Effects of aspirin on atherosclerosis and the cyclooxygenase-2 expression in atherosclerotic rabbits.
- Author:
Yi GUO
1
;
Qi-zhang WANG
;
Bing-shan TANG
;
Yan-fang ZUO
;
Fang-ming LI
;
Xin JIANG
;
Ling WANG
;
Ke-fu MA
Author Information
- Publication Type:Journal Article
- MeSH: Animals; Aorta; pathology; Aspirin; pharmacology; Atherosclerosis; pathology; prevention & control; Cholesterol, Dietary; administration & dosage; Cyclooxygenase 2; analysis; Immunohistochemistry; Lipids; blood; Male; Rabbits
- From: Chinese Medical Journal 2006;119(21):1808-1814
- CountryChina
- Language:English
-
Abstract:
BACKGROUNDAtherosclerosis is a complex vascular inflammatory disease. Aspirin is a mainstay in the prevention of vascular complications of atherosclerosis. In this study, the effectiveness of aspirin in suppressing atherosclerosis and the inflammation process was evaluated in rabbits fed with a high fat diet.
METHODSEighteen male New Zealand rabbits were randomly divided into 3 groups: control group, untreated cholesterol-fed group, aspirin treated cholesterol-fed group, which were fed for 12 weeks. After 12 weeks, the aorta was harvested for pathologic morphology observation. Immunohistochemical analysis of cyclooxygenase-2 (COX-2), macrophage and vascular smooth muscle cell (VSMC) was performed. The statistical analysis was performed by the statistical program SPSS10.0.
RESULTSThe aorta plaque/intima size (P/I) by pathologic morphology observation was 0%, (59.6 +/- 13.7)% and (36.3 +/- 16.5)% in the control, untreated cholesterol-fed group and aspirin treated group, respectively. The maximum plaque thickness, the degree of artery stenosis and the proportion of the intimal circumference occupied by atheroma of the 3 groups were significantly different from each other (P < 0.01). The expression of COX-2 and macrophage in plaque of the aspirin treated group were decreased compared with that in untreated cholesterol-fed group. However, no difference was found in the expression of VSMC between the aspirin treated and the untreated cholesterol-fed group.
CONCLUSIONThe mechanism of atherosclerosis suppression by aspirin in cholesterol-fed rabbits is related to the inhibition of COX-2 expression together with the reduced inflammation followed by, but not related to the hypolipidemic effects.