Institute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland.
Nat Metab. 2020 Feb;2(2):179-191. doi: 10.1038/s42255-020-0170-4. Epub 2020 Feb 17.
It has been suggested that, in states of arousal, release of noradrenaline and β-adrenergic signalling affect long-term memory formation by stimulating astrocytic lactate production from glycogen. However, the temporal relationship between cortical activity and cellular lactate fluctuations upon changes in arousal remains to be fully established. Also, the role of β-adrenergic signalling and brain glycogen metabolism on neural lactate dynamics in vivo is still unknown. Here, we show that an arousal-induced increase in cortical activity triggers lactate release into the extracellular space, and this correlates with a fast and prominent lactate dip in astrocytes. The immediate drop in astrocytic lactate concentration and the parallel increase in extracellular lactate levels underline an activity-dependent lactate release from astrocytes. Moreover, when β-adrenergic signalling is blocked or the brain is depleted of glycogen, the arousal-evoked cellular lactate surges are significantly reduced. We provide in vivo evidence that cortical activation upon arousal triggers lactate release from astrocytes, a rise in intracellular lactate levels mediated by β-adrenergic signalling and the mobilization of lactate from glycogen stores.
有人提出,在觉醒状态下,去甲肾上腺素和β-肾上腺素能信号的释放通过刺激星形胶质细胞从糖原中产生乳酸来影响长期记忆的形成。然而,皮质活动与唤醒状态变化时细胞内乳酸波动之间的时间关系仍有待充分确定。此外,β-肾上腺素能信号转导和脑糖原代谢对体内神经乳酸动力学的作用尚不清楚。在这里,我们表明,皮质活动的唤醒诱导增加会触发乳酸释放到细胞外空间,并且这与星形胶质细胞中快速而显著的乳酸下降相关。星形胶质细胞中乳酸浓度的即时下降和细胞外乳酸水平的平行升高强调了星形胶质细胞中依赖于活性的乳酸释放。此外,当β-肾上腺素能信号转导被阻断或大脑中的糖原被耗尽时,唤醒引起的细胞内乳酸激增会明显减少。我们提供了体内证据表明,唤醒时的皮质激活会触发星形胶质细胞释放乳酸,β-肾上腺素能信号介导的细胞内乳酸水平升高以及从糖原库中动员乳酸。