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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Neurochemical changes in the developing rat hippocampus during prolonged hypoglycemia.
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Neurochemical changes in the developing rat hippocampus during prolonged hypoglycemia.

机译:长期低血糖期间发育中的大鼠海马中的神经化学变化。

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摘要

Hypoglycemia is common during development and is associated with the risk of neurodevelopmental deficits in human infants. The effects of hypoglycemia on the developing hippocampus are poorly understood. The sequential changes in energy substrates, amino acids and phosphocreatine were measured from the hippocampus during 180 min of insulin-induced hypoglycemia (blood glucose < 2.5 mmol/L) in 14-day-old rats using in vivo(1)H NMR spectroscopy. Hypoglycemia resulted in neuroglycopenia (brain glucose < 0.5 micromol/g). However, the phosphocreatine/creatine (PCr/Cr) ratio was maintained in the physiological range until approximately 150 min of hypoglycemia, indicating that energy supply was sufficient to meet the energy demands. Lactate concentration decreased soon after the onset of neuroglycopenia. Beyond 60 min, glutamine and glutamate became the major energy substrates. A precipitous decrease in the PCr/Cr ratio, indicative of impending energy failure occurred only after significant depletion of these amino acids. Once glutamate and glutamine were significantly exhausted, aspartate became the final energy source. N-acetylaspartate concentration remained unaltered, suggesting preservation of neuronal/mitochondrial integrity during hypoglycemia. Correction of hypoglycemia normalized the PCr/Cr ratio and partially restored the amino acids to pre-hypoglycemia levels. Compensatory neurochemical changes maintain energy homeostasis during prolonged hypoglycemia in the developing hippocampus.
机译:低血糖症在发育过程中很常见,并与人类婴儿神经发育缺陷的风险有关。低血糖对发育中的海马的影响知之甚少。使用体内(1)H NMR光谱法在14天大的大鼠胰岛素诱导的低血糖(血糖<2.5 mmol / L)180分钟期间从海马测量了能量底物,氨基酸和磷酸肌酸的顺序变化。低血糖会导致神经性血糖降低(脑葡萄糖<0.5 micromol / g)。然而,磷酸肌酸/肌酸(PCr / Cr)之比一直保持在生理范围内,直到低血糖约150分钟为止,这表明能量供应足以满足能量需求。神经糖减少症发作后不久,乳酸浓度下降。 60分钟后,谷氨酰胺和谷氨酸成为主要的能量底物。 PCr / Cr比值急剧下降,表明即将发生的能量衰竭仅在这些氨基酸大量消耗后才发生。一旦谷氨酸和谷氨酰胺被耗尽,天冬氨酸成为最终的能量来源。 N-乙酰天门冬氨酸浓度保持不变,表明在低血糖期间神经元/线粒体完整性得以保持。低血糖症的校正使PCr / Cr比正常化,并使氨基酸部分恢复至低血糖症前水平。代偿性神经化学变化在发育中的海马体长时间低血糖期间维持能量稳态。

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