Literature DB >> 15911062

Biology of natriuretic peptides and their receptors.

Kailash N Pandey1.   

Abstract

Increasing evidence suggests that natriuretic peptides (NPs) play diverse roles in mammals, including renal hemodynamics, neuroendocrine, and cardiovascular functions. Collectively, NPs are classified as hypotensive hormones; the main actions of NPs are implicated in eliciting natriuretic, diuretic, steroidogenic, antiproliferative, and vasorelaxant effects, important factors in the control of body fluid volume and blood pressure homeostasis. One of the principal loci involved in the regulatory actions of NPs is their cognate plasma membrane receptor molecules, which are activated by binding with specific NPs. Interaction of NPs with their receptors plays a central role in physiology and pathophysiology of hypertension and cardiovascular disorders. Gaining insight into the intricacies of NPs-specific receptor signaling pathways is of pivotal importance for understanding both hormone-receptor biology and the disease states arising from abnormal hormone receptor interplay. During the last decade there has been a surge in interest in NP receptors; consequently, a wealth of information has emerged concerning molecular structure and function, signaling mechanisms, and use of transgenics and gene-targeted mouse models. The objective of this present review is to summarize and document the previous findings and recent discoveries in the field of the natriuretic peptide hormone family and receptor systems with emphasis on the structure-function relationship, signaling mechanisms, and the physiological and pathophysiological significance in health and disease.

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Year:  2005        PMID: 15911062     DOI: 10.1016/j.peptides.2004.09.024

Source DB:  PubMed          Journal:  Peptides        ISSN: 0196-9781            Impact factor:   3.750


  71 in total

1.  Genetic disruption of guanylyl cyclase/natriuretic peptide receptor-A upregulates renal (pro) renin receptor expression in Npr1 null mutant mice.

Authors:  Ramu Periyasamy; Subhankar Das; Kailash N Pandey
Journal:  Peptides       Date:  2019-04-06       Impact factor: 3.750

2.  C-type natriuretic peptide stimulates ovarian follicle development.

Authors:  Yorino Sato; Yuan Cheng; Kazuhiro Kawamura; Seido Takae; Aaron J W Hsueh
Journal:  Mol Endocrinol       Date:  2012-05-17

3.  Atrial natriuretic factor receptor guanylate cyclase signaling: new ATP-regulated transduction motif.

Authors:  Teresa Duda; Shashank Bharill; Ireneusz Wojtas; Prem Yadav; Ignacy Gryczynski; Zygmunt Gryczynski; Rameshwar K Sharma
Journal:  Mol Cell Biochem       Date:  2009-01-10       Impact factor: 3.396

4.  Guanylyl cyclase/natriuretic peptide receptor-A signaling antagonizes the vascular endothelial growth factor-stimulated MAPKs and downstream effectors AP-1 and CREB in mouse mesangial cells.

Authors:  Satyabha Tripathi; Kailash N Pandey
Journal:  Mol Cell Biochem       Date:  2012-05-19       Impact factor: 3.396

Review 5.  Proximal nephron.

Authors:  Jia L Zhuo; Xiao C Li
Journal:  Compr Physiol       Date:  2013-07       Impact factor: 9.090

Review 6.  Guanylyl cyclase / atrial natriuretic peptide receptor-A: role in the pathophysiology of cardiovascular regulation.

Authors:  Kailash N Pandey
Journal:  Can J Physiol Pharmacol       Date:  2011-08-04       Impact factor: 2.273

Review 7.  Dual-acting angiotensin receptor-neprilysin inhibition.

Authors:  Julian Segura; Luis M Ruilope
Journal:  Curr Hypertens Rep       Date:  2011-02       Impact factor: 5.369

8.  ANP-mediated inhibition of distal nephron fractional sodium reabsorption in wild-type and mice overexpressing natriuretic peptide receptor.

Authors:  Di Zhao; Kailash N Pandey; L Gabriel Navar
Journal:  Am J Physiol Renal Physiol       Date:  2009-11-11

9.  Clathrin-dependent internalization, signaling, and metabolic processing of guanylyl cyclase/natriuretic peptide receptor-A.

Authors:  Naveen K Somanna; Indra Mani; Satyabha Tripathi; Kailash N Pandey
Journal:  Mol Cell Biochem       Date:  2017-09-12       Impact factor: 3.396

10.  Retinoic acid and sodium butyrate suppress the cardiac expression of hypertrophic markers and proinflammatory mediators in Npr1 gene-disrupted haplotype mice.

Authors:  Umadevi Subramanian; Prerna Kumar; Indra Mani; David Chen; Isaac Kessler; Ramu Periyasamy; Giri Raghavaraju; Kailash N Pandey
Journal:  Physiol Genomics       Date:  2016-05-06       Impact factor: 3.107

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