LECITHINIZED SUPEROXIDE-DISMUTASE ATTENUATES PHORBOL-MYRISTATE ACETATE-INDUCED INJURY IN ISOLATED DOG LUNG

Citation
T. Miyahara et al., LECITHINIZED SUPEROXIDE-DISMUTASE ATTENUATES PHORBOL-MYRISTATE ACETATE-INDUCED INJURY IN ISOLATED DOG LUNG, European journal of pharmacology, 344(2-3), 1998, pp. 231-239
Citations number
36
Categorie Soggetti
Pharmacology & Pharmacy
ISSN journal
00142999
Volume
344
Issue
2-3
Year of publication
1998
Pages
231 - 239
Database
ISI
SICI code
0014-2999(1998)344:2-3<231:LSAPA>2.0.ZU;2-3
Abstract
Lecithinized superoxide dismutase, a lecithin derivative bound to reco mbinant human CuZn superoxide dismutase, has a higher affinity for cel ls such as polymorphonuclear leukocytes and endothelial cells than rec ombinant human CuZn superoxide dismutase has. We determined the protec tive effects of lecithinized superoxide dismutase on the increased mic rovascular permeability induced by phorbol myristate acetate (PMA) in isolated dog lungs. Microvascular permeability was assessed by the cap illary filtration coefficient (K-f,K-c) and solvent drag reflection co efficient (sigma(f)). PMA (13.3 mu g) increased microvascular permeabi lity, as evidenced by an increase in K-f,K-c and the small sigma(f) va lue. Lecithinized superoxide dismutase at both low (4800 U) and high d oses (48000 U) inhibited the PMA-induced increase in K-f,K-c, but only the high dose of lecithinized superoxide dismutase attenuated the dec rease in sigma(f). Recombinant human CuZn superoxide dismutase did not affect the PMA-induced increase in vascular permeability at either a low (4800 U) or a high dose (48000 U). These findings suggest that lec ithinized superoxide dismutase has a protective effect against oxygen radical-induced lung injury in isolated dogs lungs. (C) 1998 Elsevier Science B.V.