内科学
内分泌学
医学
胰岛素
C肽
2型糖尿病
糖尿病
胰高血糖素
胰高血糖素样肽-1
肽
化学
生物化学
作者
M. Albareda,Mercedes Rigla,J Rodríguez-Espinosa,A Caballero,Ana Chico,R Cabezas,Gemma Carreras,Antonio Pérez
标识
DOI:10.1016/j.diabres.2004.10.005
摘要
Abstract
Aim:
The aim of this study was to determine whether the influence of insulin therapy on fasting and stimulated C-peptide levels in type 2 diabetic subjects is due to plasma glucose reduction or a direct effect of exogenous insulin. Methods:
Plasma glucose and serum C-peptide levels were determined before and after IV injection of 1mg glucagon on three separate days in 21 type 2 diabetic subjects. Day 1: without pharmacological treatment and fasting plasma glucose >11.1mmol/L; day 2: fasting plasma glucose 4.4–7.8mmol/L, 1h after withdrawing intravenous regular insulin infusion; day 3: fasting plasma glucose 4.4–7.8mmol/L with bed-time NPH insulin. Results:
Fasting and glucagon stimulated C-peptide levels were higher on day 1 than days 2 and 3. Fasting, but not stimulated C-peptide levels, were lower on day 3 than day 2. These differences were not appeared when the percentage of C-peptide increment or the C-peptide/glucose ratio were compared in the three days. Conclusions:
Blood glucose reduction instead of exogenous insulin is responsible for the C-peptide decrease during insulin therapy in type 2 diabetic subjects.
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