Regression of myocardial fibrosis in hypertensive heart disease: diverse effects of various antihypertensive drugs

被引:71
作者
Brilla, CG [1 ]
机构
[1] Univ Marburg, Div Cardiol, Ctr Internal Med, D-35033 Marburg, Germany
关键词
ACE inhibitors; adrenergic (ant)agonists; antihypertensive agents; fibrosis; hypertension; hypertrophy;
D O I
10.1016/S0008-6363(99)00432-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: In left ventricular hypertrophy (LVH) due to systemic hypertension, myocardial fibrosis is an important determinant of pathologic hypertrophy. Therefore, it is most relevant to utilize an antihypertensive regimen that permits a regression in myocardial fibrosis along with blood pressure normalization and regression of LVH. Methods: To address this issue we examined 60 Sprague-Dawley rats. We treated 16-week-old rats having established LVH and myocardial fibrosis due to 8-week renovascular hypertension (RHT) with either 6 mg/kg/day zofenopril (ZOF), 30 mg/kg/day nifedipine (NIF) or 40 mg/kg/day labetalol (LAB) for 12 weeks. Systolic arterial pressure (SAP, mmHg), left ventricular/body weight ratio (LV/BW, mg/g), and left and right ventricular collagen volume fractions (LVCVF, RVCVF, %) were obtained and compared with age/sex matched untreated rats with RHT and sham-operated controls. Results: In RHT, SAP was significantly elevated compared with controls (188+/-11 vs. 125+/-5 mmHg; P<0.001) while in each treated group SAP was normalized. LV/BW was significantly increased in RHT (2.61+/-0.12 mg/g; P<0.00001) while in each treated group LVH was completely regressed (P<0.002 vs. untreated RHT) with LV/BW values comparable to controls (1.83+/-0.03 mg/g) irrespective of the utilized antihypertensive agent. In untreated RHT, myocardial fibrosis was present in the left (LVCVF: 12.3+/-1.9%: P<0.0005 vs. 4.5+/-0.2% of controls) and right ventricles (RVCVF: 20.6+/-2.5%; P<0.00005 vs. 8.8+/-0.4% of controls). In rats treated with ZOF or NIF, LVCVF was significantly reduced to 5.6+/-0.4 and 5.4+/-0.6%, respectively (P<0.005 vs. untreated RHT), and RVCVF was decreased as well (ZOF: 11.0+/-0.9%; NIF: 10.4+/-2.4%: P<0.007 vs, untreated RHT) where: no significant difference to controls remained. In contrast. treatment with LAB did not affect myocardial fibrosis where LVCVF was 9.3+/-1.3% and RVCVF was 19.8+/-2.8%. i.e., remained significantly elevated compared with controls (P<0.007). Conclusions: In rats with renovascular hypertension and hypertensive heart disease that included LVH and fibrosis, equipotent doses of ZOF, NIF, and LAB normalized arterial pressure associated with regression of LVH while only ZOF and NIF were found to regress myocardial fibrosis. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:324 / 331
页数:8
相关论文
共 65 条
  • [1] EFFECTS OF NIFEDIPINE AND MOXONIDINE ON CARDIAC STRUCTURE IN SPONTANEOUSLY HYPERTENSIVE RATS - STEREOLOGICAL STUDIES ON MYOCYTES, CAPILLARIES, ARTERIES, AND CARDIAC INTERSTITIUM
    AMANN, K
    GREBER, D
    GHAREHBAGHI, H
    WIEST, G
    LANGE, B
    GANTEN, U
    MATTFELDT, T
    MALL, G
    [J]. AMERICAN JOURNAL OF HYPERTENSION, 1992, 5 (02) : 76 - 83
  • [2] HISTO-PATHOLOGICAL TYPES OF CARDIAC FIBROSIS IN MYOCARDIAL-DISEASE
    ANDERSON, KR
    SUTTON, MGS
    LIE, JT
    [J]. JOURNAL OF PATHOLOGY, 1979, 128 (02) : 79 - &
  • [3] BARTOSOVA D, 1969, J PHYSIOL-LONDON, V200, P185
  • [4] REGULATION OF COLLAGEN PRODUCTION BY THE BETA-ADRENERGIC SYSTEM
    BERG, RA
    MOSS, J
    BAUM, BJ
    CRYSTAL, RG
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1981, 67 (05) : 1457 - 1462
  • [5] ALTERATIONS IN CARDIAC GENE-EXPRESSION DURING THE TRANSITION FROM STABLE HYPERTROPHY TO HEART-FAILURE - MARKED UP-REGULATION OF GENES ENCODING EXTRACELLULAR-MATRIX COMPONENTS
    BOLUYT, MO
    ONEILL, L
    MEREDITH, AL
    BING, OHL
    BROOKS, WW
    CONRAD, CH
    CROW, MT
    LAKATTA, EG
    [J]. CIRCULATION RESEARCH, 1994, 75 (01) : 23 - 32
  • [6] BOUCEK RJ, 1973, P SOC EXP BIOL MED, V144, P929
  • [7] ANTI-ALDOSTERONE TREATMENT AND THE PREVENTION OF MYOCARDIAL FIBROSIS IN PRIMARY AND SECONDARY HYPERALDOSTERONISM
    BRILLA, CG
    MATSUBARA, LS
    WEBER, KT
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1993, 25 (05) : 563 - 575
  • [8] Brilla CG, 1999, CIRCULATION, V100, P362
  • [9] REACTIVE AND REPARATIVE MYOCARDIAL FIBROSIS IN ARTERIAL-HYPERTENSION IN THE RAT
    BRILLA, CG
    WEBER, KT
    [J]. CARDIOVASCULAR RESEARCH, 1992, 26 (07) : 671 - 677
  • [10] CARDIOREPARATIVE EFFECTS OF LISINOPRIL IN RATS WITH GENETIC-HYPERTENSION AND LEFT-VENTRICULAR HYPERTROPHY
    BRILLA, CG
    JANICKI, JS
    WEBER, KT
    [J]. CIRCULATION, 1991, 83 (05) : 1771 - 1779