Enhanced endothelium-dependent vasodilator responses in patients with systemic vasculitis

被引:15
作者
Bruce, IN
Harris, CM
Nugent, A
McDermott, BJ
Johnston, GD
Bell, AL
机构
[1] ROYAL VICTORIA HOSP,BELFAST BT12 6BA,ANTRIM,NORTH IRELAND
[2] MUSGRAVE PK HOSP,DEPT RHEUMATOL,BELFAST,ANTRIM,NORTH IRELAND
[3] QUEENS UNIV BELFAST,SCH CLIN MED,PATHOGENESIS GRP,BELFAST,ANTRIM,NORTH IRELAND
[4] QUEENS UNIV BELFAST,SCH CLIN MED,DEPT THERAPEUT & PHARMACOL,BELFAST,ANTRIM,NORTH IRELAND
关键词
vasculitis; pathogenesis; nitric oxide;
D O I
10.1080/030097497199712063049
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The aim of the study was to investigate endothelium-dependent vasodilator responses in the forearm vasculature of patients with systemic vasculitis. We studied 10 patients with systemic vasculitis and 16 healthy control subjects using forearm venous occlusion plethysmography to assess changes in forearm blood how in response to acetylcholine (ACh). N-G-monomethyl-L-arginine (L-NMMA), was also used to assess the contribution of endothelium derived relaxing factor nitric oxide (EDRF/NO) to the vasodilator responses to acetylcholine. A significantly greater vasodilator response to ACh was seen in the patient group at all doses infused (p<0.01). After pre-infusion of L-NMMA the differences in ACh dilator responses were no longer significant. There was a greater magnitude of inhibition of ACh responses by L-NMMA , in the patient group. The enhanced vasodilator response to ACh observed was in part abolished by L-NMMA. suggesting that EDRF/NO is produced in excess in systemic vasculitis. The precise role Flayed by EDRF/NO in the pathogenesis of systemic vasculitis requires further study.
引用
收藏
页码:318 / 324
页数:7
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