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Fatty acid bile acid conjugates inhibit atherosclerosis in the C57BL/6 mouse model.
- Source :
-
Pathobiology : journal of immunopathology, molecular and cellular biology [Pathobiology] 2002-2003; Vol. 70 (4), pp. 215-8. - Publication Year :
- 2002
-
Abstract
- Objective: The aim of the current research was to study whether fatty acid bile acid conjugates (FABACs) have a beneficial effect on atherosclerosis progression and blood lipid levels in mice.<br />Methods: C57BL/6 female mice, fed a high-fat Paigen diet, were administered an oral dose of FABAC or DDH2O daily. Quantification of atherosclerotic fatty-streak lesions at the aortic sinus was performed.<br />Results: The FABAC-treated mice showed a significant reduction in the atherosclerotic lesion areas as compared to the control group (p = 0.019). A significant elevation in total cholesterol levels was observed in both the FABAC and control groups. Higher FABAC levels were measured in the high-density lipoprotein fraction as compared to the very-low-density and low-density lipoprotein fractions.<br />Conclusion: Our findings demonstrate that FABACs, given orally, reduce the development of atherosclerosis in mice fed a high-fat high-cholesterol diet, despite a lack of effect on plasma lipid levels.<br /> (Copyright 2003 S. Karger AG, Basel)
- Subjects :
- Administration, Oral
Animals
Arteriosclerosis blood
Arteriosclerosis pathology
Bile Acids and Salts administration & dosage
Body Weight drug effects
Cholesterol blood
Cholesterol classification
Diet, Atherogenic
Disease Models, Animal
Disease Progression
Fatty Acids administration & dosage
Female
Mice
Mice, Inbred C57BL
Sinus of Valsalva drug effects
Sinus of Valsalva pathology
Triglycerides blood
Arteriosclerosis prevention & control
Bile Acids and Salts pharmacology
Fatty Acids pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1015-2008
- Volume :
- 70
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Pathobiology : journal of immunopathology, molecular and cellular biology
- Publication Type :
- Academic Journal
- Accession number :
- 12679599
- Full Text :
- https://doi.org/10.1159/000069332