Skip to main content
. 2010 Dec 1;4(1):4–16. doi: 10.1007/s12410-010-9060-6

Fig. 3.

Fig. 3

En-face preparations of Sudan-stained aortas from an apoE−/− mouse (a) and a Watanabe heritable hyperlipidemic (WHHL) rabbit (b) injected with 125I-MDA2. Red color (left panels in a and b) signifies the presence of neutral lipid within the atherosclerotic plaque stained with Sudan IV, and black color (right panels in a and b) in the corresponding autoradiograph signifies the presence of accumulated 125I-MDA2 reflecting the presence of MDA-lysine epitopes. Panel C shows the relationship of 125I-MDA2 uptake and plaque burden as measured by aortic weight. A similar relationship is present with percent atherosclerosis surface area. Panels d and e represent in vivo imaging of atherosclerotic WHHL (d) and nonatherosclerotic New Zealand white (e) rabbits with 99mTc-MDA2. (Reprinted with permission from Tsimikas et al. [9], [10•])