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正常人体短期和长期低血糖期间葡萄糖反向调节的比较。

Comparison of glucose counterregulation during short-term and prolonged hypoglycemia in normal humans.

作者信息

De Feo P, Perriello G, De Cosmo S, Ventura M M, Campbell P J, Brunetti P, Gerich J E, Bolli G B

出版信息

Diabetes. 1986 May;35(5):563-9.

PMID:2869997
Abstract

To compare glucose counterregulatory mechanisms during short-term hypoglycemia and prolonged hypoglycemia, insulin was infused either intravenously (160 mU X M-2 X min) for 10 min or subcutaneously (15 mU X M-2 X min) for 12 h in normal volunteers. With each type of insulin infusion, hypoglycemia (approximately 50 mg/dl) was either allowed to develop or was prevented (control experiments) by the glucose-clamp technique. During prolonged hypoglycemia, both increased glucose production (1.55 +/- 0.05 versus 0.33 +/- 0.14 mg X kg-1 X min in control experiments at 12 h, P less than 0.01) and suppressed glucose utilization (1.55 +/- 0.06 versus 3.17 +/- 0.15 mg X kg-1 X min in control studies at 12 h, P less than 0.01) were involved in counterregulation. During short-term hypoglycemia, only increased glucose production (3.23 +/- 0.33 versus 0.06 +/- 0.03 mg X kg-1 X min in control experiments at 60 min) was involved, since glucose clearance actually increased (3.99 +/- 0.20 versus 2.88 +/- 0.02 ml X kg-1 X min in control experiments at 60 min, P less than 0.01). Estimated portal venous insulin concentrations decreased 40% (basal 24 +/- 3 versus 14 +/- 1 mU/ml at 60 min, P less than 0.01) in the short-term hypoglycemia experiments but remained at basal levels (basal 25 +/- 1 versus approximately 26 microU/min between 1 and 12 h) during prolonged hypoglycemia. Despite the fact that hypoglycemia was more gradually induced in the prolonged hypoglycemia model, peak counterregulatory hormone responses were at least as great as those during short-term hypoglycemia.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为比较短期低血糖和长期低血糖期间的葡萄糖对抗调节机制,对正常志愿者静脉输注胰岛素(160 mU×M⁻²×min)10分钟或皮下输注胰岛素(15 mU×M⁻²×min)12小时。在每种胰岛素输注方式下,通过葡萄糖钳夹技术使低血糖(约50 mg/dl)发生或预防(对照实验)。在长期低血糖期间,葡萄糖生成增加(12小时对照实验中为1.55±0.05对0.33±0.14 mg×kg⁻¹×min,P<0.01)和葡萄糖利用受抑制(12小时对照研究中为1.55±0.06对3.17±0.15 mg×kg⁻¹×min,P<0.01)均参与对抗调节。在短期低血糖期间,仅葡萄糖生成增加(60分钟对照实验中为3.23±0.33对0.06±0.03 mg×kg⁻¹×min),因为葡萄糖清除率实际上增加了(60分钟对照实验中为3.99±0.20对2.88±0.02 ml×kg⁻¹×min,P<0.01)。在短期低血糖实验中,估计的门静脉胰岛素浓度降低了40%(基础值24±3对60分钟时的14±1 mU/ml,P<0.01),但在长期低血糖期间保持在基础水平(基础值25±1对1至12小时期间约26 μU/min)。尽管在长期低血糖模型中低血糖诱导更为缓慢,但对抗调节激素的峰值反应至少与短期低血糖期间一样大。(摘要截短于250字)

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