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1.
Lipids Health Dis ; 5: 25, 2006 Oct 16.
Article in English | MEDLINE | ID: mdl-17042957

ABSTRACT

BACKGROUND: It has been shown that calcifying vesicles play an important role in aortic calcification and that cholesterol content in the isolated vesicle fraction is increased when rabbits are fed supplemental cholesterol diets. Whether lipoprotein-associated cholesterols and other lipids are also increased in the vesicle fraction and whether the increase correlates with atherosclerosis remain unknown. RESULTS: Fourteen juvenile male rabbits fed an atherogenic diet containing 0.5% cholesterol and 2% peanut oil for 3 months developed varying degrees of hypercholesterolemia and intimal thickening in the ascending thoracic aorta. The correlation between these two parameters was insignificant, and likely attributable to the use of small numbers of rabbits in this study. Despite this lack of correlation, we demonstrate that the accumulation of cholesterol in calcifying vesicle fractions obtained from the collagenase-digested aorta fragments correlates well with intimal thickening (r2 = 0.98, p < 0.0001). To a smaller degree, the correlation was also significant between intimal thickening and the cholesterol accumulation in the microsomal and post-vesicle fractions. The cholesterol supplemental diet increased the low density lipoprotein-cholesterol (LDL-C) content in calcifying vesicle fractions by 3-fold but did not affect the triglyceride content. High density lipoprotein-cholesterol (HDL-C) and very low-density lipoprotein cholesterol (VLD-C) were absent in calcifying vesicle fractions. CONCLUSION: When limited numbers of rabbits are used, LDL-C accumulation in calcifying vesicle fractions is a better biomarker for atherosclerosis than LDL-C levels in the serum. The close association of LDL-C with calcifying vesicles may play an important role in atherosclerosis and calcification.


Subject(s)
Aorta, Thoracic/pathology , Calcinosis/pathology , Cholesterol, Dietary/metabolism , Cholesterol, LDL/metabolism , Cytoplasmic Vesicles/pathology , Tunica Intima/pathology , Animals , Aorta, Thoracic/metabolism , Aortic Diseases/etiology , Aortic Diseases/metabolism , Aortic Diseases/pathology , Biomarkers/metabolism , Calcinosis/metabolism , Cholesterol, Dietary/adverse effects , Coronary Artery Disease/etiology , Coronary Artery Disease/metabolism , Coronary Artery Disease/pathology , Cytoplasmic Vesicles/metabolism , Diet, Atherogenic , Dietary Supplements/adverse effects , Hypercholesterolemia/blood , Male , Microsomes/metabolism , Microsomes/pathology , Rabbits , Tunica Intima/metabolism
2.
Lipids Health Dis ; 5: 16, 2006 Jun 23.
Article in English | MEDLINE | ID: mdl-16796746

ABSTRACT

BACKGROUND: Vascular calcification is implicated in myocardial infarction, instability and rigidity of the aortic wall, and bioprosthetic failures. Although an increase in the calcium (Ca) content in atherogenic diets has been shown to decrease atherosclerosis in rabbits, whether Ca supplementation and deficiency can affect atherosclerosis-related aortic calcification remains unknown. RESULTS: New Zealand White male rabbit littermates were fed an atherogenic diet containing 0.5% cholesterol and 2% peanut oil. The Ca content of the diet, which normally contains 1%, was adjusted to 0.5 or 3%. Segments of thoracic aortas were dissected from rabbits for histological evaluations and Ca and Pi determinations. Rabbits with calcium supplementation were maintained for 4 months, whereas those with calcium deficiency were maintained for 2 1/2 months due to severe icterus beyond this stage. The ratios of intimal to medial areas and calcified to intimal areas were used to semi-quantify lesion accumulation and calcification, respectively. Icterus was estimated from the extent of yellowing of the skin, sclera, and mucous membranes along with gross evidence of hepatic lipidosis and/or biliary obstructions. Statistical analysis of 16 matched littermates shows that Ca supplementation significantly decreased the lesions by 41% (p < 0.05) and markedly inhibited calcification by 62% (p < 0.05). Statistical analysis of 11 matched littermates shows that Ca deficiency significantly increased the lesions by 2.7-fold (p < 0.05) and that the diet caused a small but significant calcification not seen in the sibling groups with normal dietary Ca. Ca supplementation caused a significant 30% decrease in serum cholesterol (p < 0.05). Calcium deficiency increased serum cholesterol by 57% (p < 0.001). Serum cholesterol and LDL-cholesterol levels in Ca deficient rabbits were 2-fold higher than those with high Ca diets. Ca supplementation decreased soluble Ca and Pi content in aortas, suggesting that this effect may underlie the effects of Ca supplementation on calcification. Calcium deficiency increased icterus by 33% (p < 0.05), which may affect hepatic clearance of cholesterol, while calcium supplementation decreased it by 43% (p < 0.001). CONCLUSION: Ca supplementation to an atherogenic diet inhibits atherosclerosis, aortic calcification, and icterus, whereas a Ca deficient-diet promotes them.


Subject(s)
Aortic Diseases/prevention & control , Arteriosclerosis/etiology , Calcinosis/etiology , Calcium, Dietary/therapeutic use , Cholesterol, Dietary/adverse effects , Jaundice/etiology , Animals , Aorta, Thoracic/pathology , Arteriosclerosis/prevention & control , Calcinosis/prevention & control , Calcium/blood , Calcium/deficiency , Diet, Atherogenic , Male , Rabbits
3.
Infect Immun ; 73(10): 7006-10, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16177381

ABSTRACT

Pathophysiological changes associated with anthrax lethal toxin included loss of plasma proteins, decreased platelet count, slower clotting times, fibrin deposits in tissue sections, and gross and histopathological evidence of hemorrhage. These findings suggest that blood vessel leakage and hemorrhage lead to disseminating intravascular coagulation and/or circulatory shock as an underlying pathophysiological mechanism.


Subject(s)
Anthrax/blood , Anthrax/pathology , Antigens, Bacterial/toxicity , Bacterial Toxins/toxicity , Disseminated Intravascular Coagulation/microbiology , Hemorrhage/microbiology , Animals , Anthrax/etiology , Blood Vessels/physiopathology , Bronchi/pathology , Disseminated Intravascular Coagulation/physiopathology , Fibrinogen/analysis , Hemorrhage/pathology , Hemorrhage/physiopathology , Mice , Myocardium/chemistry , Myocardium/pathology
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