Tack J, Coulie B, Wilmer A, Peeters T, Janssens J
Department of Internal Medicine, University Hospital Gasthuisberg, Leuven, Belgium.
Gut. 1998 Jan;42(1):36-41. doi: 10.1136/gut.42.1.36.
Pharmacological studies of the enteric nervous system have shown the presence of several subtypes of 5-hydroxytryptamine (5HT) receptor, which might be involved in control of the migrating motor complex.
To study the effect of sumatriptan, an agonist of enteric neuronal 5HT1p receptors, on interdigestive motility in man.
In 12 healthy subjects, interdigestive motility was recorded manometrically in the upper gastrointestinal tract. In seven subjects blood samples were drawn every 15 minutes for radioimmunoassay of motilin and somatostatin. After two phase 3s of the migrating motor complex, 6 mg of sumatriptan was administered subcutaneously. Recording continued until two more phase 3s had occurred.
Sumatriptan induced a premature phase 3 in the jejunum after a median of 10 (8) minutes. The duration of the migrating 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 motilin concentrations and the occurrence of plasma motilin peaks were not affected. 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 the induction of a gastric phase 3 by the motilin agonist erythromycin.
Administration of the 5HT1P receptor agonist sumatriptan induces a premature intestinal phase 3, suppresses gastric phase 3s, prevents induction of a gastric phase 3 by erythromycin, and reduces plasma somatostatin concentrations.
对肠神经系统的药理学研究表明,存在几种5-羟色胺(5HT)受体亚型,它们可能参与移行性运动复合波的控制。
研究肠道神经元5HT1p受体激动剂舒马曲坦对人体消化间期运动的影响。
对12名健康受试者,通过测压法记录上消化道的消化间期运动。7名受试者每隔15分钟采集血样,用于放射免疫法检测胃动素和生长抑素。在移行性运动复合波的两个第3相之后,皮下注射6毫克舒马曲坦。记录持续到又出现两个第3相。
舒马曲坦在中位数为10(8)分钟后诱发空肠提前出现第3相。移行性运动复合波周期的持续时间缩短,第2相时间减少。注射舒马曲坦后,血浆生长抑素浓度降低,胃第3相受到抑制,尽管胃动素中位数浓度和血浆胃动素峰值的出现未受影响。注射舒马曲坦前的移行性运动复合波第3相与胃动素峰值相关,而注射后则不相关。此外,舒马曲坦预处理可防止胃动素激动剂红霉素诱发胃第3相。
给予5HT1P受体激动剂舒马曲坦可诱发肠道提前出现第3相,抑制胃第3相,防止红霉素诱发胃第3相,并降低血浆生长抑素浓度。