ET-1 INDUCED BRONCHOCONSTRICTION IN THE EARLY PHASE BUT NOT LATE PHASE OF ANESTHETIZED DOGS IS INHIBITED BY INDOMETHACIN AND ICI-198615

被引:12
作者
UCHIDA, Y
HAMADA, M
KAMEYAMA, M
OHSE, H
NOMURA, A
HASEGAWA, S
HIRATA, F
机构
[1] WAYNE STATE UNIV,DEPT PHARMACEUT SCI,528 SHAPERO HALL,DETROIT,MI 48202
[2] UNIV TSUKUBA,INST CLIN MED,DIV RESP,TSUKUBA,IBARAKI 305,JAPAN
[3] WAYNE STATE UNIV,INST CHEM TOXICOL,DEPT PHARMACOL,DETROIT,MI 48202
关键词
D O I
10.1016/S0006-291X(05)80317-1
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Intratracheally injected or aerosolized ET-1 induced quick and long-lasting bronchoconstriction of anesthetized mongrel dogs, thus increasing respiratory resistance(Rrs) with concomitantly decreasing dynamic compliance(Cdyn). As collateral resistance(Rcs) was measured postexposure to aerosolized ET-1 using wedged bronchoscope technique, ET-1 increased Rcs in a dose and time dependent manner. The increase attained maximal in 2 min and then, gradually declined. When the dogs were pretreated with the intravenous injection of 0.1 μg/kg ICI 198615, an inhibitor of lipoxygenase, the constrictive response was slowed down. Essentially similar results were also observed with the intravenous injection of 5 mg/kg indomethacin. Our observations suggest that the early phase of the ET-1 induced bronchoconstriction is mediated by eicosanoid metabolites. © 1992 Academic Press, Inc.
引用
收藏
页码:1197 / 1202
页数:6
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