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Am J Physiol Gastrointest Liver Physiol 273: G1031-G1035, 1997;
0193-1857/97 $5.00
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Vol. 273, Issue 5, G1031-G1035, November 1997

alpha 1-Acid glycoprotein reduces local and remote injuries after intestinal ischemia in the rat

Julian P. Williams, Martin R. Weiser, Taine T. V. Pechet, Les Kobzik, Francis D. Moore Jr., and Herbert B. Hechtman

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 alpha 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 alpha 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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