Literature DB >> 21722652

The biological effect of pharmacological treatment on dimethylaminohydrolases (DDAH-1) and cationic amino acid transporter-1 (CAT-1) expression in patients with acute congestive heart failure.

Lorenza Speranza1, Sara Franceschelli, Nicolantonio D'Orazio, Raffaella Gaeta, Tonino Bucciarelli, Mario Felaco, Alfredo Grilli, Graziano Riccioni.   

Abstract

AIM: Asymmetric dimethylarginine (ADMA) is an endogenous inhibitor of nitric oxide (NO) which plays an important role in controlling vascular tone and regulates the contractile properties of cardiac myocytes. The aim of this study was to investigate the effect of pharmacological treatment on symmetric dimethylarginine (SDMA), ADMA and arginine plasma concentrations in patients with acute congestive heart failure (ACHF) through the evaluation of type-1 system cationic amino acid transporter-1/type 1 dimethylarginine dimethylaminohydrolases-1 (CAT-1/DDAH-1). METHODS AND
RESULTS: 25 hospitalized cardiology patients with symptomatic acute congestive HF (NYHA Class III-IV) and impaired left ventricular (LV) function (ejection fraction<35%) were included in the study. ADMA, SDMA, and arginine plasma concentrations were assessed before and after pharmacological treatment by high performance liquid chromatography. All patients received an adequate pharmacological treatment for ACHF. ADMA and SDMA plasma levels were significantly higher after pharmacological treatment respect to baseline values (pre-treatment) (0.75 vs 0.48; 1.31 vs 1.03; p<0.01). Arginine plasma concentration was significantly lower after therapy respect to baseline values (0.78 vs 0.99; p<0.01). This is associated more with the modulation of DDAH-1 protein than with of CAT-1 system transport.
CONCLUSIONS: In patients with ACHF, acute renal impairment function and the modulation of metabolism and extracellular transport by the DDAH-1/CAT-1 system determine high ADMA and SDMA levels after therapy for acute congestive heart failure.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21722652     DOI: 10.1016/j.mvr.2011.06.003

Source DB:  PubMed          Journal:  Microvasc Res        ISSN: 0026-2862            Impact factor:   3.514


  3 in total

1.  DDAH-1, via regulation of ADMA levels, protects against ischemia-induced blood-brain barrier leakage.

Authors:  Yichen Zhao; Xiaoye Ma; Yuchen Zhou; Junchao Xie; Xueyuan Liu; Yanxin Zhao
Journal:  Lab Invest       Date:  2021-02-11       Impact factor: 5.662

2.  Biological functional relevance of asymmetric dimethylarginine (ADMA) in cardiovascular disease.

Authors:  Sara Franceschelli; Alessio Ferrone; Mirko Pesce; Graziano Riccioni; Lorenza Speranza
Journal:  Int J Mol Sci       Date:  2013-12-16       Impact factor: 5.923

3.  Prognostic Value of Asymmetric Dimethylarginine in Patients with Heart Failure: A Systematic Review and Meta-analysis.

Authors:  Wenjun Pan; Baotao Lian; Haining Lu; Pengda Liao; Liheng Guo; Minzhou Zhang
Journal:  Biomed Res Int       Date:  2020-07-04       Impact factor: 3.411

  3 in total

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