AORTIC CALCIFICATION PRODUCED BY VITAMIN-D-3 PLUS NICOTINE

Citation
N. Niederhoffer et al., AORTIC CALCIFICATION PRODUCED BY VITAMIN-D-3 PLUS NICOTINE, Journal of vascular research, 34(5), 1997, pp. 386-398
Citations number
32
Categorie Soggetti
Peripheal Vascular Diseas",Physiology
ISSN journal
10181172
Volume
34
Issue
5
Year of publication
1997
Pages
386 - 398
Database
ISI
SICI code
1018-1172(1997)34:5<386:ACPBVP>2.0.ZU;2-Q
Abstract
Calcification of the elastic arteries of the young rat by treatment wi th vitamin D and nicotine (VDN) has been proposed as an animal model o f arterial calcification associated with age and age-related vascular pathology in man. The calcium-binding protein, S-100, which is found i n human atherosclerotic lesions was associated with medial calcificati on of the aorta in VDN rats, especially in cases of severe calcificati on. Calcification (total calcium content: 366 +/- 87, n = 12 in VDN vs . 24 +/- 2 mu mol g(-1) aortic dry weight in controls, n = 13) involve d elastocalcinosis leading to elastolysis as revealed by a fall in the amount of desmosine and isodesmosine in the aortic wall (266 +/- 17 a nd 254 +/- 15 in VDN vs. 655 +/- 56 and 588 +/- 30 mu g g(-1) aortic d ry weight in controls). The decrease in elastin was associated with an increase in the stiffness of the aortic wall (elastic modulus: 15.1 /- 1.8 in VDN vs. 6.7 +/- 0.5 10(6) dyn cm(-2) in controls), an increa se in end-systolic stress (central systolic aortic pressure: 152 +/- 6 in VDN vs. 136 +/- 2 mm Hg in controls) (at a normotensive mean press ure level) and left ventricular hypertrophy (heart weight/body weight 2.51 +/- 0.10 in VDN vs. 2.24 +/- 0.07 g kg(-1) in controls). In concl usion, the mechanisms and consequences of aortic calcification in VDN show several similarities with calcification occurring in human athero - and arteriosclerosis.