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二甲双胍加速培养的原代小脑颗粒神经元中的糖酵解乳酸生成。

Metformin Accelerates Glycolytic Lactate Production in Cultured Primary Cerebellar Granule Neurons.

作者信息

Blumrich Eva-Maria, Dringen Ralf

机构信息

Centre for Biomolecular Interactions Bremen, Faculty 2 (Biology/Chemistry), University of Bremen, P.O. Box 330440, 28334, Bremen, Germany.

Centre for Environmental Research and Sustainable Technology, University of Bremen, Bremen, Germany.

出版信息

Neurochem Res. 2019 Jan;44(1):188-199. doi: 10.1007/s11064-017-2346-1. Epub 2017 Jul 7.

Abstract

Metformin is the most frequently used drug for the treatment of type-II diabetes. As metformin has been reported to cross the blood-brain barrier, brain cells will encounter this drug. To test whether metformin may affect the metabolism of neurons, we exposed cultured rat cerebellar granule neurons to metformin. Treatment with metformin caused a time- and concentration-dependent increase in glycolytic lactate release from viable neurons as demonstrated by the three-to fivefold increase in extracellular lactate concentration determined after exposure to metformin. Half-maximal stimulation of lactate production was found after incubation of neurons for 4 h with around 2 mM or for 24 h with around 0.5 mM metformin. Neuronal cell viability was not affected by millimolar concentrations of metformin during acute incubations in the hour range nor during prolonged incubations, although alterations in cell morphology were observed during treatment with 10 mM metformin for days. The acute stimulation of neuronal lactate release by metformin was persistent upon removal of metformin from the medium and was not affected by the presence of modulators of adenosine monophosphate activated kinase activity. In contrast, rabeprazole, an inhibitor of the organic cation transporter 3, completely prevented metformin-mediated stimulation of neuronal lactate production. In summary, the data presented identify metformin as a potent stimulator of glycolytic lactate production in viable cultured neurons and suggest that organic cation transporter 3 mediates the uptake of metformin into neurons.

摘要

二甲双胍是治疗II型糖尿病最常用的药物。由于有报道称二甲双胍可穿过血脑屏障,脑细胞会接触到这种药物。为了测试二甲双胍是否会影响神经元的代谢,我们将培养的大鼠小脑颗粒神经元暴露于二甲双胍中。二甲双胍处理导致存活神经元糖酵解乳酸释放呈时间和浓度依赖性增加,这通过暴露于二甲双胍后测定的细胞外乳酸浓度增加三到五倍得以证明。在用约2 mM二甲双胍孵育神经元4小时或用约0.5 mM二甲双胍孵育24小时后,发现乳酸产生的半最大刺激。在急性孵育的一小时范围内以及长时间孵育期间,毫摩尔浓度的二甲双胍均未影响神经元细胞活力,尽管在用10 mM二甲双胍处理数天期间观察到细胞形态发生了改变。从培养基中去除二甲双胍后,二甲双胍对神经元乳酸释放的急性刺激持续存在,并且不受单磷酸腺苷激活激酶活性调节剂的影响。相比之下,有机阳离子转运体3的抑制剂雷贝拉唑完全阻止了二甲双胍介导的神经元乳酸产生的刺激。总之,所呈现的数据表明二甲双胍是存活培养神经元中糖酵解乳酸产生的有效刺激剂,并表明有机阳离子转运体3介导二甲双胍进入神经元的摄取。

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