Pillay C V, Somers S, Booyens J, Moshal M G, Bryer J V
S Afr Med J. 1977 Jun 18;51(25):915-9.
The ultrastructure of the human parietal cell at rest, after stimulation of gastric acid secretion by pentagastrin and after inhibition with propantheline or cimetidine, an H2-receptor antagonist, was studied. On stimulation there was an increase in the total secretory surface area of the gastric gland and canaliculus, with a concomitant decrease in the tubulovesicular system. On inhibition there was a decrease in the secretory surface area and a corresponding increase in the tubulovesicular system. These results are in agreement with other reports and support the hypothesis that during secretion of acid the tubulovesicular system increases the secretory surface by eversion or fusion of the vesicles and tubules with the plasmalemma. On inhibition there is thought to be reformation of the tubulovesicular system by pinocytosis. There is also ultrastructural evidence for the theory of membrane flow between the tubulovesicular system and the microvilli of the canaliculus and gastric lumen. Furthermore, there was an increase in lysosomal activity after the administration of the inhibiting drugs. It is suggested that the increased lysosomal activity could be involved in reducing the quantity of membrane after the membrane flow which occurs on gastric acid inhibition.
研究了人壁细胞在静息状态下、经五肽胃泌素刺激胃酸分泌后以及用丙胺太林或西咪替丁(一种H2受体拮抗剂)抑制后的超微结构。刺激后,胃腺和小管的总分泌表面积增加,同时微管泡系统减少。抑制后,分泌表面积减少,微管泡系统相应增加。这些结果与其他报告一致,并支持这样的假说,即在胃酸分泌过程中,微管泡系统通过小泡和小管与质膜的外翻或融合增加分泌表面积。抑制时,认为通过胞饮作用重新形成微管泡系统。也有超微结构证据支持微管泡系统与小管和胃腔微绒毛之间的膜流理论。此外,给予抑制药物后溶酶体活性增加。提示溶酶体活性增加可能参与减少胃酸抑制时发生的膜流后膜的数量。