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应用磷-31 磁共振饱和传递波谱技术测量胰岛素输注对人体骨骼肌三磷酸腺苷转换率的急性效应。

Measuring the acute effect of insulin infusion on ATP turnover rate in human skeletal muscle using phosphorus-31 magnetic resonance saturation transfer spectroscopy.

机构信息

Institute of Cellular Medicine, Newcastle Magnetic Resonance Centre, Newcastle University, Newcastle upon Tyne, UK.

出版信息

NMR Biomed. 2010 Oct;23(8):952-7. doi: 10.1002/nbm.1519.

DOI:10.1002/nbm.1519
PMID:20623795
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3120981/
Abstract

Mitochondrial dysfunction has been proposed to underlie the insulin resistance of type 2 diabetes. However, the relative time course of insulin action in stimulating ATP turnover rate and glucose uptake in skeletal muscle has not been examined. These two parameters were measured in young healthy subjects using the (31)P MRS saturation transfer method in conjunction with the euglycaemic hyperinsulinaemic clamp technique respectively. Glucose infusion rate rose rapidly from 0 to 2.90 ± 0.11 mg/kg(ffm)/min during the first 10 min of insulin infusion and further to 6.17 ± 0.57 mg/kg(ffm)/min between 15 and 45 min. In contrast, baseline ATP turnover rate was 9.0 ± 0.4 µmol/g/min of muscle and did not change during the first 45 min of insulin infusion. Between 50 and 80 minutes ATP turnover rate increased by 8% and remained steady to 150 minutes (9.7 ± 0.5 µmol/g/min of muscle, p = 0.03 vs baseline). The in vivo time course of insulin stimulation of skeletal muscle ATP turnover rate is not consistent with a rate limiting effect upon the initiation of insulin-stimulated glycogen synthesis.

摘要

线粒体功能障碍被认为是 2 型糖尿病胰岛素抵抗的基础。然而,尚未研究胰岛素刺激骨骼肌中 ATP 周转率和葡萄糖摄取的相对时程。使用(31)P MRS 饱和转移方法结合正常血糖高胰岛素钳夹技术,分别在年轻健康受试者中测量了这两个参数。在胰岛素输注的最初 10 分钟内,葡萄糖输注率迅速从 0 上升到 2.90 ± 0.11 mg/kg(ffm)/min,在 15 至 45 分钟之间进一步上升到 6.17 ± 0.57 mg/kg(ffm)/min。相比之下,基线 ATP 周转率为 9.0 ± 0.4 µmol/g/min 的肌肉,在胰岛素输注的最初 45 分钟内没有变化。在 50 到 80 分钟之间,ATP 周转率增加了 8%,并保持稳定至 150 分钟(9.7 ± 0.5 µmol/g/min 的肌肉,p = 0.03 与基线相比)。胰岛素刺激骨骼肌 ATP 周转率的体内时程与胰岛素刺激糖原合成开始时的限速作用不一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/01179eb2ba81/nbm0023-0952-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/c511ea091f05/nbm0023-0952-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/c72088aa2fc2/nbm0023-0952-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/01179eb2ba81/nbm0023-0952-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/c511ea091f05/nbm0023-0952-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/c72088aa2fc2/nbm0023-0952-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2369/3120981/01179eb2ba81/nbm0023-0952-f3.jpg

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