Suppr超能文献

人隐静脉移植物中内皮素受体的表达与药理学

Endothelin receptor expression and pharmacology in human saphenous vein graft.

作者信息

Maguire J J, Davenport A P

机构信息

Clinical Pharmacology Unit, University of Cambridge, Level 6, Centre for Clinical Investigation, Addenbrooke's Hospital, England.

出版信息

Br J Pharmacol. 1999 Jan;126(2):443-50. doi: 10.1038/sj.bjp.0702326.

Abstract
  1. We have investigated the expression and pharmacology of endothelin (ET) receptors in human aortocoronary saphenous vein grafts. 2. Subtype-selective ligands were used to autoradiographically identify ET(A) ([125I]-PD151242) and ET(B)([125I]-BQ3020) receptors. In graft saphenous vein ETA receptors predominated in the media, with few ET(B) receptors identified. Neither subtype was detected in the thickened neointima. 3. The ratio of medial ET(A):ET(B) receptors was 75%: 25% in both graft and control saphenous vein. 4. ET-1 contracted control (EC50 2.9 nM) and graft (EC50 4.5 nM) saphenous vein more potently than diseased coronary artery (EC50 25.5 nM). 5. In all three blood vessels ET-1 was 100 times more potent than ET-3 and three times more potent than sarafotoxin 6b (S6b). Little or no response was obtained in any vessel with the ET(B) agonist sarafotoxin 6c (S6c). 6. The ET(A) antagonist PD156707 (100 nM) blocked ET-1 responses in all three vessels with pKb values of approximately 8.0. 7. For individual graft veins the EC50 value for ET-1 and 'age' of graft in years showed a significant negative correlation. 8. In conclusion there is no alteration in ET receptor expression in the media of saphenous veins grafted into the coronary circulation compared to control veins. ETA receptors predominantly mediate the vasoconstrictor response to ET-1 in graft vein, with no apparent up-regulation of ET(B) receptors. The sensitivity of the graft vein to ET-1 increased with graft 'age', suggesting that these vessels may be particularly vulnerable to the increased plasma ET levels that are detected in patients with cardiovascular disease.
摘要
  1. 我们研究了人主动脉冠状动脉大隐静脉移植物中内皮素(ET)受体的表达及药理学特性。2. 采用亚型选择性配体通过放射自显影法鉴定ET(A)([125I]-PD151242)和ET(B)([125I]-BQ3020)受体。在移植物大隐静脉中,ET(A)受体在中膜占主导,仅发现少量ET(B)受体。在增厚的新生内膜中未检测到任何一种亚型受体。3. 移植物和对照大隐静脉中膜ET(A):ET(B)受体的比例均为75%:25%。4. ET-1对对照大隐静脉(EC50 2.9 nM)和移植物大隐静脉(EC50 4.5 nM)的收缩作用比对病变冠状动脉(EC50 25.5 nM)更强。5. 在所有三种血管中,ET-1的效力比ET-3强100倍,比铃蟾毒素6b(S6b)强3倍。ET(B)激动剂铃蟾毒素6c(S6c)在任何血管中均未引起明显反应。6. ET(A)拮抗剂PD156707(100 nM)阻断了所有三种血管中ET-1的反应,pKb值约为8.0。7. 对于单个移植物静脉,ET-1的EC50值与移植物的“年龄”(以年计)呈显著负相关。8. 总之,与对照静脉相比,移植到冠状动脉循环中的大隐静脉中膜ET受体表达无改变。ET(A)受体主要介导移植物静脉对ET-1的血管收缩反应,ET(B)受体无明显上调。移植物静脉对ET-1的敏感性随移植物“年龄”增加,提示这些血管可能对心血管疾病患者中检测到的血浆ET水平升高特别敏感。

相似文献

6
Endothelin receptors in human coronary artery and aorta.人类冠状动脉和主动脉中的内皮素受体
Br J Pharmacol. 1996 Mar;117(5):986-92. doi: 10.1111/j.1476-5381.1996.tb15292.x.
7
ETA receptor antagonists inhibit intimal smooth muscle cell proliferation in human vessels.
Clin Sci (Lond). 2002 Aug;103 Suppl 48:184S-188S. doi: 10.1042/CS103S184S.

引用本文的文献

3
Endothelin.内皮素
Pharmacol Rev. 2016 Apr;68(2):357-418. doi: 10.1124/pr.115.011833.

本文引用的文献

1
PD156707: a potent antagonist of endothelin-1 in human diseased coronary arteries and vein grafts.
J Cardiovasc Pharmacol. 1998;31 Suppl 1:S239-40. doi: 10.1097/00005344-199800001-00067.
5
Increased endothelin ET(A) receptor expression in rat carotid arteries after balloon injury.
Peptides. 1997;18(2):247-55. doi: 10.1016/s0196-9781(96)00285-9.
7
Plasma endothelin-1 levels in adult patients undergoing coronary revascularization.
Cardiovasc Surg. 1996 Dec;4(6):808-12. doi: 10.1016/s0967-2109(96)00036-1.
8
In situ endothelin in coronary artery disease.冠状动脉疾病中的原位内皮素
Angiology. 1996 Nov;47(11):1027-32. doi: 10.1177/000331979604701101.
9
Endothelin-1 expression in vein graft stenosis.内皮素-1在静脉移植物狭窄中的表达。
J Vasc Surg. 1996 Nov;24(5):901-2. doi: 10.1016/s0741-5214(96)70030-7.
10
Endothelin peptide and receptors in human atherosclerotic coronary artery and aorta.
Circ Res. 1996 Oct;79(4):794-801. doi: 10.1161/01.res.79.4.794.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验