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体内缺氧对大鼠脑突触体乙酰胆碱合成的影响。

Effects of in vivo hypoxia on acetylcholine synthesis by rat brain synaptosomes.

作者信息

Booth R F, Harvey S A, Clark J B

出版信息

J Neurochem. 1983 Jan;40(1):106-10. doi: 10.1111/j.1471-4159.1983.tb12659.x.

Abstract

Synaptosomes from normoxic and hypoxic rats were incubated aerobically in the presence and absence of veratridine. In the absence of veratridine, no significant difference was observed between the two types of preparation regarding either ATP/ADP ratio or 14CO2 or [14C]acetylcholine synthesis from D-[U-14C]glucose. However, in the presence of veratridine, significant reductions in the output of 14CO2 and [14C]acetylcholine by synaptosomes from hypoxic rats were apparent. It was concluded that irreversible metabolic lesions occur at the synapse as a result of hypoxia, which are apparent only when the metabolism of the preparation is accelerated to a level comparable with the maximal rate occurring in vivo. The presence of such lesions is further evidenced by the significant reductions in ATP/ADP ratio, 14CO2 output, and [14C]acetylcholine synthesis that occur in synaptosomes from hypoxic rats made anoxic in vitro and permitted to recover. Such decreases are not seen when synaptosomes from normoxic rats are similarly treated.

摘要

将常氧和低氧大鼠的突触体分别在有氧条件下、有无藜芦碱存在的情况下进行孵育。在没有藜芦碱的情况下,就ATP/ADP比值、14CO2或由D-[U-14C]葡萄糖合成[14C]乙酰胆碱而言,两种制剂之间未观察到显著差异。然而,在有藜芦碱存在的情况下,低氧大鼠突触体的14CO2和[14C]乙酰胆碱输出明显减少。得出的结论是,缺氧会导致突触处发生不可逆的代谢损伤,只有当制剂的代谢加速到与体内发生的最大速率相当的水平时,这种损伤才会明显显现。低氧大鼠的突触体在体外进行缺氧处理后再恢复,其ATP/ADP比值、14CO2输出和[14C]乙酰胆碱合成显著降低,进一步证明了这种损伤的存在。当常氧大鼠的突触体进行类似处理时,未观察到这种降低。

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