levels were significantly decreased in CHF. Our results suggest that a new cardiac regulatory peptide, apelin, and APJ receptor may contribute to the pathophysiology of human CHF.Entities:
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Year: 2003 PMID: 12914775 DOI: 10.1016/s0006-291x(03)01424-4
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575