Kidder G W, Blankemeyer J T
Biochim Biophys Acta. 1978 Sep 11;512(1):192-8. doi: 10.1016/0005-2736(78)90229-8.
Using an improved spectrophotometer, we have reinvestigated the report (Hersey, S.J. (1974) Biochim. Biophys. Acta 344, 157--203) that acidification of the mucosal surface of frog gastric mucosa produces a crossover point between flavoprotein and cytochrome b, thus identifying a site of energy coupling between the cytochrome and H+ transport systems. While we find spectrophotometric changes upon addition of HCl to the mucosal solution, we find similar changes upon addition of NaCl without pH change, but no changes when the pH is lowered by substitution of H+ for Na+ at constant osmolality. We show that osmolality changes, with consequent alteration in tissue light scattering, are responsible for these effects. Further, we can show that the pH changes used do not inhibit acid secretion, and that one cannot do so without osmolality increase. We conclude that the imputed crossover point is not demonstrated, and that models based on its existence must be revised.
使用一台改进的分光光度计,我们重新研究了以下报告(赫西,S.J.(1974年)《生物化学与生物物理学学报》344卷,157 - 203页):青蛙胃黏膜表面酸化会在黄素蛋白和细胞色素b之间产生一个交叉点,从而确定了细胞色素与氢离子转运系统之间的能量偶联位点。虽然我们发现向黏膜溶液中添加盐酸后有分光光度变化,但在添加氯化钠且pH不变时也发现了类似变化,而在等渗条件下用氢离子替代钠离子降低pH时却没有变化。我们表明,渗透压变化以及随之而来的组织光散射改变是造成这些效应的原因。此外,我们可以证明所使用的pH变化并不抑制胃酸分泌,而且不增加渗透压就无法做到这一点。我们得出结论,所谓的交叉点并未得到证实,基于其存在的模型必须修订。