Activation of a GPCR, ORL1 receptor: A novel therapy to prevent heart failure progression
Saliha Pathan, Aarthi Pugazenthi, Beverly REA Dixon, Theodore G Wensel, Todd K Rosengart, Megumi Mathison

TL;DR
Activating the ORL1 receptor with MCOPPB improves heart function and reduces damage after heart attacks in rats, offering a new treatment for heart failure.
Contribution
MCOPPB, an ORL1 activator, is shown to prevent heart failure progression in a rat model through improved cardiac function and reduced fibrosis.
Findings
MCOPPB significantly improved ejection fraction in rats compared to saline.
MCOPPB reduced fibrosis and promoted angiogenesis in heart tissue.
ORL1 activation may serve as a novel therapy to prevent heart failure progression.
Abstract
The number of ischemic heart failure (HF) patients is growing dramatically worldwide. However, there are at present no preventive treatments for HF. Our previous study showed that Gata4 overexpression improved cardiac function after myocardial infarction in the rat heart. We also found that Gata4 overexpression significantly increased a Pnoc gene expression, an endogenous ligand for cell membrane receptor, ORL1. We hypothesized that an activation of ORL1 receptor would suppress HF in a rat ischemic heart model. Adult Sprague Dawley rats (8 weeks old, 6 males and 6 females) underwent left anterior descending coronary artery ligation. Three weeks later, normal saline or MCOPPB (ORL1 activator, 2.5mg/kg/day) intraperitoneal injection was started, and continued 5 days a week, for 3 months. Echocardiography was performed six times, pre-operative, 3 days after coronary artery ligation,…
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Taxonomy
TopicsReceptor Mechanisms and Signaling · Neuropeptides and Animal Physiology · Signaling Pathways in Disease
