Effects of Low-Dose Sacubitril/Valsartan on Different Stages of Cardiac Hypertrophy in Salt-Loaded Hypertensive Rats.
Aminobutyrates
/ administration & dosage
Angiotensin II Type 1 Receptor Blockers
/ administration & dosage
Animals
Biomarkers
/ blood
Biphenyl Compounds
Blood Pressure
/ drug effects
Cardiomegaly
/ metabolism
Disease Models, Animal
Drug Combinations
Gene Expression Regulation
Kidney
/ physiopathology
Male
Neprilysin
/ antagonists & inhibitors
Protease Inhibitors
/ administration & dosage
Pulmonary Edema
/ metabolism
Rats, Inbred SHR
Sodium Chloride, Dietary
Tetrazoles
/ administration & dosage
Valsartan
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
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