Influence of daidzein on left ventricular remodeling in rats with hypertrophic myocardium induced by pressure overload.
- Author:
Li ZHOU
1
;
Qing ZHOU
;
Xiao-qing XIONG
;
Jian-xin LIU
;
Wei HE
Author Information
- Publication Type:Journal Article
- MeSH: Angiotensin II; blood; metabolism; Animals; Hypertrophy, Left Ventricular; metabolism; pathology; Isoflavones; pharmacology; Male; Myocardium; metabolism; pathology; Nitric Oxide; metabolism; Phytoestrogens; pharmacology; Random Allocation; Rats; Rats, Wistar; Ventricular Remodeling; drug effects
- From: China Journal of Chinese Materia Medica 2007;32(14):1449-1452
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVETo investigate the protective effects of daidzein (DD) on ventricular remodeling in rats with myocardial hypertrophy induced by pressure overload and its mechanism.
METHODMyocardial hypertrophy model of rats induced by pressure overload was prepared by constricting abdominal aorta. The operated rats were randomly divided into sham operated control group, aorta-constricted model group and three DD groups (30, 60, 120 mg kg(-1)). Four weeks later, the heart-weight (HW), left ventricular weight (LVW), the ratio of HW/BW and LVW/BW (LVI) and the cardio-myocyte diameters (MD) after dyeing by HE colar were measured. The hydroxyroline, nitric oxide (NO) and the activity of nitric oxide synthetase (NOS) and Na+ -K+ -ATPase, Ca2+ -ATPase in left ventricle were quantified with spectrophotometry and the angiotension II (Ang II) in left ventricle and serum was messured with radioimmunoassay.
RESULTAfter treatment of the left ventricular with DD, vs aorta-contricted model group, NO content, cNOS and Na+ -K+ -ATPase, Ca2+ -ATPase activity were significantly increased, the content of AngII in left ventricle and serum and iNOS activity and the ratio of HW/BW, LVI, MD were significantly reduced.
CONCLUSIONDD has protective effects on ventricular remodeling in rats with myocardial hypertrophy induced by pressure overload and its mechanism may be related to raising NO content and reducing the level of Ang II.