Baum F, Nauck M A, Ebert R, Cantor P, Hoffmann G, Choudhury A R, Schmidt W E, Creutzfeldt W
Department of Medicine, Georg August University, Göttingen, FRG.
Digestion. 1992;53(3-4):189-99. doi: 10.1159/000200994.
To estimate the contribution of postprandial cholecystokinin (CCK) responses to circulating insulin concentrations and insulin secretion, a specific CCK receptor antagonist (loxiglumide; 10 mg/kg body weight/h) or saline were infused intravenously in normal volunteers, beginning 90 min before insulin secretion was stimulated on separate occasions by the intraduodenal administrations of glucose, glucose and protein, and glucose plus protein with the admixture of pancreatin. The release of CCK (radioimmunoassay) was stimulated by the protein component of the nutrients from basal 2.4 +/- 0.4 to 8.0 +/- 1.2 pmol/l. CCK plasma levels were significantly higher with loxiglumide (p < 0.05). Glucose-dependent insulinotropic polypeptide (GIP) was also released by all nutrient mixtures. Loxiglumide significantly inhibited the amount of bilirubin and pancreatic enzymes recovered from duodenal aspirates. In contrast, in none of the experiments, C-peptide increments and hence insulin secretion rates were altered by loxiglumide. With glucose and protein as intraduodenal stimulus (no pancreatin added), the plasma amino acids rose significantly less (by approximately 50% of the control experiment) and the increment in insulin (but not C-peptide) concentrations was significantly reduced by loxiglumide. This is most likely explained by a change in insulin metabolic clearance. This effect cannot be a primary action of CCK because there was no similar effect of loxiglumide with the same intraduodenal stimulus plus added pancreatin. Pancreatic enzymes reduced maldigestion secondary to loxiglumide effects on pancreatic exocrine secretion: The increment in circulating amino acid concentrations was similar with and without loxiglumide. In conclusion, CCK does not alter insulin secretion and, therefore, is not an incretin hormone in man. Blocking CCK actions on the exocrine pancreas by loxiglumide, however, can secondarily cause reductions in postprandial insulin profiles by altering insulin clearance. These changes are possibly related to reductions in circulating amino acid concentrations.
为评估餐后胆囊收缩素(CCK)反应对循环胰岛素浓度及胰岛素分泌的作用,在正常志愿者中,于不同时间通过十二指肠内给予葡萄糖、葡萄糖与蛋白质、葡萄糖加蛋白质并混合胰酶刺激胰岛素分泌前90分钟,静脉输注特异性CCK受体拮抗剂(洛谷酰胺;10毫克/千克体重/小时)或生理盐水。营养物质中的蛋白质成分可刺激CCK释放(放射免疫分析法),使其从基础水平的2.4±0.4皮摩尔/升升至8.0±1.2皮摩尔/升。使用洛谷酰胺时CCK血浆水平显著更高(p<0.05)。所有营养混合物均可释放葡萄糖依赖性促胰岛素多肽(GIP)。洛谷酰胺显著抑制从十二指肠抽吸物中回收的胆红素和胰腺酶量。相比之下,在所有实验中,洛谷酰胺均未改变C肽增量及胰岛素分泌率。以葡萄糖和蛋白质作为十二指肠内刺激物(未添加胰酶)时,血浆氨基酸升高显著减少(约为对照实验的50%),洛谷酰胺显著降低胰岛素(而非C肽)浓度的增量。这很可能是由胰岛素代谢清除率的变化所致。这种作用并非CCK的主要作用,因为在相同十二指肠内刺激物并添加胰酶的情况下,洛谷酰胺并无类似作用。胰腺酶减少了因洛谷酰胺对胰腺外分泌的影响而导致的消化不良:无论有无洛谷酰胺,循环氨基酸浓度的增量相似。总之,CCK不会改变胰岛素分泌,因此在人类中不是一种肠促胰岛素激素。然而,通过洛谷酰胺阻断CCK对外分泌胰腺的作用,可通过改变胰岛素清除率继而导致餐后胰岛素水平降低。这些变化可能与循环氨基酸浓度降低有关。