Panconesi A, Anselmi B, Curradi C, Perfetto F, Piluso A, Franchi G
Institute of Internal Medicine IV, University of Florence, Italy.
Headache. 1994 Apr;34(4):194-7. doi: 10.1111/j.1526-4610.1994.hed3404194.x.
The vasoconstrictor activity of sumatriptan and ergotamine were compared by injecting these drugs in the hand vein of migraine subjects. We used the "venotest method", which permits the evaluation of the venoconstrictor effect of small doses of drugs, acting locally in the hand vein. Sumatriptan injected at increasing doses in the hand vein provoked contraction only at high doses (500 micrograms): venoconstriction lasted 5-15 minutes and was similar in intensity and duration to that induced by 0.5-1 micrograms of 5-hydroxytryptamine (5-HT). Likewise, ergotamine induced contraction only at a dose of 50 micrograms: this venoconstrictor effect was long lasting (at least 1 hour). Ergotamine-induced hand vein contraction, almost completely inhibited by ketanserin, seems mediated at least in part by 5-HT2 receptors, like the one induced by 5-HT and sumatriptan, already observed in a previous study. Clinical doses of ergotamine (0.25 mg intramuscular) and of sumatriptan (6 mg subcutaneous) do not provoke hand vein contraction for at least 1 hour: this could be due to a low activity of these drugs on the 5-HT2 vein receptors or a technique that is unsuitable to detect the vasoconstrictor effect of drugs given by the systemic route. The long lasting venoconstrictor effect of ergotamine may be due to a slow dissociation from receptor sites. The short vasoconstriction induced by sumatriptan could account for the recurrence of headache in many sumatriptan-treated migraine subjects.
通过将舒马曲坦和麦角胺注射到偏头痛患者的手部静脉中,比较了它们的血管收缩活性。我们使用了“静脉测试法”,该方法可以评估小剂量药物在手静脉局部发挥作用时的静脉收缩效果。将舒马曲坦以递增剂量注射到手部静脉中,仅在高剂量(500微克)时才引起收缩:静脉收缩持续5 - 15分钟,其强度和持续时间与0.5 - 1微克5 - 羟色胺(5 - HT)诱导的相似。同样,麦角胺仅在50微克剂量时引起收缩:这种静脉收缩作用持续时间长(至少1小时)。麦角胺诱导的手部静脉收缩几乎完全被酮色林抑制,这似乎至少部分是由5 - HT2受体介导的,就像之前研究中观察到的5 - HT和舒马曲坦诱导的收缩一样。临床剂量的麦角胺(0.25毫克肌肉注射)和舒马曲坦(6毫克皮下注射)至少1小时内不会引起手部静脉收缩:这可能是由于这些药物对5 - HT2静脉受体的活性较低,或者是由于该技术不适用于检测全身给药药物的血管收缩作用。麦角胺持久的静脉收缩作用可能是由于其从受体部位缓慢解离所致。舒马曲坦引起的短暂血管收缩可能解释了许多接受舒马曲坦治疗的偏头痛患者头痛复发的原因。