ANTIINFLAMMATORY EFFECT OF THE CONJUGATE OF SUPEROXIDE-DISMUTASE WITHTHE COPOLYMER OF DIVINYL ETHER AND MALEIC-ANHYDRIDE AGAINST RAT REEXPANSION PULMONARY-EDEMA

Citation
T. Hirano et al., ANTIINFLAMMATORY EFFECT OF THE CONJUGATE OF SUPEROXIDE-DISMUTASE WITHTHE COPOLYMER OF DIVINYL ETHER AND MALEIC-ANHYDRIDE AGAINST RAT REEXPANSION PULMONARY-EDEMA, Journal of controlled release, 48(2-3), 1997, pp. 131-139
Citations number
36
Categorie Soggetti
Pharmacology & Pharmacy",Chemistry
ISSN journal
01683659
Volume
48
Issue
2-3
Year of publication
1997
Pages
131 - 139
Database
ISI
SICI code
0168-3659(1997)48:2-3<131:AEOTCO>2.0.ZU;2-P
Abstract
Bovine erythrocyte superoxide dismutase (SOD) was conjugated with the copolymer of divinyl ether and maleic anhydride, known as DIVEMA or py ran copolymer. The DM-SOD conjugate was resistant against the proteoly tic enzymes in serum, and showed a prolonged half-life in vivo after i ntravenous injection. DM-SOD was applied for the treatment of rat lung edema caused by the re-expansion after the left bronchus has been cli pped for 3 days. The anti-inflammatory effect was evaluated by the inh ibition rate of the water content due to the edema. Neither SOD nor DI VEMA reduced the increase in water content in the lung, whereas DM-SOD could effectively protect against the increase in water content such that the water content of the re-expanded lung was the same as that of the control right lung. Using electron microscopic observation the di fference between the SOD and DM-SOD treatment in the water swelling of the interalveolar septum was clearly indicated. Observation of the su rface of the endothelial wall in the blood vessel of the lung showed m ore a drastic difference. The leukocyte attachment on the endothelial layer observed following the treatment with SOD was not observed follo wing that with DM-SOD. This observation indicates that DM-SOD had stop ped the inflammation process at the first step of leukocyte adhesion, which should be followed by the rolling and expansion of the leukocyte s to initiate the normal inflammation process. (C) 1997 Elsevier Scien ce B.V.