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Rev Port Cardiol ; 36(9): 629-638, 2017 Sep.
Article in English, Portuguese | MEDLINE | ID: mdl-28826937

ABSTRACT

INTRODUCTION AND OBJECTIVE: Dyslipidemia is associated with increased risk of cardiovascular disease and atherosclerosis, and hence with high morbidity and mortality. This study investigated the effects of the nitroxide 4-hydroxy-2,2,6,6-tetramethylpiperidine 1-oxyl (Tempol) on lipid profile and cardiac morphology in low-density lipoprotein (LDL) receptor gene knockout (LDLr-/-) mice. METHODS: Male LDLr-/- mice (three months old, approximately 22 g weight) were divided into the following groups: controls, including (1) standard chow (SC, n=8) and (2) high-fat diet (HFD, n=8); and treatment, including (3) standard chow + Tempol (SC+T, n=8) (30 mg/kg administered by gavage, once daily) and (4) high-fat diet + Tempol (HFD+T, n=8) (30 mg/kg). After 30 days of the diet/treatment, whole blood was collected for analysis of biochemical parameters (total cholesterol, triglycerides [TG], high-density lipoprotein [HDL], LDL, and very low-density lipoprotein [VLDL]). The heart was removed through thoracotomy and histological analysis of the left ventricle was performed. RESULTS: A significant increase in TG, LDL, and VLDL and marked left ventricular hypertrophy (LVH) were demonstrated in the HFD group relative to the SC group (p<0.05), while Tempol treatment (HFD+T group) significantly (p<0.05) prevented increases in the levels of these lipid profile markers and attenuated LVH compared with the HFD group. CONCLUSION: In this study, Tempol showed potential for the prevention of events related to serious diseases of the cardiovascular system.


Subject(s)
Cyclic N-Oxides/pharmacology , Cyclic N-Oxides/therapeutic use , Diet, High-Fat , Hypertrophy, Left Ventricular/prevention & control , Lipid Metabolism/drug effects , Animals , Lipids/blood , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Receptors, LDL/genetics , Spin Labels
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