DIFFERENTIAL REGULATION OF NATRIURETIC PEPTIDE RECEPTOR MESSENGER-RNAS DURING THE DEVELOPMENT OF CARDIAC-HYPERTROPHY IN THE RAT

被引:75
作者
BROWN, LA [1 ]
NUNEZ, DJR [1 ]
WILKINS, MR [1 ]
机构
[1] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH, DEPT CLIN PHARMACOL, DU CANE RD, LONDON W12 0NN, ENGLAND
关键词
ARTERIOVENOUS SHUNT; ATRIAL NATRIURETIC PEPTIDE; BRAIN NATRIURETIC PEPTIDE; CLEARANCE; GUANYLYL CYCLASE; HEART;
D O I
10.1172/JCI116887
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
The heart expresses the three natriuretic peptide receptors (NPR), namely NPR-A, NPR-B, and NPR-C. We have examined the temporal relationship between the expression of mRNA transcripts for atrial natriuretic peptide (ANP) and brain natriuretic peptide (BNP) and their receptors in the heart during the development of cardiac hypertrophy in the aortovenocaval fistula rat. Messenger RNAs were measured by cDNA amplification. Progressive cardiac hypertrophy was accompanied by increased ANP mRNA prevalence throughout the heart and increased BNP mRNA in the left atrium. The most striking observation was the gradual disappearance of NPR-C transcripts (the putative ''clearance'' receptor) in all chambers; this was in marked contrast to the increase in mRNA levels for NPR-A and NPR-B (the guanylyl cyclase-linked receptors). Our observations have important therapeutic implications if the transcript changes are mirrored at the receptor protein level because (a) the apparent down-regulation of NPR-C may enhance the local action of natriuretic peptides on the heart, and (b) the loss of NPR-C, particularly if it is widespread, may reduce the rate of elimination of the natriuretic peptides, restricting the therapeutic potential of specific NPR-C ligands designed to reduce peptide clearance.
引用
收藏
页码:2702 / 2712
页数:11
相关论文
共 91 条
[1]   DISTRIBUTION AND MOLECULAR-FORMS OF BRAIN NATRIURETIC PEPTIDE IN THE CENTRAL NERVOUS-SYSTEM, HEART AND PERIPHERAL TISSUE OF RAT [J].
ABURAYA, M ;
MINAMINO, N ;
HINO, J ;
KANGAWA, K ;
MATSUO, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 165 (02) :880-887
[2]  
ANANDSRIVASTAVA MB, 1990, J BIOL CHEM, V265, P8566
[3]   ATRIAL-NATRIURETIC-FACTOR RECEPTORS ARE NEGATIVELY COUPLED TO ADENYLATE-CYCLASE IN CULTURED ATRIAL AND VENTRICULAR CARDIOCYTES [J].
ANANDSRIVASTAVA, MB ;
CANTIN, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 138 (01) :427-436
[4]   INHIBITION OF PITUITARY ADENYLATE-CYCLASE BY ATRIAL NATRIURETIC FACTOR [J].
ANANDSRIVASTAVA, MB ;
CANTIN, M ;
GENEST, J .
LIFE SCIENCES, 1985, 36 (19) :1873-1879
[5]  
ANANDSRIVASTAVA MB, 1987, J BIOL CHEM, V262, P4931
[6]   GROWTH-REGULATORY PROPERTIES OF ATRIAL-NATRIURETIC-FACTOR [J].
APPEL, RG .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (06) :F911-F918
[7]   THE PHARMACOKINETICS OF I-125 ATRIAL-NATRIURETIC-FACTOR IN ANESTHETIZED RATS - EFFECTS OF NEUTRAL ENDOPEPTIDASE INHIBITION WITH CANDOXATRILAT AND OF ANF-C RECEPTOR BLOCKADE [J].
BARCLAY, PL ;
BENNETT, JA ;
GREENGRASS, PM ;
GRIFFIN, A ;
SAMUELS, GMR ;
SHEPERSON, NB .
BIOCHEMICAL PHARMACOLOGY, 1992, 44 (06) :1013-1022
[8]   ATRIAL NATRIURETIC FACTOR ALTERS PHOSPHOLIPID-METABOLISM IN MESANGIAL CELLS [J].
BARNETT, R ;
ORTIZ, PA ;
BLAUFOX, S ;
SINGER, S ;
NORD, EP ;
RAMSAMMY, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (01) :C37-C45
[9]  
BENNETT BD, 1991, J BIOL CHEM, V266, P23060
[10]   ANP STIMULATES PHOSPHOLIPASE-C IN CULTURED RIMCT CELLS - ROLES OF PROTEIN-KINASES AND G-PROTEIN [J].
BERL, T ;
MANSOUR, J ;
TEITELBAUM, I .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :F590-F595