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Arteriosclerosis, Thrombosis, and Vascular Biology. 1997;17:10-17

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(Arteriosclerosis, Thrombosis, and Vascular Biology. 1997;17:10-17.)
© 1997 American Heart Association, Inc.


Articles

Influence of Hypercholesterolemia and Adventitial Inflammation on the Development of Aortic Aneurysm in Rabbits

T. Freestone; R.J. Turner; D.J. Higman; M.J. Lever; J.T. Powell

the Departments of Biochemistry (T.F., R.J.T., J.T.P.) and Surgery (D.J.H., J.T.P.), Charing Cross and Westminster Medical School, and Imperial College (M.J.L.), London, UK.

Correspondence to J.T. Powell, Department of Surgery, Charing Cross Hospital, Fulham Palace Road, London W6 8RF, UK.

Abdominal aortic aneurysms are characterized by intimal atherosclerosis, disruption and attenuation of the elastic media, and a variable adventitial inflammatory infiltrate. We have developed an animal model of this disorder to evaluate the contribution of hypercholesterolemia, medial injury, and adventitial inflammation to aneurysmal dilatation. To accomplish this, we used periaortic application of calcium chloride, which induced both medial injury with calcification and endothelial injury. Ultrasonography was used to demonstrate the dilatation and thickening of the aortic wall. Over the first 3 weeks after periaortic application of 0.25 mol/L CaCl2, the external aortic diameter increased from 3.5±0.5 to 4.2±0.8 mm, but the ID remained unchanged. This apparent wall thickening was accompanied by vascular remodeling, and biochemical changes included {approx}50% reduction in tissue hydroxyproline concentration and increased activity of gelatinases (matrix metalloproteinase [MMP]-2 and MMP-9). Independently, cholesterol feeding to induce hypercholesterolemia or the concomitant periaortic application of thioglycollate had little effect on the histological, biochemical, or diameter changes. Together, hypercholesterolemia and thioglycollate were associated with rapid aortic dilatation in CaCl2-treated animals but not controls: after 3 weeks, the ID and OD had doubled, the OD increasing from 3.5±0.4 to 7.1±0.4 mm, P=.005. The remarkable feature that accompanied this dilatation was the infiltration of cells, mostly foamy macrophages, into the adventitia, with a further reduction in hydroxyproline concentration. Adventitial inflammation may provide the critical stimulus to dilatation of an aorta with preexisting intimal and medial injury.


Key Words: aneurysm • macrophages • cholesterol • calcification • collagen




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