Rees W D, Leigh R J, Christofides N D, Bloom S R, Turnberg L A
Gastroenterology. 1982 Sep;83(3):575-80.
Fasting antral, duodenal, and jejunal motor activity and plasma motilin and pancreatic polypeptide were studied in 14 patients with systemic sclerosis, 6 and 9 without clinical evidence of small bowel involvement, and 8 healthy control subjects. Normal interdigestive motor activity was present in control subjects and patients without intestinal involvement. However, cyclic motor activity was absent in 3 of the patients with intestinal disease and the motility index per interdigestive cycle (or per 6-h recording period in those without cyclic activity) was significantly less in the antrum (181 +/- 103 mm2 compared with 760 +/- 86 and 1116 +/- 96 mm2 for patients without involvement and healthy control subjects, respectively), duodenum (153 +/- 101 mm2 compared with 1425 +2- 186 nd 1055 +/- 241 mm2), and jejunum (268 +/- 131 mm2 compared with 1166 +/- 97 and 1105 +/- 128 mm2). Metoclopramide and bethanechol significantly increased motor activity at the three sites in all subjects but the magnitude of the metoclopramide response was less in patients with intestinal involvement. Fasting concentrations of motilin and pancreatic polypeptide exhibited cyclic variation with peak values occurring during phase 3 of the interdigestive cycle. Plasma motilin during each phase of motor activity was significantly higher in patients with scleroderma, with or without intestinal involvement, than in control subjects. The abnormal motor activity demonstrated here indicates a possible mechanism by which intestinal stasis and bacterial overgrowth could occur and by which clinical disturbances of intestinal transit might arise.
对14例系统性硬化症患者、6例无小肠受累临床证据的患者、9例无小肠受累临床证据的患者以及8名健康对照者进行了空腹时胃窦、十二指肠和空肠的运动活性以及血浆胃动素和胰多肽的研究。健康对照者和无肠道受累的患者存在正常的消化间期运动活性。然而,3例肠道疾病患者不存在周期性运动活性,并且每个消化间期(或对于无周期性活性的患者,每6小时记录期)的运动指数在胃窦(分别为181±103mm²,无受累患者为760±86mm²,健康对照者为1116±96mm²)、十二指肠(分别为153±101mm²,无受累患者为1425±186mm²,健康对照者为1055±241mm²)和空肠(分别为268±131mm²,无受累患者为1166±97mm²,健康对照者为1105±128mm²)显著降低。甲氧氯普胺和氨甲酰甲胆碱可显著增加所有受试者三个部位的运动活性,但在肠道受累患者中,甲氧氯普胺反应的幅度较小。空腹时胃动素和胰多肽的浓度呈现周期性变化,峰值出现在消化间期的第3期。无论有无肠道受累,系统性硬化症患者运动活性各阶段的血浆胃动素均显著高于对照者。此处显示的异常运动活性表明了肠道淤滞和细菌过度生长可能发生的一种潜在机制,以及肠道转运临床紊乱可能出现的机制。