Signals adapting the beta cells to changes in insulin sensitivity

被引:5
作者
Ahrén, B [1 ]
Pacini, G [1 ]
机构
[1] Lund Univ, Dept Med, SE-22184 Lund, Sweden
来源
METABOLIC SYNDROME: DIABETES, OBESITY, HYPERLIPIDEMIA AND HYPERTENSION | 2003年 / 1253卷
关键词
insulin secretion; insulin sensitivity; islet adaptation; leptin; adiponectin;
D O I
10.1016/S0531-5131(02)01281-5
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Insulin sensitivity and secretion are related in a curvilinear inverse asymptotic function. However, the signaling factors mediating this relation are not known. In this study, we explored whether circulating glucose, lipids or two adipocyte-derived hormones, leptin and adiponectin, are related to the curvilinear function between insulin sensitivity and secretion in subjects with normal glucose tolerance. Thereby, insulin secretion (2-5-min insulin response to intravenous arginine) and insulin sensitivity (euglycemic, hyperinsulinemic clamp) were established in 68 healthy women, aged 61 years. We confirmed the curvilinear relation between insulin sensitivity and insulin secretion (r = -0.71, P < 0.001). To quantify the ability of the beta cells to secrete insulin for balancing a change in insulin sensitivity, we introduce the beta cell compensation index (BCI) by dividing insulin secretion by insulin sensitivity. This index correlated significantly with circulating triglycerides, leptin and adiponectin as well as BMI, but not fasting or 2-h glucose. A multivariate stepwise regression analysis using these variables as independent variables and lg BCI as the dependent variable revealed that leptin (r = 0.54, P < 0.001) and adiponectin (r = -0.33, P = 0.008) independently contributed to lg BCI (R-2 of the model = 0.19m, P = 0.038). The study, therefore, suggests that adipocyte-derived hormones contribute to the beta cell compensation to insulin resistance. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:105 / 113
页数:9
相关论文
共 24 条
[1]   Quantification of insulin secretion in relation to insulin sensitivity in nondiabetic postmenopausal women [J].
Ahrén, B ;
Larsson, H .
DIABETES, 2002, 51 :S202-S211
[2]   Impaired adaptation of first-phase insulin secretion in postmenopausal women with glucose intolerance [J].
Ahren, B ;
Pacini, G .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 1997, 273 (04) :E701-E707
[3]  
AHREN B, 1999, METABOLISM, V277, pR959
[4]   Accurate assessment of β-cell function -: The hyperbolic correction [J].
Bergman, RN ;
Ader, M ;
Huecking, K ;
Van Citters, G .
DIABETES, 2002, 51 :S212-S220
[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]   EFFECTS OF A 48-H FAT INFUSION ON INSULIN-SECRETION AND GLUCOSE-UTILIZATION [J].
BODEN, G ;
CHEN, XH ;
ROSNER, J ;
BARTON, M .
DIABETES, 1995, 44 (10) :1239-1242
[7]   INSULIN RESPONSE TO GLUCOSE INFUSION IN DIABETIC AND NON-DIABETIC MONOZYGOTIC TWIN PAIRS . GENETIC CONTROL OF INSULIN RESPONSE [J].
CERASI, E ;
LUFT, R .
ACTA ENDOCRINOLOGICA, 1967, 55 (02) :330-&
[8]   PATHOGENESIS OF NIDDM - A BALANCED OVERVIEW [J].
DEFRONZO, RA ;
BONADONNA, RC ;
FERRANNINI, E .
DIABETES CARE, 1992, 15 (03) :318-368
[9]  
DEFRONZO RA, 1979, AM J PHYSIOL, V237, pE214
[10]   The adipocyte:: a model for integration of endocrine and metabolic signaling in energy metabolism regulation [J].
Frühbeck, G ;
Gómez-Ambrosi, J ;
Muruzábal, FJ ;
Burrell, MA .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (06) :E827-E847