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1-Acid glycoprotein reduces local and
remote injuries after intestinal ischemia in the rat
Department of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115
The aim of this study was to look at the role
of
1-acid glycoprotein as a natural anti-inflammatory
agent with particular respect to its antineutrophil and anticomplement
activity. A recombinantly engineered form of sialyl Lewisx
(sLex)-bearing
1-acid glycoprotein (sAGP)
was administered intravenously to pentobarbital-anesthetized rats after
50 min of intestinal ischemia just before 4 h of reperfusion. A
non-sLex-bearing form of AGP (nsAGP) was used as control.
sAGP-treated animals had a 62% reduction (P < 0.05) in
remote lung injury, assessed by 125I-albumin permeability,
compared with those treated with nsAGP (permeability index of
3.61 ± 0.15 × 10
3 and
5.18 ± 0.67 × 10
3, respectively). There was a
reduction in pulmonary myeloperoxidase levels in sAGP-treated rats
compared with nsAGP-treated rats. Complement-dependent intestinal
injury, assessed by 125I-albumin permeability was reduced
by 28% (P < 0.05) in animals treated with sAGP
(7.58 ± 0.63) compared with those treated with nsAGP
(10.4 ± 0.54). We conclude that sAGP ameliorates both complement- and neutrophil-mediated injuries.
complement; lung; neutrophils; selectins; sialyl Lewisx
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