Gustavsson S, Johansson H, Lundqvist G, Nilsson F
Scand J Gastroenterol. 1977;12(8):993-7. doi: 10.3109/00365527709181363.
Vasoactive intestinal peptide (VIP) and the newly discovered pancreatic polypeptide (PP), both having been proposed as pathogenetic factors in the watery diarrhea syndrome (WDRA), were intravenously infused into rats in order to study the effect on small bowel propulsion. Simultaneously with the infusion of hormone, radioactive test substance was continuously infused into the duodenum of the conscious animal through a permanent catheter. By recording the distribution of radioactivity along the excised gastrointestinal tract, analyses of small bowel propulsion were possible. After infusion of VIP small bowel transit time was significantly prolonged, and the local propagation velocity was retarded both in the proximal and the distal part of the small bowel. PP did not alter small bowel populations. The heavily retarded transport rate after VIP is a propulsive dysfunction and not inconsistent with the clinical sign of diarrhea.
血管活性肠肽(VIP)和新发现的胰多肽(PP)都被认为是水样腹泻综合征(WDRA)的致病因素,为了研究它们对小肠推进的影响,将其静脉注射到大鼠体内。在注入激素的同时,放射性测试物质通过一根永久性导管持续注入清醒动物的十二指肠。通过记录沿切除的胃肠道的放射性分布,就可以对小肠推进进行分析。注入VIP后,小肠通过时间显著延长,小肠近端和远端的局部传播速度均减慢。PP没有改变小肠推进情况。VIP注入后运输速率严重减慢是一种推进功能障碍,与腹泻的临床症状相符。