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乳酸受体HCAR1影响轴突发育,并在实验性新生儿低血糖中有助于乳酸对轴突和髓鞘的保护。

Lactate Receptor HCAR1 Affects Axonal Development and Contributes to Lactate's Protection of Axons and Myelin in Experimental Neonatal Hypoglycemia.

作者信息

Kennedy Lauritz, Morland Cecilie, Narum Martine, Bergersen Linda H, Rinholm Johanne E

机构信息

Department of Microbiology, Oslo University Hospital and University of Oslo, Oslo 0373, Norway.

Division of Physiology, Institute of Basic Medical Sciences, University of Oslo, Oslo 0372, Norway.

出版信息

eNeuro. 2025 May 30;12(5). doi: 10.1523/ENEURO.0563-24.2025. Print 2025 May.

Abstract

Lactate plays an important role in brain energy metabolism. It contributes to normal brain development and to neuroprotection in diabetic hypoglycemia, but its role in neonatal hypoglycemia is unclear. Moreover, lactate can work as a signaling substance via the lactate receptor HCAR1 (Hydroxycarboxylic acid receptor 1). Recent studies indicate that HCAR1 is protective in mouse models of neonatal hypoxic ischemia and has a role in metabolic regulation in glial cells during hypoglycemia. Here we have studied potential impacts of HCAR1 on axonal and myelin development in the cerebral cortex and corpus callosum of young (P21) wild-type (WT) mice and HCAR1 KO mice and in cortical organotypic brain slice cultures. The HCAR1 KO mice showed lower axonal area relative to WT in both cortex and corpus callosum. However, the myelin area was unaffected by HCAR1 KO. Using particle and colocalization analysis, we show that HCAR1 KO predominantly reduces axonal size in unmyelinated axons. Using an organotypic brain slice model of neonatal hypoglycemia, we find that lactate protects both axonal and myelin development in hypoglycemia, partially via HCAR1. Lastly, live imaging with a pH-sensitive dye on acute cortical brain slices indicates that cellular lactate uptake is influenced by HCAR1. In conclusion, our findings support a role of HCAR1 in axonal development and in lactate's protective effects in hypoglycemia.

摘要

乳酸在脑能量代谢中发挥着重要作用。它有助于正常的脑发育以及在糖尿病低血糖症中发挥神经保护作用,但其在新生儿低血糖症中的作用尚不清楚。此外,乳酸可通过乳酸受体HCAR1(羟基羧酸受体1)作为信号物质发挥作用。最近的研究表明,HCAR1在新生儿缺氧缺血小鼠模型中具有保护作用,并且在低血糖期间对神经胶质细胞的代谢调节起作用。在此,我们研究了HCAR1对幼年(P21)野生型(WT)小鼠和HCAR1基因敲除(KO)小鼠大脑皮质和胼胝体中轴突和髓鞘发育的潜在影响,以及在皮质器官型脑片培养中的影响。HCAR1基因敲除小鼠的皮质和胼胝体中的轴突面积相对于野生型小鼠较低。然而,髓鞘面积不受HCAR1基因敲除的影响。通过颗粒和共定位分析,我们表明HCAR1基因敲除主要减少了无髓鞘轴突的轴突大小。使用新生儿低血糖症的器官型脑片模型,我们发现乳酸在低血糖症中对轴突和髓鞘发育均有保护作用,部分是通过HCAR1实现的。最后,在急性皮质脑片上使用pH敏感染料进行实时成像表明,细胞对乳酸的摄取受HCAR1影响。总之,我们的研究结果支持HCAR1在轴突发育以及乳酸在低血糖症中的保护作用中发挥作用。

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