Effects of nonglucose nutrients on insulin secretion and action in people with pre-diabetes

被引:35
作者
Bock, Gerlies
Man, Chiara Dalla
Campioni, Marco
Chittilapilly, Elizabeth
Basu, Rita
Toffolo, Gianna
Cobelli, Claudio
Rizza, Robert
机构
[1] Mayo Clin & Mayo Fdn, Coll Med, Div Endocrinol Diabet Metab & Nutr, Rochester, MN 55905 USA
[2] Univ Padua, Dept Elect & Informat, Padua, Italy
关键词
D O I
10.2337/db06-1272
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
To determine whether nonglucose nutrient-induced insulin secretion is impaired in pre-diabetes, subjects with impaired or normal fasting glucose were studied after ingesting either a mixed meal containing 75 g glucose or 75 g glucose alone. Despite comparable glucose areas above basal, glucose-induced insulin secretion was higher (P < 0.05) and insulin action lower (P < 0.05) during the meal than the oral glucose tolerance test (OGTT) in all subgroups regardless of whether they had abnormal or normal glucose tolerance (NGT). However, the nutrient-induced delta (meal minus OGTT) in insulin secretion and glucagon concentrations did not differ among groups. Furthermore, the decrease in insulin action after meal ingestion was compensated in all groups by an appropriate increase in insulin secretion resulting in disposition indexes during meals that were equal to or greater than those present during the OGTT. In contrast, disposition indexes were reduced (P < 0.01) during the OGTT in the impaired glucose tolerance groups, indicating that reduced glucose induced insulin secretion. We conclude that, whereas glucose-induced insulin secretion is impaired in people with abnormal glucose tolerance, nonglucose nutrient-induced secretion is intact, suggesting that a glucose-specific defect in the insulin secretory pathway is an early event in the evolution of type 2 diabetes.
引用
收藏
页码:1113 / 1119
页数:7
相关论文
共 52 条
[1]   Insulin secretion and action in subjects with impaired fasting glucose and impaired glucose tolerance - Results from the veterans administration genetic epidemiology study [J].
Abdul-Ghani, MA ;
Jenkinson, CP ;
Richardson, DK ;
Tripathy, D ;
DeFronzo, RA .
DIABETES, 2006, 55 (05) :1430-1435
[2]   Higher insulin concentrations are required to suppress gluconeogenesis than glycogenolysis in nondiabetic humans [J].
Adkins, A ;
Basu, R ;
Persson, M ;
Dicke, B ;
Shah, P ;
Vella, A ;
Schwenk, WF ;
Rizza, R .
DIABETES, 2003, 52 (09) :2213-2220
[3]   SAAM II: Simulation, Analysis, and Modeling Software for tracer and pharmacokinetic studies [J].
Barrett, PHR ;
Bell, BM ;
Cobelli, C ;
Golde, H ;
Schumitzky, A ;
Vicini, P ;
Foster, DM .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1998, 47 (04) :484-492
[4]   Mechanisms of the age-associated deterioration in glucose tolerance - Contribution of alterations in insulin secretion, action, and clearance [J].
Basu, R ;
Breda, E ;
Oberg, AL ;
Powell, CC ;
Dalla Man, C ;
Basu, A ;
Vittone, JL ;
Klee, GG ;
Arora, P ;
Jensen, MD ;
Toffolo, G ;
Cobelli, C ;
Rizza, RA .
DIABETES, 2003, 52 (07) :1738-1748
[5]   PHYSIOLOGIC EVALUATION OF FACTORS CONTROLLING GLUCOSE-TOLERANCE IN MAN - MEASUREMENT OF INSULIN SENSITIVITY AND BETA-CELL GLUCOSE SENSITIVITY FROM THE RESPONSE TO INTRAVENOUS GLUCOSE [J].
BERGMAN, RN ;
PHILLIPS, LS ;
COBELLI, C .
JOURNAL OF CLINICAL INVESTIGATION, 1981, 68 (06) :1456-1467
[6]   Pathogenesis of pre-diabetes - Mechanisms of fasting and postprandial hyperglycemia in people with impaired fasting glucose and/or impaired glucose tolerance [J].
Bock, Gerlies ;
Dalla Man, Chiara ;
Campioni, Marco ;
Chittilapilly, Elizabeth ;
Basu, Rita ;
Toffolo, Gianna ;
Cobelli, Claudio ;
Rizza, Robert .
DIABETES, 2006, 55 (12) :3536-3549
[7]   Effects of free fatty acids on gluconeogenesis and autoregulation of glucose production in type 2 diabetes [J].
Boden, G ;
Chen, XH ;
Capulong, E ;
Mozzoli, M .
DIABETES, 2001, 50 (04) :810-816
[8]   Free fatty acids in obesity and type 2 diabetes:: defining their role in the development of insulin resistance and β-cell dysfunction [J].
Boden, G ;
Shulman, GI .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 :14-23
[9]   Oral glucose tolerance test minimal model indexes of β-cell function and insulin sensitivity [J].
Breda, E ;
Cavaghan, MK ;
Toffolo, G ;
Polonsky, KS ;
Cobelli, C .
DIABETES, 2001, 50 (01) :150-158
[10]   RELATIONSHIPS BETWEEN FASTING PLASMA GLUCOSE LEVELS AND INSULIN-SECRETION DURING INTRAVENOUS GLUCOSE-TOLERANCE TESTS [J].
BRUNZELL, JD ;
ROBERTSON, RP ;
LERNER, RL ;
HAZZARD, WR ;
ENSINCK, JW ;
BIERMAN, EL ;
PORTE, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1976, 42 (02) :222-229