Secretagogue-dependent and -independent transport of zinc hydration forms in rat parietal cells

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• 作者：Florentina Sophie Ferstl ; Alice Miriam Kitay…
• 关键词：Stomach ; Gastric acid secretion ; NKCC1 co ; transporter ; Bumetanide ; Newport green
• 刊名：Pflügers Archiv - European Journal of Physiology
• 出版年：2016
• 出版时间：November 2016
• 年：2016
• 卷：468
• 期：11-12
• 页码：1877-1883
• 全文大小：
• 刊物主题：Human Physiology; Molecular Medicine; Neurosciences; Cell Biology; Receptors;
• 出版者：Springer Berlin Heidelberg
• ISSN：1432-2013
• 卷排序：468

文摘

Prolonged exposure to gastric acid is a leading cause of gastroesophageal reflux disease (GERD) and esophagitis. With the ever increasing number of patients showing insensitivity to proton-pump-inhibitor (PPI) therapy with recurrence of symptoms over time, alternative treatment options remain an important issue. Previous studies from our laboratory have shown that a zinc sulfate salt can inhibit HCl generation at the cellular level of the parietal cell. In this paper, we examine the difference between two hydration forms of ZnSO₄ (monohydrate H₂O and heptahydrate 7H₂O) in their entry characteristics into the parietal cell under several physiological conditions associated with acid secretion. Using the Zn sensitive fluorochrome Newport Green, we examined the rate of Zn entry in Δfluorescent units/second (ΔFU/second), at two different concentrations for both hydration states on both fasted and non-fasted animals. In a separate series of studies, we examined the effects of secretagogues on the entry rates and transport mechanisms. Exposure of the secretagogue carbachol transformed the resting parietal cell to an activated state and represents a stimulated condition through the neuronal pathway. The hormonal activation of the parietal cell was achieved by using histamine. Non-fasted conditions were considered to be a state between hormonal and neuronal activation. To demonstrate that ZnSO₄ enters the parietal cell through the NKCC1 co-transporter, the inhibitor bumetanide was applied during secretagogue-stimulated acid secretion. Both salts, monohydrate and heptahydrate ZnSO₄, show a concentration-dependent cell entry under all conditions studied. During stimulated acid secretion, induced through either the neuronal or the hormonal pathway, heptahydrate ZnSO₄ enters the parietal cell significantly faster than monohydrate ZnSO₄, whereas monohydrate ZnSO₄ exhibits faster entry during resting conditions in fasted animals. At 30 μM following stimulation with histamine, heptahydrate ZnSO₄ enters the cell faster than monohydrate ZnSO₄ (ΔFU/second 30 μM _{ZnSO4*7H2O + histamine} = 1.782, ΔFU/second 30 μM _{ZnSO4*H2O+histamine} = 1.038, respectively). Three hundred micromolar, heptahydrate ZnSO₄ shows a faster entry into the cells (ΔFU/second _{ZnSO4*7H2O300μM + carbachol} = 4.02407) compared to monohydrate ZnSO₄ (ΔFU/second _{ZnSO4*H2O300μM + carbachol} = 3.225) following exposure to carbachol. The mechanism of entry of both salts was found to be predominantly via the basolateral NKCC1 transporter with the rate of zinc entry decreasing to minimal values (ΔFU/second = 0.275) after application of bumetanide during stimulated conditions.