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Actions of the 5-hydroxytryptamine 1 receptor agonist sumatriptan on interdigestive gastrointestinal motility in man

机译:5-羟色胺1受体激动剂舒马曲坦的作用 消化系统胃肠动力的研究

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摘要

Background—Pharmacological studies of the entericnervous system have shown the presence of several subtypes of5-hydroxytryptamine (5HT) receptor, which might be involved incontrol of the migrating motor complex. 
Aims—To study the effect of sumatriptan, anagonist of enteric neuronal 5HT1P receptors, oninterdigestive motility in man. 
Subjects and methods—In 12 healthy subjects,interdigestive motility was recorded manometrically in the uppergastrointestinal tract. In seven subjects blood samples were drawnevery 15 minutes for radioimmunoassay of motilin and somatostatin.After two phase 3s of the migrating motor complex, 6 mg of sumatriptanwas administered subcutaneously. Recording continued until two morephase 3s had occurred. 
Results—Sumatriptan induced a premature phase 3 in the jejunum after a median of 10 (8) minutes. The duration of themigrating motor complex cycle was shortened at the expense of phase 2. After sumatriptan, plasma somatostatin concentrations were reduced and gastric phase 3s were suppressed, although median motilinconcentrations and the occurrence of plasma motilin peaks were notaffected. Phase 3s of the migrating motor complex preceding sumatriptan were associated with motilin peaks, while phase 3s after sumatriptan were not. Furthermore, pretreatment with sumatriptan prevented theinduction of a gastric phase 3 by the motilin agonist erythromycin. 
Conclusions—Administration of the5HT1P receptor agonist sumatriptan induces a prematureintestinal phase 3, suppresses gastric phase 3s, prevents induct-ion of a gastric phase 3 by erythromycin, and reduces plasmasomatostatin concentrations. 


机译:背景—肠神经系统的药理研究表明,存在5-羟基色胺(5HT)受体的几种亚型,这些亚型可能与迁移性运动复合体的控制有关。目的:研究舒马曲坦(肠神经元5HT1P受体激动剂)对人消化道蠕动的影响。受试者和方法-在12例健康受试者中,通过消化道上消化道记录了消化系统间的蠕动。在7名受试者中,每15分钟抽取一次血样进行胃动素和生长抑素的放射免疫分析。在迁移的运动复合物的两个3阶段后,皮下注射舒马普坦6 mg。记录继续进行,直到发生了另外两个阶段3。结果-中速10(8)分钟后,苏门曲普坦在空肠中诱导了3期过早。尽管不影响中位胃动素浓度和血浆胃动素峰值的发生,但以阶段2为代价缩短了迁移运动复合体周期的持续时间,但舒马曲坦治疗后血浆血浆生长抑素浓度降低,胃部3s抑制。舒马曲坦之前的迁移运动复合物的3s阶段与胃动素峰相关,而舒马曲坦之后的3s阶段与运动相关。此外,用舒马曲坦预处理可防止胃动素激动剂红霉素诱导胃相3的发生。结论—给予5HT1P受体激动剂舒马普坦可诱导肠道早熟阶段3,抑制胃癌阶段3s,防止红霉素诱导胃癌阶段3并降低血浆血浆他汀类药物的浓度。

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