MOLECULAR-CLONING OF HAMSTER BRAIN AND ATRIAL-NATRIURETIC-PEPTIDE CDNAS - CARDIOMYOPATHIC HAMSTERS ARE USEFUL MODELS FOR BRAIN AND ATRIAL NATRIURETIC PEPTIDES

被引:26
作者
TAMURA, N
OGAWA, Y
ITOH, H
ARAI, H
SUGA, S
NAKAGAWA, O
KOMATSU, Y
KISHIMOTO, I
TAKAYA, K
YOSHIMASA, T
SHIONO, S
NAKAO, K
机构
[1] KYOTO UNIV,FAC MED,DEPT MED,DIV 2,SAKYO KU,KYOTO 606,JAPAN
[2] SHIONOGI & CO LTD,SHIONOGI RES LABS,OSAKA 553,JAPAN
关键词
CARDIAC HYPERTROPHY; CONGESTIVE HEART FAILURE; GENE EXPRESSION; RADIOIMMUNOASSAY; TISSUE DISTRIBUTION;
D O I
10.1172/JCI117420
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Brain and atrial natriuretic peptides (BNP and ANP) are cardiac hormones with diuretic, natriuretic, and vasodilatory activities. Cardiomyopathic hamsters are widely used animal models of heart failure. Due to the structural divergence of BNP among species, examination on pathophysiological roles of BNP using cardiomyopathic hamsters is so far impossible. We therefore isolated hamster BNP and ANP cDNAs, and investigated synthesis and secretion of these peptides in normal and cardiomyopathic hamsters. The COOH-terminal 32-residue peptide of cloned hamster pre-proBNP with 122 amino acids, preceded by a single arginine residue, supposedly represents hamster BNP showing < 50% homology to rat BNP. Alpha-hamster ANP, 28-residue peptide, is identical to alpha-rat ANP. In hamsters, BNP and ANP occur mainly in the ventricle and the atrium, respectively. The 32-wk-old hypertrophic cardiomyopathic BIO14.6 strain exhibited ventricular hypertrophy. The 32-wk-old dilated cardiomyopathic BIO53.58 strain remained at the stage without apparent heart failure. In BIO14.6 and BIO53.58 strains at this age, ventricular BNP and ANP gene expressions are augmented, and the plasma BNP concentration is elevated to 136 and 108 fmol/ml, respectively, three times greater than the elevated plasma ANP concentration, which well mimics changes of the plasma BNP and ANP concentrations in human heart failure. Cardiomyopathic hamsters, therefore, are useful models to investigate the implication of BNP in human cardiovascular diseases.
引用
收藏
页码:1059 / 1068
页数:10
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