Preventing progression of cardiac hypertrophy and development of heart failure by paricalcitol therapy in rats

被引:61
|
作者
Bae, Soochan [2 ]
Yalamarti, Bhargavi [2 ]
Ke, Qingen [2 ]
Choudhury, Sangita [2 ]
Yu, Hyeon [2 ,3 ]
Karumanchi, S. Ananth [4 ,5 ]
Kroeger, Paul [6 ]
Thadhani, Ravi [1 ]
Kang, Peter M. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Div Nephrol, Boston, MA 02114 USA
[2] Beth Israel Deaconess Med Ctr, Div Cardiovasc, Boston, MA 02215 USA
[3] Chonbuk Natl Univ, Dept BIN Fus Technol, Jeonju, South Korea
[4] Beth Israel Deaconess Med Ctr, Div Nephrol, Boston, MA 02215 USA
[5] Beth Israel Deaconess Med Ctr, Howard Hughes Med Inst, Boston, MA 02215 USA
[6] Abbott Labs, Abbott Pk, IL 60064 USA
基金
美国国家卫生研究院;
关键词
Dahl rats; ACE inhibitor; BNP; Fibrosis; Microarrays; VITAMIN-D DEFICIENCY; RENIN-ANGIOTENSIN SYSTEM; KINASE-C BETA; D-RECEPTOR; CARDIOVASCULAR-DISEASE; 1,25-DIHYDROXYVITAMIN D-3; EXPRESSION; APOPTOSIS; OVEREXPRESSION; PROLIFERATION;
D O I
10.1093/cvr/cvr133
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims Vitamin D deficiency is associated with cardiac hypertrophy and heart failure, and vitamin D therapy prevents the progression of cardiac hypertrophy in animal models. Here, we examine whether vitamin D therapy prevents progression of pre-existing cardiac hypertrophy and development of heart failure. Methods and results When male Dahl salt-sensitive rats were fed a high salt (HS) diet, all rats developed cardiac hypertrophy after 5 weeks. Thereafter, rats were treated with vehicle (V), paricalcitol (PC, an active vitamin D analogue, at 200 ng, IP 3x/week), enalapril (EP, 90 mu g/day), and PC + EP. All groups were continued on the HS diet and evaluated after 4 weeks of therapy. The PC and PC + EP groups, but not the V and EP only groups, showed significant prevention of progression of pre-existing cardiac hypertrophy. The signs of decompensated heart failure were evident in the vehicle-treated group; these heart failure parameters significantly improved with PC, EP or PC + EP therapy. The expression of PKC alpha, which is regulated by Ca(2+) and known to stimulate cardiac hypertrophy, was significantly increased in the vehicle group, and PC, EP or PC + EP effectively decreased PKC alpha activation. We also observed normalization of genetic alterations during progression to heart failure with PC treatment. Conclusion PC treatment resulted in both the prevention of progression of pre-existing cardiac hypertrophy and the development of heart failure, compared with improvement in progression to heart failure by EP alone. These beneficial findings in heart were associated with inhibition of PKC alpha activation and reversal of gene alterations.
引用
收藏
页码:632 / 639
页数:8
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