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Omeprazole induces gastric transmucosal permeability to the peptide bradykinin

机译:奥美拉唑诱导胃黏膜通透性对缓激肽的影响

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摘要

AIM: To investigate omeprazole-induced transepithelial gastric leak and its effects on the permeability of the peptides bradykinin and oxytocin.METHODS: Rat gastric corpus tissue was isolated and mounted in an Ussing chamber apparatus to evaluate the permeability of 3H-bradykinin, 3H-oxytocin, and 14C-EDTA in the presence or absence of omeprazole. Thin-layer chromatography was performed to identify any metabolic breakdown products of the peptides resulting from permeation through the gastric tissue, and thereby calculate the true flux of the peptide.RESULTS: The flux rate of intact 3H-bradykinin increased substantially after omeprazole addition (109.5%) compared to the DMSO vehicle control (14%). No corresponding change in flux of intact 3H-oxytocin was observed under the same conditions (11.9% and 6.4% in the DMSO- and omeprazole-treated conditions, respectively). After exposure to omeprazole, the flux rate of 14C-EDTA also increased dramatically (122.3%) compared to the DMSO condition (36.3%).CONCLUSION: The omeprazole-induced gastric leak allows for transmucosal permeability to charged molecules as well as non-electrolytes. This induced leak will allow certain peptides to permeate.
机译:目的:探讨奥美拉唑引起的上皮胃漏及其对缓激肽和催产素肽通透性的影响。方法:分离大鼠胃体组织并置于Ussing室仪中,评价 3 H-缓激肽, 3 H-催产素和 14 C-EDTA。进行薄层色谱分析,鉴定出由于肽经胃组织渗透而引起的代谢分解产物,从而计算出该肽的真实通量。结果:完整的 3 H-通量与DMSO媒介物对照(14%)相比,加入奥美拉唑后缓激肽显着增加(109.5%)。在相同条件下(DMSO和奥美拉唑处理的条件分别为11.9%和6.4%),未观察到完整的 3 H-催产素通量的相应变化。暴露于奥美拉唑后,与DMSO条件(36.3%)相比, 14 C-EDTA的通量率也显着增加(122.3%)。结论:奥美拉唑引起的胃漏可使透粘膜通透性达到带电分子以及非电解质。这种诱导的泄漏将使某些肽渗透。

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