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细胞松弛素对分离的大鼠胃壁细胞功能的抑制作用。

Cytochalasin inhibition of isolated rat gastric parietal cell function.

作者信息

Rosenfeld G C, McAllister E, Thompson W J

出版信息

J Cell Physiol. 1981 Oct;109(1):53-7. doi: 10.1002/jcp.1041090107.

Abstract

Submicrogram concentrations (0.04-0.29 microM) of the microfilament disrupting agents cytochalasins D, E, and B (CD, CE, CB) were shown to inhibit secretagogue-stimulated 14C-aminopyrine accumulation (AP) in isolated rat gastric mucosal parietal cells. The microtubule disrupting agent colchicine had little influence on AP accumulation. Histamine- and dibutyryl cyclic AMP (DbcAMP)-stimulated AP accumulation was inhibited with an order of potency CD greater than CE approximately equal to CB. CB inhibition of these secretagogue actions was, however, only approximately 65-70% of the maximal stimulated response, whereas CD and CE caused 100% inhibition. On the other hand, carbamylcholine-stimulated AP accumulation was inhibited 100% by all cytochalasins tested with an order of potency CD approximately equal to CE greater than CB. These data are discussed in relation to acid secretagogue-induced morphological changes involving actin filament organization in parietal cells.

摘要

已表明,微丝破坏剂细胞松弛素D、E和B(CD、CE、CB)的亚微克浓度(0.04 - 0.29微摩尔)可抑制分离的大鼠胃黏膜壁细胞中促分泌剂刺激的14C - 氨基比林积累(AP)。微管破坏剂秋水仙碱对AP积累影响很小。组胺和二丁酰环磷腺苷(DbcAMP)刺激的AP积累受到抑制,其效力顺序为CD大于CE约等于CB。然而,CB对这些促分泌剂作用的抑制仅约为最大刺激反应的65 - 70%,而CD和CE则导致100%的抑制。另一方面,所有测试的细胞松弛素对氨甲酰胆碱刺激的AP积累均有100%的抑制作用,其效力顺序为CD约等于CE大于CB。本文结合酸促分泌剂诱导的涉及壁细胞肌动蛋白丝组织的形态学变化对这些数据进行了讨论。

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