Laboratory of Exercise Biochemistry and Neuroendocrinology, University of Tsukuba, Tsukuba 305-8574, Ibaraki, Japan.
Department of Sport Neuroscience, Advanced Research Initiative for Human High Performance (ARIHHP), Faculty of Health and Sport Sciences, University of Tsukuba, Tsukuba 305-8574, Ibaraki, Japan.
Proc Natl Acad Sci U S A. 2017 Jun 13;114(24):6358-6363. doi: 10.1073/pnas.1702739114. Epub 2017 May 17.
Brain glycogen stored in astrocytes provides lactate as an energy source to neurons through monocarboxylate transporters (MCTs) to maintain neuronal functions such as hippocampus-regulated memory formation. Although prolonged exhaustive exercise decreases brain glycogen, the role of this decrease and lactate transport in the exercising brain remains less clear. Because muscle glycogen fuels exercising muscles, we hypothesized that astrocytic glycogen plays an energetic role in the prolonged-exercising brain to maintain endurance capacity through lactate transport. To test this hypothesis, we used a rat model of exhaustive exercise and capillary electrophoresis-mass spectrometry-based metabolomics to observe comprehensive energetics of the brain (cortex and hippocampus) and muscle (plantaris). At exhaustion, muscle glycogen was depleted but brain glycogen was only decreased. The levels of MCT2, which takes up lactate in neurons, increased in the brain, as did muscle MCTs. Metabolomics revealed that brain, but not muscle, ATP was maintained with lactate and other glycogenolytic/glycolytic sources. Intracerebroventricular injection of the glycogen phosphorylase inhibitor 1,4-dideoxy-1,4-imino-d-arabinitol did not affect peripheral glycemic conditions but suppressed brain lactate production and decreased hippocampal ATP levels at exhaustion. An MCT2 inhibitor, α-cyano-4-hydroxy-cinnamate, triggered a similar response that resulted in lower endurance capacity. These findings provide direct evidence for the energetic role of astrocytic glycogen-derived lactate in the exhaustive-exercising brain, implicating the significance of brain glycogen level in endurance capacity. Glycogen-maintained ATP in the brain is a possible defense mechanism for neurons in the exhausted brain.
大脑中的星形胶质细胞储存糖原,通过单羧酸转运蛋白(MCTs)将其转化为乳酸,为神经元提供能量,以维持海马体调节的记忆形成等神经元功能。尽管长时间的剧烈运动可导致脑糖原减少,但这种减少和乳酸转运在运动大脑中的作用仍不明确。由于肌肉糖原为运动肌肉提供燃料,我们假设星形胶质细胞糖原在长时间运动的大脑中发挥能量作用,通过乳酸转运来维持耐力能力。为了验证这一假设,我们使用了一种力竭运动的大鼠模型,并结合毛细管电泳-质谱代谢组学,观察大脑(皮质和海马体)和肌肉(比目鱼肌)的综合能量学。在力竭时,肌肉糖原被耗尽,但脑糖原仅减少。神经元摄取乳酸的 MCT2 水平在大脑中增加,肌肉 MCTs 也增加。代谢组学显示,大脑而不是肌肉的 ATP 水平通过乳酸和其他糖异生/糖酵解来源得以维持。脑室注射糖原磷酸化酶抑制剂 1,4-二脱氧-1,4-亚氨基-D-阿拉伯糖醇(1,4-dideoxy-1,4-imino-D-arabinitol)不会影响外周血糖水平,但可抑制脑乳酸生成,并在力竭时降低海马体 ATP 水平。MCT2 抑制剂 α-氰基-4-羟基肉桂酸(α-cyano-4-hydroxy-cinnamate)引发了类似的反应,导致耐力能力下降。这些发现为星形胶质细胞糖原衍生的乳酸在剧烈运动大脑中的能量作用提供了直接证据,表明脑糖原水平对耐力能力具有重要意义。大脑中由糖原维持的 ATP 可能是耗竭大脑中神经元的一种防御机制。