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Differential regulation of membrane bound guanylyl cyclases (GC) | 48808

Journal of Neuroscience and Neuropharmacology

Differential regulation of membrane bound guanylyl cyclases (GC) during β-adrenergic receptor activation- induced hypertrophic growth in rats

4th Global Experts Meeting on Neuropharmacology

September 14-16, 2016 San Antonio, USA

Elangovan Vellaichamy

University of Madras, India

Scientific Tracks Abstracts: Neurochem Neuropharm

Abstract :

The natriuretic peptides (NPs) family is consists of three important peptides namely atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and C-type natriuretic peptide (CNP). ANP and BNP elicit its physiological action by specific binding to Natriureitc Peptide Receptor-A/Guanylyl cyclase-A (NPR-A/GC-A), while CNP binds to Natriureitc Peptide Receptor-B/ Guanylyl cyclase-B (NPR-B/GC-B). Recent studies have suggested that ANP/NPR-A/GC-A and CNP/ NPR-B/GC-B system are present in the heart as a negative regulatory mechanisms to antagonize the cardiac growth response to hypertrophic stimuli. Since NPs has the potential to inhibit cardiac hypertrophic growth via NPR-A/NPR-B receptors, understanding the regulation and expression of NPR-A and â��B in the heart during the diseased conditions will help to target specific NPRs subtype to increase the physiological actions of NPs, and thus may be useful as therapy for cardiac hypertrophy and heart failure. In this context, we have studied left ventricular (LV) expression of NPR-A and NPR-B, and the functional activity of these receptors during �²-adrenergic receptor (�²-AR) activation induced hypertrophic growth in experimental rats. The NPR-A expression was markedly reduced (3.5-fold), while the NPR-B expression was up regulated (4-fold) in Isoproterenol (ISO)-treated heart as compared with controls. Further, in-vitro membranes assay shows that NPR-A dependent guanylyl cyclase (GC) activity was down-regulated (2-fold), whereas NPR-B dependent GC activity was increased (5-fold) in ISO treated hearts. Beta-blocker (atenolol) treatment normalized the altered expression of NPR-A and â��B proteins. Our results suggest that the chronic �²-AR activation differentially regulates NPR-A/GC-A and NPR-B/GC-B in the heart. The significance of this finding will be discussed during the presentation.

Biography :

Elangovan Vellaichamy has completed his MPhil and PhD (Biochemistry) degree from University of Madras, India and Post-doctoral studies from Hebrew University of Jerusalem, Isreal, The Celveland Clinc Foundation, Cleveland, Ohio and Tualne University of Health Sciences, Louisiana, USA. He is presently working as a Professor for the Department of Biochemistry in University of Madras, Chennai, India. He has published more than 45 papers. His area of research interest is on Natriurteic Peptides and its Receptro System of the heart and understanding the disease mechanisms of hypertension, cardiac hypertrophy and heart failure.

Email: vellaie@gmail.com

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