TRYPANOSOMA-CRUZI INDUCES ENDOTHELIN RELEASE FROM ENDOTHELIAL-CELLS

被引:43
作者
WITTNER, M
CHRIST, GJ
HUANG, H
WEISS, LM
HATCHER, VB
MORRIS, SA
ORR, GA
BERMAN, JW
ZEBALLOS, GA
DOUGLAS, SA
TANOWITZ, HB
机构
[1] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT PATHOL,BRONX,NY 10461
[2] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT MED,BRONX,NY 10461
[3] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT BIOCHEM,BRONX,NY 10461
[4] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT MOLEC PHARMACOL,BRONX,NY 10461
[5] YESHIVA UNIV ALBERT EINSTEIN COLL MED,DEPT UROL,BRONX,NY 10461
[6] MONTEFIORE MED CTR,BRONX,NY 10467
[7] COLUMBIA UNIV,COLL PHYS & SURG,DEPT MED,NEW YORK,NY
[8] COLUMBIA UNIV,COLL PHYS & SURG,DEPT PHARMACOL,NEW YORK,NY
[9] NEW YORK MED COLL,DEPT PHYSIOL,VALHALLA,NY 10595
[10] SMITHKLINE BEECHAM PHARMACEUT,DEPT CARDIOVASC PHARMACOL,KING OF PRUSSIA,PA 19406
关键词
D O I
10.1093/infdis/171.2.493
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The potential role of endothelin-1 (ET-1) in the pathogenesis of focal microvascular spasm, previously implicated in the etiology of Chagas' cardiomyopathy, was investigated. There was an increase in ET-1 in the supernatants of Trypanosoma cruzi-infected human umbilical vein endothelial cells (HUVEC). Infection of HUVEC and vascular smooth muscle cells had no effect on the synthesis of transforming growth factor-beta, which induces ET-1 synthesis. Bioassay studies of isolated rat aortic rings revealed that the increases in ET-1 production were associated with augmented contractile responses, which were significantly attenuated by preincubation with the ET, receptor antagonist, BQ-123. When big ET was incubated with the parasite, there was no conversion of the precursor to the active hormone (ET-1), demonstrating that the parasite did not possess the necessary converting enzyme. These observations suggest the potential importance of ET-1 in the etiology of the microvascular spasm associated with Chagas' disease.
引用
收藏
页码:493 / 497
页数:5
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