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Relationship between intracellular pH and metabolite concentrations during metabolic inhibition in isolated ferret heart.

机译:离体雪貂心脏代谢抑制过程中细胞内pH与代谢物浓度之间的关系。

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摘要

1. Intracellular pH (pHi) and phosphorus metabolites were measured in isolated ferret hearts with 31P nuclear magnetic resonance (NMR). 2. The application of cyanide (to mimic hypoxia) produced a fall of the concentration of phosphocreatine ([PCr]) and a rise of those of inorganic phosphate ([Pi]) and sugar phosphates. These were accompanied by an intracellular acidosis. 3. If glycolysis was partly inhibited by prior exposure to a glucose-free solution then the application of cyanide also produced a fall of [ATP]. The acidosis was similar to that observed in the presence of glucose. 4. If glycolysis was completely inhibited by iodoacetate then the acidosis produced by subsequent addition of cyanide developed more quickly. 5. The results are reproduced by a model which incorporates lactic acid production as well as the effects of protons released and absorbed by the changes in metabolite concentrations. The results suggest that the acidosis produced by cyanide (without inhibition of glycolysis) is largely due to lactic acid production. When glycolysis is partly inhibited (glucose-free solution) the acidosis produced by cyanide is partly due to protons released by ATP breakdown. Finally, when glycolysis is entirely inhibited the acidosis is completely due to ATP breakdown. There is no need to postulate a contribution on this time scale from inhibition of pH regulating mechanisms.
机译:1.在孤立的雪貂心脏中通过31P核磁共振(NMR)测量细胞内pH(pHi)和磷代谢物。 2.施用氰化物(以模拟低氧)导致磷酸肌酸([PCr])浓度的下降以及无机磷酸酯(Pi)和糖磷酸酯的浓度的上升。这些伴有细胞内酸中毒。 3.如果事先暴露于无葡萄糖溶液中,部分地抑制了糖酵解作用,那么氰化物的施用也会使[ATP]下降。酸中毒类似于在葡萄糖存在下观察到的酸中毒。 4.如果糖酵解完全被碘乙酸盐抑制,那么随后添加氰化物产生的酸中毒发展得更快。 5.结果通过一个模型进行再现,该模型结合了乳酸的产生以及代谢物浓度变化释放和吸收的质子的影响。结果表明,氰化物产生的酸中毒(不抑制糖酵解作用)在很大程度上是由于乳酸的产生。当部分抑制糖酵解(无葡萄糖溶液)时,氰化物产生的酸中毒部分归因于ATP分解释放的质子。最后,当糖酵解被完全抑制时,酸中毒完全归因于ATP分解。无需在此时间范围内假设pH调节机制受到抑制。

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