Analogs of 1α,25-dihydroxyvitamin D3 as novel inhibitors of renin biosynthesis

被引:65
作者
Qiao, GL
Kong, J
Uskokovic, M
Li, YC
机构
[1] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[2] BioXell Inc, Nutley, NJ 07110 USA
关键词
Vitamin D; Vitamin D analogs; Gemini compounds; renin; renin-angiotensin system; renin inhibitor; As4.1; cells;
D O I
10.1016/j.jsbmb.2005.02.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The renin-angiotensin system (RAS) plays a central role in the pathogenesis of hypertension. Recently, we discovered that 1 alpha,25dihydroxyvitamin D-3 [1,25(OH)(2)D-3] functions as a negative endocrine regulator of renin biosynthesis, which provides a molecular basis to explore the potential of Vitamin D analogs as renin inhibitors to control the RAS. To search for renin-inhibiting Vitamin D analogs, we screened 20 Vitamin D analog compounds using As4.1 -hVDR cell (a juxtaglomerular cell line) culture by Northern blot and luciferase reporter assays. We found that the Gemini compounds, which have two side-chains at carbon-20 position, were particularly active in suppressing renin expression. Eight Gemini compounds were identified that were equally or 10- to 100-times more potent than 1,25(OH)2D3 in renin inhibition. These Gemini compounds also potently stimulate 25-hydroxyvitamin D 24-hydroxylase expression in As4. 1 -hVDR cells. Administration of compound RO-27-5646 [1,25-dihydroxy-21-(3-methyl-3-hydroxy-butyl)-19-nor-cholecalciferol] in mice caused a marked reduction in renal renin mRNA expression without invoking severe hypercalcemia as seen in 1,25(OH)2D3 treatment. These data establish in principle that Vitamin D analogs can indeed inhibit renin expression in vitro and in vivo, and support the notion that low calcemic Vitamin D analogs can potentially be used as therapeutic agents to control the RAS. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:59 / 66
页数:8
相关论文
共 36 条
[1]   Initial treatment of hypertension [J].
August, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (07) :610-617
[2]  
Ballermann BJ, 1991, KIDNEY, P510
[3]   Angiotensin receptors: signaling, vascular pathophysiology, and interactions with ceramide [J].
Berry, C ;
Touyz, R ;
Dominiczak, AF ;
Webb, RC ;
Johns, DG .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2001, 281 (06) :H2337-H2365
[4]   Vitamin D analogues for secondary hyperparathyroidism [J].
Brown, AJ ;
Dusso, AS ;
Slatopolsky, E .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2002, 17 :10-19
[5]   ESSENTIAL HYPERTENSION - RENIN AND ALDOSTERONE, HEART ATTACK AND STROKE [J].
BRUNNER, HR ;
BUHLER, FR ;
BARD, RH ;
BAER, L ;
GOODWIN, FT ;
NEWTON, MA ;
KRAKOFF, LR ;
LARAGH, JH .
NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (09) :441-+
[6]   SPECIFIC-INHIBITION OF RENIN BY AN ANGIOTENSINOGEN ANALOG - STUDIES IN SODIUM DEPLETION AND RENIN-DEPENDENT HYPERTENSION [J].
BURTON, J ;
CODY, RJ ;
HERD, JA ;
HABER, E .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (09) :5476-5479
[7]   Regulation of calbindin-D9k expression by 1,25-dihydroxyvitamin D3 and parathyroid hormone in mouse primary renal tubular cells [J].
Cao, LP ;
Bolt, MJG ;
Wei, MJ ;
Sitrin, MD ;
Li, YC .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 400 (01) :118-124
[8]   RENIN-SPECIFIC ANTIBODY FOR STUDY OF CARDIOVASCULAR HOMEOSTASIS [J].
DZAU, VJ ;
KOPELMAN, RI ;
BARGER, AC ;
HABER, E .
SCIENCE, 1980, 207 (4435) :1091-1093
[9]   MILD HIGH-RENIN ESSENTIAL HYPERTENSION - NEUROGENIC HUMAN HYPERTENSION [J].
ESLER, M ;
JULIUS, S ;
ZWEIFLER, A ;
RANDALL, O ;
HARBURG, E ;
GARDINER, H ;
DEQUATTRO, V .
NEW ENGLAND JOURNAL OF MEDICINE, 1977, 296 (08) :405-411
[10]   Clinical epidemiology of cardiovascular disease in chronic renal disease [J].
Foley, RN ;
Parfrey, PS ;
Sarnak, MJ .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1998, 32 (05) :S112-S119