FR901451, A NOVEL INHIBITOR OF HUMAN-LEUKOCYTE ELASTASE FROM FLEXIBACTER SP .2. PHARMACOLOGICAL EFFECT OF FR901451

被引:4
作者
FUJITA, T
SHINGUH, Y
YAMAZAKI, A
NAKAHARA, K
OKAMOTO, M
OKUHARA, M
机构
[1] Exploratory Research Laboratories, Fujisawa Pharmaceutical Co. Ltd., Tsukuba, Ibaraki 300-26
关键词
D O I
10.7164/antibiotics.47.1365
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Intratracheal (i.t.) or intravenous (i.v.) administration of FR901451, a potent inhibitor of human leukocyte elastase (HLE) prevented HLE-induced lung hemorrhage in hamsters with ED(50) values of 10.5 mu g/site and 8.1 mg/kg, respectively. alpha 1-Antitrypsin (alpha 1-AT) also showed inhibitory effect in this model. However, the ED(50) value by i.t. injection of FR901451 was 20-fold lower than that of alpha 1-AT. Moreover, FR901451 i.t. significantly modulated porcine pancreas elastase (PPE)-induced changes of the respiratory mechanics in hamsters. The ED(50) values were 529 mu g/site and 244 mu g/site, which were expressed by static lung compliance (Cst) and vital capacity (VC) of the lungs, respectively. These results suggest that FR901451 could be clinically useful agent for the treatment of the destructive lung disease such as pulmonary emphysema.
引用
收藏
页码:1365 / 1368
页数:4
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