TIME COURSE OF STIMULATION OF RENAL RENIN MESSENGER-RNA BY FUROSEMIDE

被引:24
作者
CHEN, M
SCHNERMANN, J
MALVIN, RL
KILLEN, PD
BRIGGS, JP
机构
[1] UNIV MICHIGAN,DEPT INTERNAL MED,DIV NEPHROL,1150 W MED CTR DR,1560 MSRBII,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,DEPT PHYSIOL,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,DEPT PATHOL,ANN ARBOR,MI 48109
关键词
JUXTAGLOMERULAR APPARATUS; KIDNEY; GENE EXPRESSION; SODIUM; RATS; INBRED STRAINS;
D O I
10.1161/01.HYP.21.1.36
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Renin secretion responds rapidly to a variety of stimuli; however, reported changes in renal renin messenger RNA (mRNA) levels in vivo have been observed only after prolonged stimulation. Studies were designed to test whether rapid changes in renin mRNA levels can be produced in vivo. In the first series, Sprague-Dawley rats received furosemide (10 mg/kg) intraperitoneally and a low sodium diet (0.05% sodium); renin secretion was significantly stimulated at 8 or 16 hours after treatment, but renin mRNA levels did not change. In a second series, rats were pretreated with deoxycorticosterone acetate (200 mg/kg) and saline drinking water for 3 days and then killed 0, 2, 4, 8, or 48 hours after furosemide administration. The renin mRNA level was unchanged at 2 hours but was stimulated twofold at 4 and 8 hours and threefold at 48 hours. In additional animals, the response of renin mRNA 4 hours after furosemide was found not to be potentiated by the converting enzyme inhibitor quinapril (5 mg/kg). The results demonstrate that with acute stimulation, renin mRNA levels lag 2-4 hours behind the change in plasma renin levels.
引用
收藏
页码:36 / 41
页数:6
相关论文
共 36 条
  • [1] EFFECT OF MINERALOCORTICOIDS AND SALT LOADING ON RENIN RELEASE, RENAL RENIN CONTENT AND RENAL RENIN MESSENGER-RNA IN MICE
    BARRETT, G
    MORGAN, T
    SMITH, M
    ALDRED, P
    [J]. CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1989, 16 (08) : 631 - 639
  • [2] EFFECT OF CONVERTING ENZYME-INHIBITION ON RENIN SYNTHESIS AND SECRETION IN MICE
    BARRETT, GL
    MORGAN, TO
    SMITH, M
    ALCORN, D
    ALDRED, P
    [J]. HYPERTENSION, 1989, 14 (04) : 385 - 395
  • [3] BRIGGS JP, 1991, RENAL PHYSIOL BIOCH, V14, P164
  • [4] MOLECULAR-CLONING OF RAT RENIN CDNA AND ITS GENE
    BURNHAM, CE
    HAWELUJOHNSON, CL
    FRANK, BM
    LYNCH, KR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (16) : 5605 - 5609
  • [5] ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE
    CHIRGWIN, JM
    PRZYBYLA, AE
    MACDONALD, RJ
    RUTTER, WJ
    [J]. BIOCHEMISTRY, 1979, 18 (24) : 5294 - 5299
  • [6] GENOMIC SEQUENCING
    CHURCH, GM
    GILBERT, W
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07): : 1991 - 1995
  • [7] NUMBER AND EVOLUTIONARY CONSERVATION OF ALPHA-TUBULIN AND BETA-TUBULIN AND CYTOPLASMIC BETA-ACTIN AND GAMMA-ACTIN GENES USING SPECIFIC CLONED CDNA PROBES
    CLEVELAND, DW
    LOPATA, MA
    MACDONALD, RJ
    COWAN, NJ
    RUTTER, WJ
    KIRSCHNER, MW
    [J]. CELL, 1980, 20 (01) : 95 - 105
  • [8] COOK CR, 1979, J CLIN INVEST, V49, P1630
  • [9] MOLECULAR-BIOLOGY OF THE RENIN-ANGIOTENSIN SYSTEM
    DZAU, VJ
    BURT, DW
    PRATT, RE
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (04): : F563 - F573
  • [10] FEINBERG A, 1982, ANAL BIOCHEM, V132, P6