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牛原代内皮细胞中内皮素与内皮舒张因子的相互作用:内皮素-3的选择性作用

Interactions of endothelins and EDRF in bovine native endothelial cells: selective effects of endothelin-3.

作者信息

Warner T D, Schmidt H H, Murad F

机构信息

Department of Pharmacology, Northwestern University Medical School, Chicago 60611.

出版信息

Am J Physiol. 1992 May;262(5 Pt 2):H1600-5. doi: 10.1152/ajpheart.1992.262.5.H1600.

DOI:10.1152/ajpheart.1992.262.5.H1600
PMID:1590465
Abstract

The tone of vascular smooth muscle is influenced by factors released from the endothelium, including endothelin (ET)-1 and endothelium-derived relaxing factor (EDRF). To better understand the interactions between these two mediators, we examined the release of both immunoreactive ET-1 (ir-ET-1) and EDRF from bovine aortic intact endothelium. Bovine aortas were opened longitudinally, washed, and clamped with the endothelium uppermost between two plates. The upper plate contained six openings forming identical and independent wells of endothelial cell monolayer. In experiments examining the release of EDRF, measured as accumulated NO2- and NO3- (NO chi -), we found that ET-3, calcium ionophore A23187 (A23187), acetylcholine (ACh), or ADP caused significant increase in NO chi- release, whereas ET-1 did not. These were significantly reduced in the presence of the EDRF/NO synthase inhibitor, NG-methyl-L-arginine (L-NMA). In a parallel series of experiments measuring EDRF release by stimulation of guanosine 3',5'-cyclic monophosphate (cGMP) accumulation in rat fetal lung (RFL)-6 cells, ET-3 but not ET-1 was also found to be active as a releaser of EDRF. A23187 caused an increase of ir-ET-1 release, whereas ACh, ADP, or the NO-containing compound sodium nitroprusside decreased the release of ir-ET-1. The depression in ir-ET-1 release in the presence of ACh or ADP was not seen when the endothelium was treated with L-NMA. When the cells were pretreated with 8-bromoguanosine 3',5'-cyclic monophosphate (8-bromo-cGMP), the release of ir-ET-1 in response to A23187 was significantly depressed.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

血管平滑肌的张力受内皮释放的多种因素影响,包括内皮素(ET)-1和内皮源性舒张因子(EDRF)。为了更好地理解这两种介质之间的相互作用,我们检测了牛主动脉完整内皮中免疫反应性ET-1(ir-ET-1)和EDRF的释放。将牛主动脉纵向切开,冲洗后,内皮面朝上夹在两块板之间。上板有六个开口,形成相同且独立的内皮细胞单层孔。在检测EDRF释放的实验中(以积累的NO2-和NO3-(NOχ-)衡量),我们发现ET-3、钙离子载体A23187(A23187)、乙酰胆碱(ACh)或ADP可显著增加NOχ-的释放,而ET-1则无此作用。在EDRF/一氧化氮合酶抑制剂NG-甲基-L-精氨酸(L-NMA)存在时,这些作用显著减弱。在一系列平行实验中,通过刺激大鼠胎肺(RFL)-6细胞中鸟苷3',5'-环磷酸(cGMP)积累来检测EDRF释放,结果发现ET-3而非ET-1也可作为EDRF的释放剂发挥作用。A23187可增加ir-ET-1的释放,而ACh、ADP或含NO的化合物硝普钠可降低ir-ET-1的释放。当用L-NMA处理内皮时,未观察到ACh或ADP存在时ir-ET-1释放的降低。当细胞用8-溴鸟苷3',5'-环磷酸(8-溴-cGMP)预处理后,A23187诱导的ir-ET-1释放显著降低。(摘要截短于250词)

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Evidence for the presence of endothelin ETA receptors in endothelial cells in situ on the aortic side of porcine aortic valve.
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