Carles-Bonnet C, Martinez J, Jarrousse C, Aumelas A, Niel H, Bataille D
INSERM U 376, CHU Arnaud-de-Villeneuve, Montpellier, France.
Peptides. 1996;17(3):557-61. doi: 10.1016/0196-9781(96)00001-0.
Oxyntomodulin inhibits gastric acid secretion via its C-terminal octapeptide. Its minimal active structure was delineated by testing, on histamine-stimulated gastric acid secretion in the conscious rat, the inhibitory effect of octapeptide analogues, shortened either or both on their N- or C- terminus. The octapeptide may be simplified by deleting the two C-terminal amino acids while keeping its efficacy and the slope of the dose-response curve. Suppressing the first N-terminal amino acid dramatically decreased the activity. The nonprotected peptides are metabolized by aminopeptidases and endopeptidases. The increased potency of the N-acetylated forms is related, at least in part, with their protection against aminopeptidases.
胃泌酸调节素通过其C端八肽抑制胃酸分泌。通过在清醒大鼠中测试八肽类似物对组胺刺激的胃酸分泌的抑制作用来确定其最小活性结构,这些类似物在其N端或C端或两端都被缩短。通过删除两个C端氨基酸同时保持其效力和剂量反应曲线的斜率,可以简化八肽。抑制第一个N端氨基酸会显著降低活性。未受保护的肽会被氨肽酶和内肽酶代谢。N-乙酰化形式效力的提高至少部分与其对氨肽酶的保护作用有关。