Anteunis A, Gespach C, Astesano A, Emami S, Robineaux R, Rosselin G
Peptides. 1984 Mar-Apr;5(2):277-83. doi: 10.1016/0196-9781(84)90219-5.
We have studied the in vitro effect of VIP and histamine on ultrastructure of the parietal cells in isolated guinea pig fundic glands. The morphological changes induced by histamine in the parietal cells can be compared to those observed after histamine stimulation in vivo or in vitro on gastric mucosa preparations. In contrast, VIP incubation did not produce the ultrastructural changes related to gastric acid secretion, in resting parietal cells. Pretreatment of the glands by VIP resulted in a remarkable suppression of the histamine effect, since the parietal cells assumed an almost resting state. The data (1) indicate that the parietal cells in isolated gastric glands of the guinea pig retain in vitro the capacity to undergo the ultrastructural changes that are related to acid secretion in vivo after histamine or cAMP and (2) suggest that VIP is an inhibitor of histamine-induced gastric acid secretion in the guinea pig. It is proposed that VIP could act directly on the parietal cell via cAMP-phosphodiesterase activation, or indirectly via gastric somatostatin and/or prostaglandin secretions, inhibiting the H2 receptor-cAMP system of the parietal cell.
我们研究了血管活性肠肽(VIP)和组胺对豚鼠离体胃底腺壁细胞超微结构的体外作用。组胺诱导的壁细胞形态变化可与体内或体外组胺刺激胃黏膜制剂后观察到的变化相比较。相比之下,在静息壁细胞中,孵育VIP并未产生与胃酸分泌相关的超微结构变化。用VIP预处理腺体导致组胺效应显著受到抑制,因为壁细胞几乎处于静息状态。这些数据(1)表明,豚鼠离体胃腺中的壁细胞在体外保留了在组胺或环磷酸腺苷(cAMP)作用下发生与体内胃酸分泌相关的超微结构变化的能力,(2)提示VIP是豚鼠组胺诱导胃酸分泌的抑制剂。有人提出,VIP可能通过激活cAMP磷酸二酯酶直接作用于壁细胞,或通过胃生长抑素和/或前列腺素分泌间接作用,抑制壁细胞的H2受体-cAMP系统。