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Glucose and lactate metabolism in the awake and stimulated rat: a 13C-NMR study

机译:清醒和刺激的大鼠中的葡萄糖和乳酸代谢:13C-NMR研究

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摘要

Glucose is the major energetic substrate for the brain but evidence has accumulated during the last 20 years that lactate produced by astrocytes could be an additional substrate for neurons. However, little information exists about this lactate shuttle in vivo in activated and awake animals. We designed an experiment in which the cortical barrel field (S1BF) was unilaterally activated during infusion of both glucose and lactate (alternatively labeled with 13C) in rats. At the end of stimulation (1 h) both S1BF areas were removed and analyzed by HR-MAS NMR spectroscopy to compare glucose and lactate metabolism in the activated area vs. the non-activated one. In combination with microwave irradiation HR-MAS spectroscopy is a powerful technical approach to study brain lactate metabolism in vivo. Using in vivo 14C-2-deoxyglucose and autoradiography we confirmed that whisker stimulation was effective since we observed a 40% increase in glucose uptake in the activated S1BF area compared to the ipsilateral one. We first determined that lactate observed on spectra of biopsies did not arise from post-mortem metabolism. 1H-NMR data indicated that during brain activation there was an average 2.4-fold increase in lactate content in the activated area. When [1-13C]glucose + lactate were infused 13C-NMR data showed an increase in 13C-labeled lactate during brain activation as well as an increase in lactate C3-specific enrichment. This result demonstrates that the increase in lactate observed on 1H-NMR spectra originates from newly synthesized lactate from the labeled precursor ([1-13C]glucose). It also shows that this additional lactate does not arise from an increase in blood lactate uptake since it would otherwise be unlabeled. These results are in favor of intracerebral lactate production during brain activation in vivo which could be a supplementary fuel for neurons.
机译:葡萄糖是大脑的主要能量底物,但在过去的20年中,已有证据表明,星形胶质细胞产生的乳酸可能是神经元的另一种底物。但是,关于在活化和清醒的动物体内这种乳酸穿梭的信息很少。我们设计了一个实验,在大鼠输注葡萄糖和乳酸(或用 13 C标记)期间,单侧激活了皮质桶区(S1BF)。刺激结束后(1小时),两个S1BF区域均被移除并通过HR-MAS NMR光谱分析,以比较活化区域和非活化区域的葡萄糖和乳酸代谢。结合微波辐射,HR-MAS光谱技术是研究体内脑乳酸代谢的强大技术手段。使用体内 14 C-2-脱氧葡萄糖和放射自显影,我们确认了晶须刺激是有效的,因为我们观察到与同侧相比,活化的S1BF区域的葡萄糖摄取增加了40%。我们首先确定在活组织检查的光谱中观察到的乳酸不是由验尸后代谢产生的。 1 H-NMR数据表明,在大脑激活过程中,激活区域的乳酸含量平均增加了2.4倍。注入[1- 13 C]葡萄糖+乳酸盐时, 13 C-NMR数据显示脑激活过程中 13 C标记的乳酸增加以及乳酸C3特异性富集的增加。该结果表明,在 1 H-NMR光谱中观察到的乳酸的增加源自标记的前体([1- 13 C]葡萄糖)的新合成的乳酸。它还表明,这种额外的乳酸不是由于血液中乳酸摄取的增加而引起的,因为否则它就不会被标记。这些结果有利于体内脑激活期间脑内乳酸的产生,这可能是神经元的补充燃料。

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