Debas H T
Fed Proc. 1977 Jun;36(7):1933-7.
The advent of the H2-histamine-receptor antagonists has given new life to the old hypothesis that histamine might be the final common chemical mediator of acid secretion. The available evidence, however, does not prove this hypothesis but does confer on histamine a role in the regulation of acid secretion in normal physiology. Evidence is mounting that, in addition to its stimulatory action, the vagus may play an inhibitory role in acid secretion and gastrin release. Our concepts of the gastric phase of acid secretion have been extended by the discovery of cross distension reflexes in the stomach: the pyloro-oxyntic reflex for acid secretion and the oxyntopyloric reflex for gastrin release. In addition, digested protein has been shown to stimulate directly the oxyntic gland mucosa, but the evidence is against a role for this mechanism in the intact stomach. The hormone(s) responsible for the intestinal phase have not been isolated but the physiological characteristics of entero-oxyntin (a nongastrin, enteric substance that acts on the oxyntic cell) have been defined. Gastric inhibitory polypeptide is an excellent candidate for the entero-gastrone released by fat, but whether it is the sole enterogastrone released is yet to be determined.
H2组胺受体拮抗剂的出现,为组胺可能是胃酸分泌的最终共同化学介质这一旧假说赋予了新的活力。然而,现有证据并未证实这一假说,但确实赋予了组胺在正常生理状态下胃酸分泌调节中的作用。越来越多的证据表明,迷走神经除了具有刺激作用外,可能在胃酸分泌和胃泌素释放中发挥抑制作用。胃内交叉扩张反射的发现扩展了我们对胃酸分泌胃期的认识:即促进胃酸分泌的幽门-泌酸反射和促进胃泌素释放的泌酸-幽门反射。此外,已证实消化后的蛋白质可直接刺激泌酸腺黏膜,但有证据表明该机制在完整胃中不起作用。负责肠期的激素尚未分离出来,但已明确了肠泌酸素(一种作用于泌酸细胞的非胃泌素肠道物质)的生理特性。胃抑制多肽是脂肪释放的肠抑胃素的极佳候选者,但它是否是唯一释放的肠抑胃素还有待确定。