Kierska D, Sasiak K, Maśliński C
Agents Actions. 1978 Oct;8(5):470-3. doi: 10.1007/BF02111430.
We have studied the dynamics of cyclic compound formation between histamine or histidine and pyridoxal 5'-phosphate (Hi-PLP or His-PLP) in incubates of rat gastric mucosa histidine decarboxylase (HD), rat intestinal diamine oxidase (DAO) or homogenates of either rat liver, intestine or gastric mucosa. For gastric mucosa HD, liver and gastric mucosa homogenates, the rate of cyclization was slightly decreased; however, the rate was significantly inhibited with intestinal DAO or intestinal homogenate. Binding of PLP by tissue components was measured; free PLP was bound abundantly by rat intestinal DAO and by rat intestinal homogenate. A possible mechanism by which intestinal tissues inhibit cyclic compound formation is discussed.
我们研究了在大鼠胃黏膜组氨酸脱羧酶(HD)、大鼠肠二胺氧化酶(DAO)或大鼠肝脏、肠道或胃黏膜匀浆的孵育体系中,组胺或组氨酸与磷酸吡哆醛(Hi-PLP或His-PLP)之间环状化合物形成的动力学。对于胃黏膜HD、肝脏和胃黏膜匀浆,环化速率略有降低;然而,肠DAO或肠匀浆显著抑制了该速率。测定了组织成分与PLP的结合情况;游离PLP被大鼠肠DAO和大鼠肠匀浆大量结合。讨论了肠道组织抑制环状化合物形成的可能机制。