Literature DB >> 9575953

Prevention of reflex natriuresis after acute unilateral nephrectomy by melanocortin receptor antagonists.

X P Ni1, R A Kesterson, S D Sharma, V J Hruby, R D Cone, E Wiedemann, M H Humphreys.   

Abstract

gamma-Melanocyte-stimulating hormone (gamma-MSH), atrial natriuretic peptide (ANP), and oxytocin have been identified as candidate hormonal mediators of the reflex natriuresis that follows acute unilateral nephrectomy (AUN). Pharmacological characterization of the third melanocortin receptor (MC3-R) indicates that it uniquely responds to physiological concentrations of gamma-MSH. We tested the roles of gamma-MSH, ANP, and oxytocin in the postnephrectomy natriuresis by carrying out AUN during continuous intrarenal infusion of specific antagonists for their cognate receptors. In anesthetized Sprague-Dawley rats, urinary sodium excretion (UNaV) increased from 0.34 +/- 0.04 to 1.12 +/- 0.11 mu eq/min 90 min after AUN (P < 0.001). No change in UNaV occurred in rats undergoing a sham AUN procedure. Plasma immunoreactive gamma-MSH concentration was 53 +/- 8 fmol/ml after sham AUN but 112 +/- 17 fmol/ml after AUN (P < 0.01). SHU-9119 and SHU-9005 are substituted derivatives of alpha-MSH with potent antagonism at the MC3-R in vitro. Infusion of these compounds at 5 pmol/min completely blocked the natriuretic response to AUN despite a similar elevation in plasma gamma-MSH (111 +/- 12 vs. 49 +/- 8 fmol/ml in sham rats, P < 0.01). Intrarenal infusion of the ANP receptor antagonist A-71915 (5 pmol/min) or the oxytocin receptor antagonist [d(CH2)(5)1, Tyr(Me)2,Orn8] vasotocin (10 pmol/min) effectively inhibited the natriuresis induced by intravenous infusion of ANP or oxytocin (each at 1 pmol/min), respectively, but did not block the natriuresis after AUN. Plasma immunoreactivity of these peptides was not increased after AUN. These results indicate that reflex natriuresis after AUN is accompanied by an increase in plasma gamma-MSH but not ANP or oxytocin concentration and is prevented by intrarenal infusion of receptor antagonists with selectivity for MC3-R. The data indicate that gamma-MSH or a closely related peptide mediates postnephrectomy natriuresis and provide further support for the possibility that gamma-MSH may play a wider role in sodium homeostasis.

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Year:  1998        PMID: 9575953     DOI: 10.1152/ajpregu.1998.274.4.R931

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  10 in total

Review 1.  The role of the central melanocortin system in the regulation of food intake and energy homeostasis: lessons from mouse models.

Authors:  Kate L J Ellacott; Roger D Cone
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2006-07-29       Impact factor: 6.237

Review 2.  Melanotropins as drugs for the treatment of obesity and other feeding disorders: potential and problems.

Authors:  Minying Cai; Joel Nyberg; Victor J Hruby
Journal:  Curr Top Med Chem       Date:  2009       Impact factor: 3.295

Review 3.  Cardiovascular effects of melanocortins.

Authors:  Michael H Humphreys; Xi-Ping Ni; David Pearce
Journal:  Eur J Pharmacol       Date:  2011-01-01       Impact factor: 4.432

Review 4.  Physiological roles of the melanocortin MC₃ receptor.

Authors:  Benjamin J Renquist; Rachel N Lippert; Julien A Sebag; Kate L J Ellacott; Roger D Cone
Journal:  Eur J Pharmacol       Date:  2011-01-03       Impact factor: 4.432

5.  The natriuretic mechanism of Gamma-Melanocyte-Stimulating Hormone.

Authors:  Paru P Kathpalia; Carol Charlton; Madhumitha Rajagopal; Alan C Pao
Journal:  Peptides       Date:  2011-02-16       Impact factor: 3.750

Review 6.  Organic chemistry and biology: chemical biology through the eyes of collaboration.

Authors:  Victor J Hruby
Journal:  J Org Chem       Date:  2009-12-18       Impact factor: 4.354

7.  Evidence for a noradrenergic mechanism causing hypertension and abnormal glucose metabolism in rats with relative deficiency of gamma-melanocyte-stimulating hormone.

Authors:  Xi-Ping Ni; Claudia van Dijk; David Pearce; Michael H Humphreys
Journal:  Exp Physiol       Date:  2009-05-08       Impact factor: 2.969

8.  Genetic disruption of gamma-melanocyte-stimulating hormone signaling leads to salt-sensitive hypertension in the mouse.

Authors:  Xi-Ping Ni; David Pearce; Andrew A Butler; Roger D Cone; Michael H Humphreys
Journal:  J Clin Invest       Date:  2003-04       Impact factor: 14.808

9.  Dietary sodium modulates mRNA abundance of enzymes involved in pituitary processing of proopiomelanocortin.

Authors:  G Chandramohan; X P Ni; J E Kalinyak; M H Humphreys
Journal:  Pituitary       Date:  2001-09       Impact factor: 4.107

10.  α-MSH analogue attenuates blood pressure elevation in DOCA-salt hypertensive mice.

Authors:  Petteri Rinne; Anna-Maija Penttinen; Wendy Nordlund; Markku Ahotupa; Eriika Savontaus
Journal:  PLoS One       Date:  2013-08-16       Impact factor: 3.240

  10 in total

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