Angiotensin II dependent cardiac remodeling in the eel Anguilla anguilla involves the NOS/NO system

被引:16
作者
Filice, Mariacristina [1 ]
Aurelio, Daniela [1 ]
Garofalo, Filippo [1 ]
David, Sabrina [2 ]
Fucarino, Alberto [2 ,3 ]
Jensen, Frank Bo [4 ]
Imbrogno, Sandra [1 ]
Cerra, Maria Carmela [1 ]
机构
[1] Univ Calabria, Dept Biol Ecol & Earth Sci BEST, Arcavacata Di Rende, CS, Italy
[2] Univ Palermo, Dept Expt Biomed & Clin Neurosci, Palermo, Italy
[3] Euromediterranean Inst Sci & Technol, Palermo, Italy
[4] Univ Southern Denmark, Dept Biol, Campusvej 55, DK-5230 Odense, Denmark
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2017年 / 65卷
关键词
AT(2) receptor; ERK1-2; Hsp90; Myocardial growth; NOSTRIN; NITRIC-OXIDE SYNTHASE; TYPE-2; RECEPTOR; HEART-FAILURE; FRESH-WATER; HYPOXIC CONDITIONS; ENDOTHELIAL-CELLS; SIGNALING PATHWAY; ENZYME PATTERN; AMERICAN EEL; FISH HEART;
D O I
10.1016/j.niox.2017.02.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Angiotensin II (AngII), the principal effector of the Renin-Angiotensin System (RAS), plays an important role in controlling mammalian cardiac morpho-functional remodelling. In the eel Anguilla anguilla, one month administration of AngII improves cardiac performance and influences the expression and localization of molecules which regulate cell growth. To deeper investigate the morpho-functional chronic influences of AngII on the eel heart and the molecular mechanisms involved, freshwater eels (A. anguilla) were intraperitoneally injected for 2 months with AngII (1 nmol g BW-1). Then the isolated hearts were subjected to morphological and western blotting analyses, and nitrite measurements. If compared to control animals, the ventricle of AngII-treated hearts showed an increase in compacta thickness, vascularization, muscle mass and fibrosis. Structural changes were paralleled by a higher expression of AT(2) receptor and a negative modulation of the ERK1-2 pathway, together with a decrease in nitrite concentration, indicative of a reduced Nitric Oxide Synthase (NOS)-dependent NO production. Moreover, immunolocalization revealed, particularly on the endocardial endothelium (EE) of AngII-treated hearts, a significant reduction of phosphorylated NOS detected by peNOS antibody accompanied by an increased expression of the eNOS disabling protein NOSTRIN, and a decreased expression of the positive regulators of NOS activity, pAkt and Hsp90. On the whole, results suggest that, in the eel, AngII modulates cardiac morpho-functional plasticity by influencing the molecular mechanisms that control NOS activity and the ERK1-2 pathway. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:50 / 59
页数:10
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