Effects of Low-Dose Sacubitril/Valsartan on Different Stages of Cardiac Hypertrophy in Salt-Loaded Hypertensive Rats.


Journal

Journal of cardiovascular pharmacology
ISSN: 1533-4023
Titre abrégé: J Cardiovasc Pharmacol
Pays: United States
ID NLM: 7902492

Informations de publication

Date de publication:
05 2019
Historique:
pubmed: 5 3 2019
medline: 19 5 2020
entrez: 5 3 2019
Statut: ppublish

Résumé

Sacubitril/valsartan was shown to attenuate the development of cardiac hypertrophy with enhanced blood pressure reduction compared with valsartan alone in animal models. We investigated whether a low-dose sacubitril/valsartan has blood pressure-independent effects on cardiac hypertrophy and pulmonary edema using a rat model of hypertension and obesity. In plan 1, male SHR/NDmcr-cp rats fed normal or phase-increased high salt were treated with vehicle, 6-mg/kg sacubitril/valsartan or 3-mg/kg valsartan, for 6 months. In plan 2, after high-salt loading for 6 months, drugs were administered for 4 months. Antihypertensive effects of the 2 drugs were similar during all study periods. In plan 1 with normal salt, there were no differences between treatments in the left ventricle weight/body weight (BW), or lung weight/BW as an index of cardiac hypertrophy or pulmonary edema, respectively. These indexes were smaller in high-salt-fed rats with sacubitril/valsartan than vehicle. In plan 2, both indexes did not differ between vehicle and sacubitril/valsartan. Ventricle weight/BW was lower in valsartan than sacubitril/valsartan. In plan 2, gene markers of cardiac dysfunction were upregulated by sacubitril/valsartan compared with the other groups. Low-dose sacubitril/valsartan may have different effects depending on the stage of cardiac hypertrophy in rats.

Sections du résumé

BACKGROUND
Sacubitril/valsartan was shown to attenuate the development of cardiac hypertrophy with enhanced blood pressure reduction compared with valsartan alone in animal models. We investigated whether a low-dose sacubitril/valsartan has blood pressure-independent effects on cardiac hypertrophy and pulmonary edema using a rat model of hypertension and obesity.
METHODS AND RESULTS
In plan 1, male SHR/NDmcr-cp rats fed normal or phase-increased high salt were treated with vehicle, 6-mg/kg sacubitril/valsartan or 3-mg/kg valsartan, for 6 months. In plan 2, after high-salt loading for 6 months, drugs were administered for 4 months. Antihypertensive effects of the 2 drugs were similar during all study periods. In plan 1 with normal salt, there were no differences between treatments in the left ventricle weight/body weight (BW), or lung weight/BW as an index of cardiac hypertrophy or pulmonary edema, respectively. These indexes were smaller in high-salt-fed rats with sacubitril/valsartan than vehicle. In plan 2, both indexes did not differ between vehicle and sacubitril/valsartan. Ventricle weight/BW was lower in valsartan than sacubitril/valsartan. In plan 2, gene markers of cardiac dysfunction were upregulated by sacubitril/valsartan compared with the other groups.
CONCLUSIONS
Low-dose sacubitril/valsartan may have different effects depending on the stage of cardiac hypertrophy in rats.

Identifiants

pubmed: 30829732
doi: 10.1097/FJC.0000000000000662
doi:

Substances chimiques

Aminobutyrates 0
Angiotensin II Type 1 Receptor Blockers 0
Biomarkers 0
Biphenyl Compounds 0
Drug Combinations 0
Protease Inhibitors 0
Sodium Chloride, Dietary 0
Tetrazoles 0
Valsartan 80M03YXJ7I
Neprilysin EC 3.4.24.11
sacubitril and valsartan sodium hydrate drug combination WB8FT61183

Types de publication

Comparative Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

282-289

Auteurs

Go Hamano (G)

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Koichi Yamamoto (K)

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Yoichi Takami (Y)

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Hikari Takeshita (H)

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Takashi Shimosato (T)

Research Department, NISSEI BILIS Co, Ltd, Shiga, Japan.

Toshinori Moritani (T)

Research Department, NISSEI BILIS Co, Ltd, Shiga, Japan.

Hiromi Rakugi (H)

Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

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Classifications MeSH