Efficacy of different chemical treatments on calcification of vascular
graft in vitro and in vivo was studied. Culture medium-filled rat aor
tas were separately treated in 0.2% glutaraldehyde and epoxy compound,
and photooxidized in 0.01% methylene blue for a shorter period (group
1). Another group of rat aortas were separately treated in the same c
hemicals for a longer period (group 2). All fresh and treated aortas o
f both groups were cultured for 21 days in an organ culture medium and
implanted (except for group 1) in weanling rats for five months. Hist
ology and immunohistochemistry revealed that differently treated aorta
s of group 1 grow and calcify, and the smooth muscle cells between ela
stin fibers are the primary site of calcium deposition. In contrast, d
ifferently treated aortas of group 2 neither grew, nor did calcify in
the medium except the epoxy compound cross-linked aorta of group 2 whi
ch did not grow but did calcify. Untreated aorta did not calcify. All
fresh and differently treated aortic homografts calcified severely in
rats. Our whole arterial segment-calcification system would be useful
for analyzing the molecular and cellular mechanisms of both bioprosthe
tic and atherosclerotic calcification of vascular graft. New anticalci
fication technique is the only hope for better outcome of future vascu
lar bioprostheses. (C) 1998 Published by Elsevier Science Ltd. All rig
hts reserved.