Hanssen L E, Hanssen K F, Myren J
Scand J Gastroenterol. 1977;12(4):391-4. doi: 10.3109/00365527709181678.
Five healthy students were investigated on two different days with or without a constant infusion of somatostatin (500 microgram/h) into an arm vein a fluoroscopically placed Lagerlöf tube was used for the collection of gastric and duodenal juice. After 30-min basal period, 40 ml 100 mmol/l HCl was infused into the midpart of the duodenum over 5 min through a thin catheter attached to the tube. Plasma immunoreactive secretin was measured by radioimmunoassay employing 125I-labelled synthetic secretin, antibody against synthetic secretin, and standards prepared from pure natural porcine secretin. Secretin levels without somatostatin infusion were 4.6+/-0.7 pmol/l (mean+/-S.E.M.) basally and rose to a peak of 21.8+/-6.2 pmol/l after duodenal acidification (p less than 0.05) and with somatostatin infusion were 4.4+/-0.4 pmol/l basally and rose to a peak of 6.7+/-1.7 pmol/l (n.s.) after duodenal acidification. Pancreatic bicarbonate output increased from 8.0+/-2.5 mumol/min (mean+/-S.E.M.) to 283+/-44 mumol/min without somatostatin infusion (p less than 0.05) and from 6.7+/-2.1 mumol/min to 70+/-13 mumol/min somatostatin (p less than 0.05). This study shows that somatostatin (500 microgram/h can inhibit the release of secretin and the pancreatic bicarbonate secretion after duodenal acidification in man.
选取五名健康学生,在两天内分别进行研究,研究过程中通过手臂静脉持续输注生长抑素(500微克/小时)或不输注,使用荧光透视放置的拉格洛夫管收集胃液和十二指肠液。在30分钟的基础期后,通过连接在该管上的细导管在5分钟内将40毫升100毫摩尔/升的盐酸注入十二指肠中部。采用放射免疫分析法测定血浆免疫反应性促胰液素,该方法使用125I标记的合成促胰液素、抗合成促胰液素抗体以及由纯天然猪促胰液素制备的标准品。不输注生长抑素时,促胰液素水平基础值为4.6±0.7皮摩尔/升(平均值±标准误),十二指肠酸化后升至峰值21.8±6.2皮摩尔/升(p<0.05);输注生长抑素时,促胰液素水平基础值为4.4±0.4皮摩尔/升,十二指肠酸化后升至峰值6.7±1.7皮摩尔/升(无统计学意义)。未输注生长抑素时,胰腺碳酸氢盐分泌量从8.0±2.5微摩尔/分钟(平均值±标准误)增加至283±44微摩尔/分钟(p<0.05);输注生长抑素时,胰腺碳酸氢盐分泌量从6.7±2.1微摩尔/分钟增加至70±13微摩尔/分钟(p<0.05)。本研究表明,生长抑素(500微克/小时)可抑制人体十二指肠酸化后促胰液素的释放及胰腺碳酸氢盐的分泌。