Volume 103, Issue 2 pp. 124-130

l-Arginine Inhibits Isoproterenol-Induced Cardiac Hypertrophy through Nitric Oxide and Polyamine Pathways

Yan Lin

Yan Lin

Departments of Pathophysiology and

Department of Pathophysiology, Qiqihaer Medical college, Qiqihaer, China, and

Search for more papers by this author
Li-Na Wang

Li-Na Wang

Departments of Pathophysiology and

Search for more papers by this author
Yu-Hui Xi

Yu-Hui Xi

Departments of Pathophysiology and

Search for more papers by this author
Hong-Zhu Li

Hong-Zhu Li

Departments of Pathophysiology and

Search for more papers by this author
Feng-Gang Xiao

Feng-Gang Xiao

Department of Pathophysiology, Qiqihaer Medical college, Qiqihaer, China, and

Search for more papers by this author
Ya-Jun Zhao

Ya-Jun Zhao

Departments of Pathophysiology and

Search for more papers by this author
Ye Tian

Ye Tian

Departments of Pathophysiology and

Search for more papers by this author
Bao-Feng Yang

Bao-Feng Yang

Pharmacology, Harbin Medical University, Harbin, China,

Biopharmaceutical Key Laboratory of Heilongjiang Province, Harbin, China

Search for more papers by this author
Chang-Qing Xu

Chang-Qing Xu

Departments of Pathophysiology and

Biopharmaceutical Key Laboratory of Heilongjiang Province, Harbin, China

Search for more papers by this author
First published: 19 July 2008
Citations: 34
Author for correspondence: Chang-Qing Xu, Department of Pathophysiology, Harbin Medical University, Harbin150086, China (fax +86 451 87503325, e-mail [email protected]).

Abstract

Abstract: Polyamines (putrescine, spermidine and spermine) are essential for cell growth and differentiation. Nitric oxide exhibits antihypertrophic functions and inhibits cardiac remodelling. However, the metabolism of polyamines and the potential interactions with nitric oxide in cardiac hypertrophy remain unclear. We randomly divided Wistar rats into four treatment groups: controls, isoproterenol (ISO), ISO and l-arginine, and l-arginine. Isoproterenol (5 mg/kg/day, subcutaneously) and/or l-arginine (800 mg/kg/day, intraperitoneally) was administered once daily for 7 days. The expression of atrial natriuretic peptide mRNA was determined by reverse transcription–polymerase chain reaction, and fibrogenesis of heart was assessed by Van Gieson staining. Polyamines were measured with high-performance liquid chromatography, and plasma nitric oxide content and lactate dehydrogenase (LDH) activity were determined with a spectrophotometer. The expression levels of ornithine decarboxylase, spermidine/spermine N1-acetyltransferase (SSAT), endothelial nitric oxide synthase (eNOS) and inducible nitric oxide synthase (iNOS) were analysed by Western blot. Heart-to-body weight ratio, left ventricle-to-body weight ratio, atrial natriuretic peptide mRNA expression, collagen fibres and LDH activity were elevated, both ornithine decarboxylase and SSAT proteins were up-regulated, and total polyamines were increased in the group treated with ISO. Additionally, the expression of iNOS was up-regulated, eNOS was down-regulated, and nitric oxide levels were low. Notably, cotreatment with l-arginine reversed most of these changes except for SSAT expression, which was further up-regulated. We propose that increased polyamines and decreased nitric oxide are involved in cardiac hypertrophy induced by ISO and suggest that l-arginine pre-treatment can attenuate cardiac hypertrophy through the regulation of key enzymes of the polyamine and nitric oxide pathways.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.