SUSCEPTIBILITY TO ATHEROSCLEROSIS IN MICE EXPRESSING EXCLUSIVELY APOLIPOPROTEIN B48 OR APOLIPOPROTEIN B100

Citation
Mm. Veniant et al., SUSCEPTIBILITY TO ATHEROSCLEROSIS IN MICE EXPRESSING EXCLUSIVELY APOLIPOPROTEIN B48 OR APOLIPOPROTEIN B100, The Journal of clinical investigation, 100(1), 1997, pp. 180-188
Citations number
34
Categorie Soggetti
Medicine, Research & Experimental
ISSN journal
00219738
Volume
100
Issue
1
Year of publication
1997
Pages
180 - 188
Database
ISI
SICI code
0021-9738(1997)100:1<180:STAIME>2.0.ZU;2-K
Abstract
All classes of lipoproteins considered to be atherogenic contain apo-B 100 or apo-B48, However. there is a distinct paucity of data regarding whether lipoproteins containing apo-B48 or apo-B100 differ in their i ntrinsic ability to promote the development of atherosclerosis, To add ress this issue, we compared the extent of atherosclerosis in three gr oups of animals: apo-E-deficient mice (apo-B(+/+)apo-E-/-) and apoE-de ficient mice that synthesize exclusively either apo-B48 (apo-B(48/48)a po-E-/-) or apo-B100 (apo-B(100/100)apo-E-/-). Mice (n = 25 in each gr oup) were fed a chow diet for 300 days, and plasma lipid levels were a ssessed throughout the study, Compared with the levels in apo-B(+/+)ap o-E-/- mice, the total plasma cholesterol levels were higher in the ap oB(100/100)apo-E-/- mice and were lower in the apo-B(48/48)apoE(-/-) m ice, However, the ranges of cholesterol levels in the three groups ove rlapped. Compared with those in the apo-B(+/+)po-E-/- mice, atheroscle rotic lesions were more extensive in the apo-B-48/48-E-/- mice and les s extensive in the apo-B(100/100)apo-E-/- mice, Once again, however, t here was overlap among the three groups, The extent of atherosclerosis in each group of mice correlated significantly with plasma cholestero l levels, In mice from different groups that had similar cholesterol l evels. the extent of atherosclerosis was quite similar, Thus, suscepti bility to atherosclerosis was dependent on total cholesterol levels, W hether mice synthesized apo-B48 or apo-B100 did not appear to have an independent effect on susceptibility to atherosclerosis.