Abstract | OBJECTIVE: METHODS: Dahl salt sensitive rats fed on 8% NaCl diet from 7 weeks (hypertensive DHF model) were studied at 13 weeks (n=6) or at 19 weeks following chronic administration of a subdepressor dose of temocapril (0.2 mg/kg/day, TEM(+), n=6) or placebo (TEM(-), n=7) from 13 weeks. RESULTS: Compensatory LVH was associated with prolonged time constant of LV relaxation (Tau) at 13 weeks. In TEM(-), progression of LVH and fibrosis and elevation of LV end diastolic pressure were observed at 19 weeks. Administration of temocapril from 13 weeks prevented the further progression of LVH and fibrosis, attenuated increases in myocardial stiffness constant and Tau, and prevented the development of DHF. These effects were accompanied with the attenuation of decreases in sarcoplasmic reticulum calcium(2+)- ATPase 2a and phosphorylated phospholamban and of hypertrophic signalings' upregulation. CONCLUSIONS: This study demonstrated that chronic administration of temocapril exerts a therapeutic effect on diastolic dysfunction and prevents the transition to DHF even if initiated after appearance of LVH and diastolic dysfunction.
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Authors | Yasushi Sakata, Kazuhiro Yamamoto, Toshiaki Mano, Nagahiro Nishikawa, Junichi Yoshida, Takeshi Miwa, Masatsugu Hori, Tohru Masuyama |
Journal | Cardiovascular research
(Cardiovasc Res)
Vol. 57
Issue 3
Pg. 757-65
(Mar 2003)
ISSN: 0008-6363 [Print] England |
PMID | 12618237
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Angiotensin-Converting Enzyme Inhibitors
- Antihypertensive Agents
- Calcium-Binding Proteins
- RNA, Messenger
- Thiazepines
- phospholamban
- temocapril hydrochloride
- Sarcoplasmic Reticulum Calcium-Transporting ATPases
- Calcium-Transporting ATPases
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Topics |
- Angiotensin-Converting Enzyme Inhibitors
(therapeutic use)
- Animals
- Antihypertensive Agents
(therapeutic use)
- Calcium-Binding Proteins
(biosynthesis, genetics)
- Calcium-Transporting ATPases
(biosynthesis, genetics)
- Disease Progression
- Fibrosis
- Gene Expression Regulation
(drug effects)
- Heart Failure
(prevention & control)
- Hemodynamics
- Hypertension
(drug therapy)
- Hypertrophy, Left Ventricular
(drug therapy)
- Male
- RNA, Messenger
(genetics)
- Rats
- Rats, Inbred Dahl
- Reverse Transcriptase Polymerase Chain Reaction
- Sarcoplasmic Reticulum Calcium-Transporting ATPases
- Thiazepines
(therapeutic use)
- Ventricular Function, Left
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