2016 Fiscal Year Final Research Report
Development of a novel therapy for peripartum cardiomyopathy using natriuretic peptides
Project/Area Number |
26461100
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Cardiovascular medicine
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Research Institution | National Cardiovascular Center Research Institute |
Principal Investigator |
OTANI KENTARO 国立研究開発法人国立循環器病研究センター, 研究所, 上級研究員 (50470191)
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Research Collaborator |
KAMIYA CHIZUKO 国立研究開発法人国立循環器病研究センター, 医師 (10551301)
NISHIMURA HIROHITO 国立研究開発法人国立循環器病研究センター研究所, 流動研究員 (30739735)
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Keywords | 周産期心筋症 / ナトリウム利尿ペプチド / 授乳 / 心肥大 |
Outline of Final Research Achievements |
In recent work, we demonstrated that mice lacking guanylyl cyclase-A (GC-A-KO), a receptor for atrial and brain natriuretic peptides, show severe postpartum cardiac hypertrophy. Interestingly, the postpartum cardiac hypertrophy in GC-A-KO was induced during lactation. The aim was to investigate the mechanisms underlying the lactation-induced cardiac hypertrophy in GC-A-KO. Additionally, we examined the single-nucleotide polymorphisms of natriuretic peptide-related genes in patients with peripatrum cardiomyopathy (PPCM). Plasma aldosterone level was significantly elevated in lactating GC-A-KO. Furthermore, the administration of a specific mineralocorticoid receptor blocker during lactation significantly suppressed the cardiac hypertrophy in GC-A-KO. Therefore, aldosterone would be a cause of lactation-induced cardiac hypertrophy in GC-A-KO. In addition, genotype distribution of natriuretic peptide clearance receptor gene differed markedly between women with PPCM and their controls.
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Free Research Field |
循環器内科学
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