Augmentation of endothelial function by endothelin antagonism in human saphenous vein conduits

被引:11
作者
Dumont, AS
Lovren, F
McNeill, JH
Sutherland, GR
Triggle, CR
Anderson, TJ
Verma, S
机构
[1] Univ Virginia, Hlth Sci Ctr, Dept Neurol Surg, Charlottesville, VA 22908 USA
[2] Univ Calgary, Div Cardiol, Calgary, AB T2N 1N4, Canada
[3] Univ Calgary, Div Pharmacol & Therapeut, Calgary, AB T2N 1N4, Canada
[4] Univ Calgary, Div Neurosurg, Calgary, AB T2N 1N4, Canada
[5] Univ British Columbia, Div Pharmacol & Toxicol, Vancouver, BC, Canada
关键词
cerebral revascularization; endothelin; saphenous vein; bosentan;
D O I
10.3171/jns.2001.94.2.0281
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Object. Cerebral revascularization with saphenous vein (SV) conduits is used in the management of hard-to-treat lesions that require deliberate arterial occlusion and in selected patients with occlusive vascular disease. Endothelial dysfunction is thought to contribute to acute perioperative vasospasm and chronic graft atherosclerosis. In the present study the authors examined the contribution of the potent vasoconstrictor endothelin-1 (ET-1) to endothelial dysfunction in human SVs. Methods. The effects of an ETA,B receptor antagonist (bosentan). an ETA receptor antagonist (BQ-123), and an ETB receptor antagonist (BQ-788) on in vitro endothelium-dependent and -independent responses were studied in human SVs. Vascular segments were obtained in 34 patients who had undergone revascularization procedures, and isometric dose-response curves (DRCs) were constructed using the isolated tissue bath procedure as follows: 1) cumulative DRCs to norepinephrine; and 2) DRCs to acetylcholine (ACh) and sodium nitroprusside in the absence and presence of bosentan, BQ-123, or BQ-788. Maximal vasodilatory responses and sensitivity were compared between groups. In the presence of bosentan (Experiment 1) and BQ-123 or BQ-788 (Experiment 2), ACh responses were significantly augmented (percent maximum relaxation values: 7 +/- 2 [control] compared with 17 +/- 3 [bosen- tan], p < 0.002 [Experiment 1]; and 12 +/- 2 [control] compared with 29 +/- 2 [BQ-123] and 25 +/- 2 [BQ-788]. p < 0.003 and p < 0.002, respectively [Experiment 2]). The sensitivity of SVs to ACh was unaffected by treatment. These beneficial effects were specific for the endothelium. Conclusions. Blockade of ET receptors significantly improves endothelial function in SVs. Furthermore, these effects appear to be independently and maximally mediated by antagonism of either ETA or ETB receptors. Interventions aimed at improving endothelial function may serve to counter perioperative vasospasm and impede atherosclerosis in SVs used for revascularization procedures.
引用
收藏
页码:281 / 286
页数:6
相关论文
共 42 条
[1]   ENDOTHELIAL FUNCTION OF HUMAN GASTROEPIPLOIC ARTERY IN COMPARISON WITH SAPHENOUS-VEIN [J].
AKAR, F ;
UYDES, BS ;
AYRANCIOGLU, K ;
YENER, A ;
ASLAMACI, S ;
ARSAN, M ;
TORUNER, A ;
KANZIK, I .
CARDIOVASCULAR RESEARCH, 1994, 28 (04) :500-504
[2]   THERAPEUTIC EFFECTS OF ENDOTHELIN RECEPTOR ANTAGONISTS IN STROKE [J].
BARONE, FC ;
WILLETTE, RN ;
YUE, TL ;
FEURESTEIN, G .
NEUROLOGICAL RESEARCH, 1995, 17 (04) :259-264
[3]   CHANGES IN GRAFTS AND CORONARY-ARTERIES AFTER SAPHENOUS-VEIN AORTOCORONARY BYPASS-SURGERY - RESULTS AT REPEAT ANGIOGRAPHY [J].
BOURASSA, MG ;
CAMPEAU, L ;
LESPERANCE, J ;
GRONDIN, CM .
CIRCULATION, 1982, 65 (07) :90-97
[4]  
BOURASSA MG, 1984, AM J CARDIOL, V53, P102
[5]  
CLOZEL M, 1994, J PHARMACOL EXP THER, V270, P228
[6]  
COCKCROFT KM, 1999, PRINCIPLES NEUROSURG, P371
[7]   Reversed-flow saphenous vein grafts for cerebral revascularization - Technical note [J].
David, CA ;
Zabramski, JM ;
Spetzler, RF .
JOURNAL OF NEUROSURGERY, 1997, 87 (05) :795-797
[8]   NEW DEVELOPMENTS IN THE UNDERSTANDING OF CEREBRAL VASOREGULATION AND VASOSPASM - THE ENDOTHELIN NITRIC-OXIDE NETWORK [J].
EHRENREICH, H ;
SCHILLING, L .
CLEVELAND CLINIC JOURNAL OF MEDICINE, 1995, 62 (02) :105-116
[9]   The clinical potential of endothelin receptor antagonists in cardiovascular medicine [J].
Ferro, CJ ;
Webb, DJ .
DRUGS, 1996, 51 (01) :12-27
[10]  
GRONDIN CM, 1984, CIRCULATION S1, V70, P1208