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葡萄糖剥夺导致大鼠海马切片中腺苷的乳酸可预防增加和突触传递抑制。

Glucose deprivation results in a lactate preventable increase in adenosine and depression of synaptic transmission in rat hippocampal slices.

作者信息

Fowler J C

机构信息

Department of Physiology, Texas Tech Health Sciences Center, Lubbock 79430.

出版信息

J Neurochem. 1993 Feb;60(2):572-6. doi: 10.1111/j.1471-4159.1993.tb03187.x.

Abstract

The effect of glucose deprivation on adenosine levels and on synaptic transmission was investigated in rat hippocampal slices. Incubation of hippocampal slices either in glucose-free medium or in the presence of the glucose transport inhibitor cytochalasin B (50 microM) increased bath adenosine levels and depressed the extracellularly recorded synaptic potential or population spike. The addition of lactate (10 mM), a precursor for mitochondrial ATP generation, prevented the elevation in adenosine and the depression of the population spike. These results indicate that the neuroinhibitory modulator adenosine is elevated during glucose deprivation and contributes to the hypoglycemic depression of synaptic transmission. The increase in adenosine during glucose deprivation can be prevented by providing substrate for mitochondrial ATP generation. The present results indicate an interaction between lactate and adenosine such that an increase in lactate may contribute to a decline in adenosine production.

摘要

在大鼠海马切片中研究了葡萄糖剥夺对腺苷水平和突触传递的影响。将海马切片置于无葡萄糖培养基中或在葡萄糖转运抑制剂细胞松弛素B(50微摩尔)存在的情况下孵育,可提高孵育液中腺苷水平,并抑制细胞外记录的突触电位或群体峰电位。添加乳酸(10毫摩尔),一种线粒体ATP生成的前体,可防止腺苷升高和群体峰电位的抑制。这些结果表明,神经抑制调节剂腺苷在葡萄糖剥夺期间升高,并导致低血糖对突触传递的抑制作用。通过为线粒体ATP生成提供底物,可以防止葡萄糖剥夺期间腺苷的增加。目前的结果表明乳酸和腺苷之间存在相互作用,即乳酸增加可能有助于腺苷生成的减少。

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