Bunnett N W, Turner A J, Debas H T
Department of Surgery, University of California, San Francisco 94143.
Q J Exp Physiol. 1989 Sep;74(5):727-34. doi: 10.1113/expphysiol.1989.sp003324.
The purpose of this investigation was to examine the metabolism and inactivation of gastrin releasing peptide 10 (GRP10) by endopeptidase-24.11 prepared from the stomach wall. GRP10 was metabolized in vitro by gastric endopeptidase-24.11. The metabolites were purified by high-pressure liquid chromatography and identified as (1-8) GRP10 and (9-10) GRP10 by amino acid analysis, indicating hydrolysis of the His8-Leu9 bond. The intravenous administration of GRP10 to conscious dogs stimulated gastrin release, gastric acid secretion, pancreatic protein secretion and pancreatic bicarbonate secretion. Incubation of GRP10 with endopeptidase-24.11 significantly diminished the biological activity of the digests compared to control digests containing heat-inactivated enzyme. This effect was abolished by the enzyme inhibitor phosphoramidon. It is concluded that endopeptidase-24.11 from the stomach metabolizes and inactivates GRP10.
本研究的目的是检测从胃壁制备的内肽酶-24.11对胃泌素释放肽10(GRP10)的代谢及失活作用。GRP10在体外被胃内肽酶-24.11代谢。代谢产物通过高压液相色谱法纯化,并经氨基酸分析鉴定为(1-8)GRP10和(9-10)GRP10,表明His8-Leu9键发生了水解。给清醒犬静脉注射GRP10可刺激胃泌素释放、胃酸分泌、胰腺蛋白质分泌和胰腺碳酸氢盐分泌。与含有热失活酶的对照消化物相比,GRP10与内肽酶-24.11孵育显著降低了消化物的生物活性。酶抑制剂磷酰胺可消除这种作用。得出的结论是,来自胃的内肽酶-24.11可代谢并使GRP10失活。