Journal
CARDIOVASCULAR RESEARCH
Volume 91, Issue 4, Pages 632-639Publisher
OXFORD UNIV PRESS
DOI: 10.1093/cvr/cvr133
Keywords
Dahl rats; ACE inhibitor; BNP; Fibrosis; Microarrays
Categories
Funding
- National Institutes of Health [RO1 HL091998]
- Ministry of Education, Science and Technology, South Korea [R31-20029]
- Abbott Laboratories
- Howard Hughes Medical Institute
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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.
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