Atrial natriuretic peptide and oxidative stress

被引:40
作者
De Vito, Paolo [1 ]
Incerpi, Sandra [2 ]
Pedersen, Jens Z. [1 ]
Luly, Paolo [1 ]
机构
[1] Univ Roma Tor Vergata, Dept Biol, Via Ric Sci 1, I-00133 Rome, Italy
[2] Univ Rome Roma Tre, Dept Biol, I-00146 Rome, Italy
关键词
ANP; Reactive oxygen species; Superoxide; Antioxidant; SMOOTH-MUSCLE-CELLS; SPONTANEOUSLY HYPERTENSIVE-RATS; LEFT-VENTRICULAR HYPERTROPHY; NITRIC-OXIDE SYNTHASE; NADPH OXIDASE; REACTIVE OXYGEN; HEART-FAILURE; LYSOPHOSPHATIDIC ACID; PRESSURE-OVERLOAD; GENE-EXPRESSION;
D O I
10.1016/j.peptides.2010.04.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atrial natriuretic peptide (ANP) is a hormone, produced mainly by cardiomyocytes, with a major role in cardiovascular homeostatic mechanisms such as natriuresis and vasodilation, which serve to regulate blood pressure. However, ANP also acts as an autocrine/paracrine factor on other targets such as kidney, lung, thymus, liver and the immune system. ANP participates in the regulation of cell growth and proliferation, and evidence is accumulating that these effects are associated with the generation of reactive oxygen species (ROS). In vascular cells and cardiomyocytes ANP stimulates the antioxidant defense, but in other systems such as hepatoblastoma and macrophages ANP may produce either antioxidant or prooxidant effects, depending on experimental conditions and cell context. At present very little is known on the relationship between ANP and ROS production in the normal homeostatic processes or during the development of cardiovascular diseases and cancer. Our current knowledge of the role of ANP in signaling pathways leading to the generation of intracellular messengers such as diacylglycerol (DAG), and guanosine 3'-5'-cyclic monophosphate has been examined in order to clarify the mechanisms by which the hormone may counteract or contribute to the potentially dangerous effects of free radicals. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:1412 / 1419
页数:8
相关论文
共 105 条
[81]   Role of hydrogen peroxide and oxidative stress in healing responses [J].
Rojkind, M ;
Domínguez-Rosales, JA ;
Nieto, N ;
Greenwel, P .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2002, 59 (11) :1872-1891
[82]   The atrial natriuretic peptide: a changing view [J].
Rubattu, S ;
Volpe, M .
JOURNAL OF HYPERTENSION, 2001, 19 (11) :1923-1931
[83]  
RUSKOAHO H, 1992, PHARMACOL REV, V574, P481
[84]   Activation of natriuretic peptide receptor-C attenuates the enhanced oxidative stress in vascular smooth muscle cells from spontaneously hypertensive rats:: Implication of Giα protein [J].
Saha, Soumya ;
Li, Yuan ;
Lappas, Georgios ;
Anand-Srivastava, Madhu B. .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2008, 44 (02) :336-344
[85]   NOX5, a New "Radical" Player in Human Atherosclerosis? [J].
Schulz, Eberhard ;
Muenzel, Thomas .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2008, 52 (22) :1810-1812
[86]   Molecular mechanisms of hypertension: role of Nox family NADPH oxidases [J].
Sedeek, Mona ;
Hebert, Richard L. ;
Kennedy, Chris R. ;
Burns, Kevin D. ;
Touyz, Rhian M. .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2009, 18 (02) :122-127
[87]   Predominant effect of A-type natriuretic peptide on reduction of oxidative stress during the treatment of patients with heart failure [J].
Shono, Makoto ;
Yoshimura, Michihiro ;
Nakayama, Masafumi ;
Yamamuro, Megumi ;
Abe, Koji ;
Suzuki, Satoru ;
Mizuno, Yuji ;
Sugiyama, Seigo ;
Saito, Yoshihiko ;
Nakao, Kazuwa ;
Yasue, Hirofumi ;
Ogawa, Hisao .
CIRCULATION JOURNAL, 2007, 71 (07) :1040-1046
[88]   Beneficial effects of long-term use of the antioxidant probucol in heart failure in the rat [J].
Sia, YT ;
Lapointe, N ;
Parker, TG ;
Tsoporis, JN ;
Deschepper, CF ;
Calderone, A ;
Pourdjabbar, A ;
Jasmin, JF ;
Sarrazin, JF ;
Liu, P ;
Adam, A ;
Butany, J ;
Rouleau, JL .
CIRCULATION, 2002, 105 (21) :2549-2555
[89]   Natriuretic peptide signalling - Molecular and cellular pathways to growth regulation [J].
Silberbach, M ;
Roberts, CT .
CELLULAR SIGNALLING, 2001, 13 (04) :221-231
[90]   Inhibition of copper-zinc superoxide dismutase induces cell growth, hypertrophic phenotype, and apoptosis in neonatal rat cardiac myocytes in vitro [J].
Siwik, DA ;
Tzortzis, JD ;
Pimental, DR ;
Chang, DLF ;
Pagano, PJ ;
Singh, K ;
Sawyer, DB ;
Colucci, WS .
CIRCULATION RESEARCH, 1999, 85 (02) :147-153