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在人类中,肝糖原分解对血浆胰高血糖素浓度生理性升高时葡萄糖生成的贡献。

Contribution of hepatic glycogenolysis to glucose production in humans in response to a physiological increase in plasma glucagon concentration.

作者信息

Magnusson I, Rothman D L, Gerard D P, Katz L D, Shulman G I

机构信息

Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8020.

出版信息

Diabetes. 1995 Feb;44(2):185-9. doi: 10.2337/diab.44.2.185.

Abstract

The contribution of net hepatic glycogenolysis to overall glucose production during a physiological increment in the plasma glucagon concentration was measured in six healthy subjects (18-24 years, 68-105 kg) after an overnight fast. Glucagon (approximately 3 ng.kg-1.min-1), somatostatin (0.1 microgram.kg-1.min-1), and insulin (0.9 pmol.kg-1.min-1) were infused for 3 h. Liver glycogen concentration was measured at 15-min intervals during this period using 13C-labeled nuclear magnetic resonance spectroscopy, and liver volume was assessed from magnetic resonance images. The rate of net hepatic glycogenolysis was calculated from the decrease in liver glycogen concentration over time, multiplied by the liver volume. The rate of glucose appearance (Ra) was calculated from [3-3H]glucose turnover data using a two-compartment model of glucose kinetics. Plasma glucagon concentration rose from 136 +/- 18 to 304 +/- 57 ng/l and plasma glucose concentration rose from 5.6 +/- 0.1 to 10.4 +/- 0.9 mmol/l on initiation of the infusions. Mean baseline Ra was 11.8 +/- 0.4 mumol.kg-1.min-1, increased rapidly after the beginning of the infusions, reaching its highest value after 20-40 min, and returned to baseline by 140 min. Liver glycogen concentration decreased almost linearly (from 300 +/- 19 mmol/l liver at baseline to 192 +/- 20 mmol/l liver at t = 124 min) during 2 h after the beginning of the infusions, and the calculated mean rate of net hepatic glycogenolysis was 21.7 +/- 3.6 mumol.kg-1.min-1. Mean Ra during the same time period was 22.8 +/- 2.3 mumol.kg-1.min-1. Thus, net hepatic glycogenolysis accounted for 93 +/- 9% of Ra.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在6名健康受试者(年龄18 - 24岁,体重68 - 105千克)过夜禁食后,测量血浆胰高血糖素浓度生理性升高期间肝脏净糖原分解对总体葡萄糖生成的贡献。输注胰高血糖素(约3纳克·千克⁻¹·分钟⁻¹)、生长抑素(0.1微克·千克⁻¹·分钟⁻¹)和胰岛素(0.9皮摩尔·千克⁻¹·分钟⁻¹)3小时。在此期间,每隔15分钟使用¹³C标记的核磁共振波谱法测量肝脏糖原浓度,并根据磁共振图像评估肝脏体积。肝脏净糖原分解速率根据肝脏糖原浓度随时间的下降计算得出,再乘以肝脏体积。葡萄糖出现率(Ra)使用葡萄糖动力学的双室模型根据[3 - ³H]葡萄糖周转数据计算得出。输注开始时,血浆胰高血糖素浓度从136±18纳克/升升至304±57纳克/升,血浆葡萄糖浓度从5.6±0.1毫摩尔/升升至10.4±0.9毫摩尔/升。平均基线Ra为11.8±0.4微摩尔·千克⁻¹·分钟⁻¹,输注开始后迅速升高,在20 - 40分钟后达到最高值,并在140分钟时恢复到基线。输注开始后2小时内,肝脏糖原浓度几乎呈线性下降(从基线时的300±19毫摩尔/升肝脏降至t = 124分钟时的192±20毫摩尔/升肝脏),计算得出的肝脏净糖原分解平均速率为21.7±3.6微摩尔·千克⁻¹·分钟⁻¹。同一时间段内的平均Ra为22.8±2.3微摩尔·千克⁻¹·分钟⁻¹。因此,肝脏净糖原分解占Ra的93±9%。(摘要截断于250字)

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