Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A

被引:473
作者
Oliver, PM
Fox, JE
Kim, R
Rockman, HA
Kim, HS
Reddick, RL
Pandey, KN
Milgram, SL
Smithies, O
Maeda, N
机构
[1] Univ N Carolina, Dept Pathol, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Med, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Physiol, Chapel Hill, NC 27599 USA
[4] Univ Texas, Hlth Sci Ctr, Dept Pathol, San Antonio, TX 78284 USA
[5] Med Coll Georgia, Dept Biochem & Mol Biol, Augusta, GA 30912 USA
关键词
gene targeting; echocardiography; cardiac dilatation; interstitial fibrosis; aortic dissection;
D O I
10.1073/pnas.94.26.14730
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Natriuretic peptides, produced in the heart, bind to the natriuretic peptide receptor A (NPRA) and cause vasodilation and natriuresis important in the regulation of blood pressure, We here report that mice lacking a functional Npr1 gene coding for NPRA have elevated blood pressures and hearts exhibiting marked hypertrophy with interstitial fibrosis resembling that seen in human hypertensive heart disease, Echocardiographic evaluation of the mice demonstrated a compensated state of systemic hypertension in which cardiac hypertrophy and dilatation are evident but with no reduction in ventricular performance, Nevertheless, sudden death, with morphologic evidence indicative in some animals of congestive heart failure and in others of aortic dissection, occurred in all 15 male mice lacking Npr1 before 6 months of age, and in one of 16 females in our study, Thus complete absence of NPRA causes hypertension in mice and leads to cardiac hypertrophy and, particularly in males, lethal vascular events similar to those seen in untreated human hypertensive patients.
引用
收藏
页码:14730 / 14735
页数:6
相关论文
共 27 条
  • [1] PURIFICATION, SEQUENCING AND SYNTHESIS OF NATRIURETIC AND VASOACTIVE RAT ATRIAL PEPTIDE
    ATLAS, SA
    KLEINERT, HD
    CAMARGO, MJ
    JANUSZEWICZ, A
    SEALEY, JE
    LARAGH, JH
    SCHILLING, JW
    LEWICKI, JA
    JOHNSON, LK
    MAACK, T
    [J]. NATURE, 1984, 309 (5970) : 717 - 719
  • [2] DEVEREUX RB, 1990, HYPERTENSION PATHOPH, P359
  • [3] NATRIURETIC HORMONES
    ESPINER, EA
    RICHARDS, AM
    YANDLE, TG
    NICHOLLS, MG
    [J]. ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 1995, 24 (03) : 481 - &
  • [4] DYSREGULATION OF ATRIAL-NATRIURETIC-FACTOR IN HYPERTENSION-PRONE MAN
    FERRARI, P
    WEIDMANN, P
    FERRIER, C
    DIETLER, R
    HOLLMANN, R
    PISO, RJ
    WEY, J
    SHAW, S
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1990, 71 (04) : 944 - 951
  • [5] GARBERS DL, 1994, J BIOL CHEM, V269, P30741
  • [6] PREMATURE MORTALITY FROM CORONARY HEART DISEASE - FRAMINGHAM STUDY
    GORDON, T
    KANNEL, WB
    [J]. JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1971, 215 (10): : 1617 - &
  • [7] HUANG PL, 1995, NATURE, V377, P196
  • [8] IMPAIRED RELEASE OF ATRIAL NATRIURETIC FACTOR IN NACL-LOADED SPONTANEOUSLY HYPERTENSIVE RATS
    JIN, HK
    CHEN, YF
    YANG, RH
    MENG, QC
    OPARIL, S
    [J]. HYPERTENSION, 1988, 11 (06) : 739 - 744
  • [9] GENETIC DECREASES IN ATRIAL-NATRIURETIC-PEPTIDE AND SALT-SENSITIVE HYPERTENSION
    JOHN, SWM
    KREGE, JH
    OLIVER, PM
    HAGAMAN, JR
    HODGIN, JB
    PANG, SC
    FLYNN, TG
    SMITHIES, O
    [J]. SCIENCE, 1995, 267 (5198) : 679 - 681
  • [10] GENETIC-CONTROL OF BLOOD-PRESSURE AND THE ANGIOTENSINOGEN LOCUS
    KIM, HS
    KREGE, JH
    KLUCKMAN, KD
    HAGAMAN, JR
    HODGIN, JB
    BEST, CF
    JENNETTE, JC
    COFFMAN, TM
    MAEDA, N
    SMITHIES, O
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (07) : 2735 - 2739