I-125 ENDOTHELIN-1 AND I-125 BIG ENDOTHELIN-1 IN RAT-TISSUES - AUTORADIOGRAPHIC LOCALIZATION AND RECEPTOR-BINDING

被引:20
|
作者
NEUSER, D
STEINKE, W
DELLWEG, H
KAZDA, S
STASCH, JP
机构
[1] BAYER AG,INST BIOCHEM,W-5600 WUPPERTAL,GERMANY
[2] BAYER AG,INST PHARMACOKINET,W-5600 WUPPERTAL,GERMANY
关键词
D O I
10.1007/BF00266750
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The potent vasoconstrictor peptide, endothelin-1 (ET-1), which exhibits a characteristically long-acting activity in vitro and in vivo, is thought to be generated in endothelial cells from a less active intermediate, big endothelin-1 (big ET-1). In addition to ET-1, big ET-1 is also present in the circulation. The autoradiographic localization of I-125-big ET-1 and I-125-ET-1 has been studied after intravenous administration in rat tissues. Highest enrichment of radioactivity was found in the kidney cortex for both peptides. Compared to blood levels, enrichment of radioactivity is also detected, in the vascular wall of the aorta. Comparing the radioactivity pattern of ET-1 and big ET-1, a nearly identical tissue distribution is observed, with the exception of the relative enrichment in the lung and the zona glomerulosa after administration of ET-1. Both radioligands show a specific and saturable binding to lung and kidney membranes. In the case of lung tissue, K(i) values are 10(-10) M for endothelin-1 and 10(-8) M for big endothelin-1. This difference in affinities may account for the lack of binding of big endothelin-1 to lung tissue.
引用
收藏
页码:621 / 628
页数:8
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