Nitric oxide-induced headache in patients with chronic tension-type headache

被引:118
作者
Ashina, M [1 ]
Bendtsen, L [1 ]
Jensen, R [1 ]
Olesen, J [1 ]
机构
[1] Univ Copenhagen, Glostrup Hosp, Dept Neurol, DK-2600 Glostrup, Denmark
关键词
tension-type headache; nitric oxide; central sensitization; glyceryl trinitrate; primary headaches;
D O I
10.1093/brain/123.9.1830
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
An experimental model of headache offers unique possibilities to study the mechanisms responsible for head pain, Using the glyceryl trinitrate [GTN; nitric oxide (NO) donor] model of experimental headache, we studied the intensity, quality and time profile of headache after infusion of GTN in 16 patients with chronic tension-type headache and in 16 healthy controls. Subjects were randomized to receive intravenous infusion of GTN (0.5 mu g/kg per minute for 20 min) or placebo on two headache-free days separated by at least 1 week, Headache intensity was measured on a 10-point verbal rating scale during 2 h of observation and for the next 10 h after discharge from hospital, The primary endpoints were the difference between the area under the curve (AUC-intensities x duration) for headache recorded on the day of GTN treatment and on the day of placebo treatment in patients, and in patients and controls on the days of GTN treatment, In patients, the AUC on a GTN day [2221 (1572-3704); median with quartiles in parentheses], was significantly greater than on a placebo day [730 (60-1678), P = 0.008], On the GTN day, the AUC in patients [2221 (1572-3704)] was significantly higher than in controls [43 (0-972), P = 0.0001]. In patients, peak pain intensity occurred 8 h after infusion of GTN, whereas in controls it occurred 20 min after the start of infusion. The present study demonstrates that an NO-induced biphasic response with an immediate and a delayed headache is common to chronic tension-type headache and migraine. Furthermore, the NO-induced delayed headache has the characteristics of the primary headache disorder. This suggests that NO contributes to the mechanisms of several types of primary headaches and that NO-related central sensitization may be an important common denominator in the pain mechanisms of primary headaches.
引用
收藏
页码:1830 / 1837
页数:8
相关论文
共 32 条
[1]  
Aley KO, 1998, J NEUROSCI, V18, P7008
[2]   Effect of inhibition of nitric oxide synthase on chronic tension-type headache: a randomised crossover trial [J].
Ashina, M ;
Lassen, LH ;
Bendtsen, L ;
Jensen, R ;
Olesen, J .
LANCET, 1999, 353 (9149) :287-289
[3]   Qualitatively altered nociception in chronic myofascial pain [J].
Bendtsen, L ;
Jensen, R ;
Olesen, J .
PAIN, 1996, 65 (2-3) :259-264
[4]   INTRACELLULAR MESSENGERS CONTRIBUTING TO PERSISTENT NOCICEPTION AND HYPERALGESIA INDUCED BY L-GLUTAMATE AND SUBSTANCE-P IN THE RAT FORMALIN PAIN MODEL [J].
CODERRE, TJ ;
YASHPAL, K .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1994, 6 (08) :1328-1334
[5]   Dural vasodilation causes a sensitization of rat caudal trigeminal neurones in vivo that is blocked by a 5-HT1B/1D agonist [J].
Cumberbatch, MJ ;
Williamson, DJ ;
Mason, GS ;
Hill, RG ;
Hargreaves, RJ .
BRITISH JOURNAL OF PHARMACOLOGY, 1999, 126 (06) :1478-1486
[6]   Responsiveness of the trigeminovascular system to nitroglycerine in cluster headache patients [J].
Fanciullacci, M ;
Alessandri, M ;
Sicuteri, R ;
Marabini, S .
BRAIN, 1997, 120 :283-288
[7]   NITRIC-OXIDE SIGNALING IN THE CENTRAL-NERVOUS-SYSTEM [J].
GARTHWAITE, J ;
BOULTON, CL .
ANNUAL REVIEW OF PHYSIOLOGY, 1995, 57 :683-706
[8]   ELECTROPHYSIOLOGICAL EVIDENCE FOR A ROLE OF NITRIC-OXIDE IN PROLONGED CHEMICAL NOCICEPTION IN THE RAT [J].
HALEY, JE ;
DICKENSON, AH ;
SCHACHTER, M .
NEUROPHARMACOLOGY, 1992, 31 (03) :251-258
[9]   A RATING SCALE FOR DEPRESSION [J].
HAMILTON, M .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1960, 23 (01) :56-62
[10]   Treatment of a chronic allodynia-like response in spinally injured rats: Effects of systemically administered nitric oxide synthase inhibitors [J].
Hao, JX ;
Xu, XJ .
PAIN, 1996, 66 (2-3) :313-319