Forearm vascular response to nitric oxide and calcitonin gene-related peptide: comparison between migraine patients and control subjects

被引:28
作者
de Hoon, JNJM
Smits, P
Troost, J
Struijker-Boudier, HAJ
Van Bortel, LMAB
机构
[1] Univ Hosp Gasthuisberg, Ctr Clin Pharmacol, B-3000 Louvain, Belgium
[2] Maastricht Univ, Dept Pharmacol & Toxicol, Inst Cardiovasc Res, Maastricht, Netherlands
[3] Univ Nijmegen, Div Gen Internal Med, Dept Med, Nijmegen, Netherlands
[4] Univ Nijmegen, Div Gen Internal Med, Dept Pharmacol & Toxicol, Nijmegen, Netherlands
[5] Univ Hosp Maastricht, Dept Neurol, Maastricht, Netherlands
[6] State Univ Ghent, Heymans Inst Pharmacol, B-9000 Ghent, Belgium
关键词
CGRP; endothelium; migraine; nitric oxide; vascular responsiveness;
D O I
10.1111/j.1468-2982.2005.00993.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The forearm vascular response to nitric oxide (NO) and calcitonin gene-related peptide (CGRP) was investigated in 10 migraine patients and 10 matched control subjects. Changes in forearm blood flow (FBF) during intrabrachial infusion of: (i) serotonin (releasing endogenous NO), (ii) sodium nitroprusside (SNP, exogenous NO-donor), and (iii) CGRP were measured using venous occlusion plethysmography. Flow-mediated dilation (FMD) of the brachial artery, a measure for the endogenous release of NO reactive to occlusion, was measured using ultrasound and expressed as percentage change vs. baseline diameter. FBF ratio (i.e. FBF in the infused over the control arm) at baseline (1.1 +/- 0.1) did not differ between both populations. Serotonin, SNP and CGRP induced a dose-dependent increase (P < 0.001) in FBF ratio in controls (to 2.8 +/- 0.3, 6.7 +/- 1.4 and 6.9 +/- 1.2 at the highest dose, respectively) and migraineurs (2.5 +/- 0.4, 5.6 +/- 0.8 and 6.5 +/- 1.3, respectively); these ratios did not differ between both groups. FMD was comparable in control subjects (5.8 +/- 1%) and migraine patients (5.2 +/- 1%). Based on the forearm vascular response to NO and CGRP, migraine patients do not display generalized changes in vascular function.
引用
收藏
页码:56 / 63
页数:8
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