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酸中毒诱导的突触体对高亲和力胆碱摄取的改变:pH值重新调整的影响

Acidosis-induced modifications of high-affinity choline uptake by synaptosomes: effects of pH readjustment.

作者信息

Cancela J M, Beley A

机构信息

Laboratoire de Pharmacodynamie, Faculté de Pharmacie, Dijon, France.

出版信息

Neurochem Res. 1995 Jul;20(7):863-7. doi: 10.1007/BF00969699.

Abstract

Acidosis (pH 6.0) led to significant decrease in high-affinity choline uptake by rat brain synaptosomes. The effects persisted following pH readjustment (7.4) of the incubation medium, consisting of decrease in both Km and Vmax of the affinity system. pH readjustment coincided with synaptosomal leakage of lactate dehydrogenase (LDH) and with instability of the synaptosomal suspension as evidenced from turbidity modifications of the preparation. LDH leakage occurred when acidosis was performed with lactic acid, whereas it was not seen following H3PO4 acidosis, probably because of the rapid diffusion of the protonated from of lactic acid across membranes. Turbidity modifications of the suspension were prevented by EDTA. The present results indicate that acidosis to pH level comparable to what is observed in brain ischemia is deleterious for cholinergic mechanisms. They also suggest that alkaline pH shifts that occur after blood reperfusion of ischemic brain tissue might be critical for the survival of cells.

摘要

酸中毒(pH 6.0)导致大鼠脑突触体对高亲和力胆碱的摄取显著减少。在将孵育培养基的pH值重新调整为(7.4)后,这种影响仍然存在,表现为亲和力系统的Km和Vmax均降低。pH值的重新调整与乳酸脱氢酶(LDH)从突触体中泄漏以及突触体悬浮液的不稳定性同时发生,这从制剂的浊度变化可以看出。当用乳酸进行酸中毒时会发生LDH泄漏,而在磷酸(H3PO4)酸中毒后则未观察到这种情况,这可能是因为乳酸的质子化形式能够快速跨膜扩散。悬浮液的浊度变化可通过乙二胺四乙酸(EDTA)来防止。目前的结果表明,与脑缺血时观察到的pH水平相当的酸中毒对胆碱能机制是有害的。它们还表明,缺血性脑组织血液再灌注后发生的碱性pH值变化可能对细胞存活至关重要。

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