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1 型糖尿病伴无症状性低血糖患者脑糖原含量和代谢。

Brain glycogen content and metabolism in subjects with type 1 diabetes and hypoglycemia unawareness.

机构信息

Department of Radiology, Center for Magnetic Resonance Research, Medical School, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

J Cereb Blood Flow Metab. 2012 Feb;32(2):256-63. doi: 10.1038/jcbfm.2011.138. Epub 2011 Oct 5.

Abstract

Supercompensated brain glycogen may contribute to the development of hypoglycemia unawareness in patients with type 1 diabetes by providing energy for the brain during periods of hypoglycemia. Our goal was to determine if brain glycogen content is elevated in patients with type 1 diabetes and hypoglycemia unawareness. We used in vivo (13)C nuclear magnetic resonance spectroscopy in conjunction with [1-(13)C]glucose administration in five patients with type 1 diabetes and hypoglycemia unawareness and five age-, gender-, and body mass index-matched healthy volunteers to measure brain glycogen content and metabolism. Glucose and insulin were administered intravenously over ∼51 hours at a rate titrated to maintain a blood glucose concentration of 7 mmol/L. (13)C-glycogen levels in the occipital lobe were measured at ∼5, 8, 13, 23, 32, 37, and 50 hours, during label wash-in and wash-out. Newly synthesized glycogen levels were higher in controls than in patients (P<0.0001) for matched average blood glucose and insulin levels, which may be due to higher brain glycogen content or faster turnover in controls. Metabolic modeling indicated lower brain glycogen content in patients than in controls (P=0.07), implying that glycogen supercompensation does not contribute to the development of hypoglycemia unawareness in humans with type 1 diabetes.

摘要

超补偿的大脑糖原可能通过在低血糖期间为大脑提供能量,从而导致 1 型糖尿病患者出现低血糖意识障碍。我们的目的是确定 1 型糖尿病伴低血糖意识障碍患者的大脑糖原含量是否升高。我们使用体内 (13)C 核磁共振波谱结合 [1-(13)C] 葡萄糖给药,在五名 1 型糖尿病伴低血糖意识障碍患者和五名年龄、性别和体重指数匹配的健康志愿者中测量大脑糖原含量和代谢。葡萄糖和胰岛素以静脉输注的方式给药,约 51 小时,输注速度滴定以维持血糖浓度为 7 mmol/L。在标记物洗脱期,在约 5、8、13、23、32、37 和 50 小时测量枕叶中的 (13)C-糖原水平。在匹配的平均血糖和胰岛素水平下,对照者的新合成糖原水平高于患者(P<0.0001),这可能是由于对照者的大脑糖原含量较高或周转率较快。代谢模型表明患者的大脑糖原含量低于对照者(P=0.07),这意味着糖原超补偿不会导致 1 型糖尿病患者出现低血糖意识障碍。

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