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Translational promise of the apelin–APJ system

Heart, 2010
Apelin, the endogenous ligand for the G-protein-coupled APJ receptor, is emerging as a key hormone in cardiovascular homoeostasis. It is expressed in a diverse range of tissues with particular preponderance for the cardiovascular system, being found in both the heart and vasculature. Apelin is the most potent in vitro inotrope yet identified and causes
Gareth, Barnes   +2 more
openaire   +2 more sources

The apelin/APJ signaling system and cytoprotection: Role of its cross-talk with kappa opioid receptor.

European Journal of Pharmacology, 2022
Apelin, a regulatory peptide, is an endogenous ligand of the apelin receptor (APJ), which belongs to the G protein-coupled receptor family. The peptide and its receptor are distributed in animal and human tissues, including the cardiovascular and central
Mehran Ilaghi   +4 more
semanticscholar   +1 more source

First Report on Predictive Comparative Ligand-based Multi-QSAR Modeling Analysis of 4-pyrimidinone and 2-pyridinone based APJ inhibitors

New Journal of Chemistry, 2022
Apelin-apelin receptor (APJ) system has been a promising biomolecular target participating crucially in several major disorders including cardiovascular diseases, neurodegenerative diseases, metabolic disorders, lung, liver, and kidney-related diseases ...
Suvankar Banerjee   +4 more
semanticscholar   +1 more source

Characterization of Apelin, the Ligand for the APJ Receptor

Journal of Neurochemistry, 2000
Abstract: The apelin peptide was recently discovered and demonstrated to be the endogenous ligand for the G protein‐coupled receptor, APJ. A search of the GenBank databases retrieved a rat expressed sequence tag partially encoding the preproapelin sequence.
D K, Lee   +8 more
openaire   +2 more sources

Potential role of the apelin‐APJ pathway in sex‐related differential cardiotoxicity induced by doxorubicin in mice

Journal of Applied Toxicology, 2022
Preclinical and clinical findings suggest sexual dimorphism in cardiotoxicity induced by a chemotherapeutic drug, doxorubicin (DOX). However, molecular alterations leading to sex‐related differential vulnerability of heart to DOX toxicity are not fully ...
V. Desai   +9 more
semanticscholar   +1 more source

Elabela ameliorates neuronal pyroptosis and mitochondrial fission via APJ/ZBP1 signaling in ischemic stroke.

Experimental Neurology
Pyroptosis signifies a significant form of programmed neuronal demise subsequent to ischemic stroke. In our prior investigations, we demonstrated that the Elabela (ELA)-Apelin receptor (APJ) axis alleviated neuronal death by improving collateral ...
Nan Shen   +8 more
semanticscholar   +1 more source

APJ/apelin: a promising target for the treatment of retinopathy of prematurity.

Drug Discovery Today, 2022
Retinopathy of prematurity is a noticeable retinal abnormality causing common blindness in children. An uncontrolled retinal vasculature in retinopathy of prematurity inflicts vision loss in numerous children despite the accessibility to a wide range of ...
Jingtian Su   +5 more
semanticscholar   +1 more source

The Apelin/APJ System

High Blood Pressure & Cardiovascular Prevention, 2006
Apelin, the endogenous ligand of the G protein-coupled APJ receptor, displays several activities on the cardiovascular system. Indeed, recent studies support the notion that the apelin/APJ system is involved in key mechanisms that are relevant to fluid homeostasis, blood pressure control and cardiac contractility.
FRANCIA, Pietro   +3 more
openaire   +2 more sources

Apelin and its receptor APJ in cardiovascular diseases

Clinica Chimica Acta, 2014
Apelin is an adipokine that has been identified as an endogenous ligand for the orphan receptor APJ. Apelin and APJ are expressed in a diverse range of tissues with particular preponderance for the heart and vasculature. Apelin has powerful positive inotropic actions and causes endothelium- and nitric oxide-dependent vasodilatation.
Xiao-Hua, Yu   +7 more
openaire   +2 more sources

The apelin–APJ system in heart failure

Biochemical Pharmacology, 2008
David E Newby, Alan G Japp
exaly   +2 more sources

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