Standard light breakfast inhibits circulating ghrelin level to the same extent of oral glucose load in humans, despite different impact on glucose and insulin levels

被引:21
作者
Gottero, C
Bellone, S
Rapa, A
van Koetsveld, P
Vivenza, D
Prodam, F
Benso, A
Destefanis, S
Gauna, C
Bellone, J
Hofland, L
van der Lely, AJ
Bona, G
Ghigo, E
Broglio, F
机构
[1] Univ Turin, Dept Internal Med, Div Endocrinol, Turin, Italy
[2] Regina Margherita Children Hosp, Div Pediat Endocrinol, Turin, Italy
[3] Univ Piemonte Orientale, Dept Med Sci, Pediat Unit, Novara, Italy
[4] Erasmus Univ, Dept Internal Med, Div Endocrinol, Rotterdam, Netherlands
关键词
ghrelin; breakfast; oral glucose load; food intake;
D O I
10.1007/BF03349158
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Ghrelin levels are increased by fasting and energy restriction, decreased by food intake, glucose load and insulin but not by lipids and amino acids. Accordingly, ghrelin levels are elevated in anorexia and cachexia and reduced in obesity. Herein we compared the effects of a standardized light breakfast (SLB) on morning circulating ghrelin levels with those of oral glucose load (OGTT) in normal subjects. Specifically, 8 young adult volunteers [age (mean +/- SEM): 28.0 +/- 2.0 yr; body mass index (BMI): 22.4 +/- 0.6 kg/m(2)] underwent the following testing sessions: a) OGTT (1100 g po at 0 min, about 400 kcal); b) SLB (about 400 kcal, 45% carbohydrates, 13% proteins and 42% lipids at 0 min) on three different days; c) placebo (100 ml water po). In all sessions, at baseline, blood samples were withdrawn twice at 5-min interval to characterize the inter- and intra-individual reproducibility of the variables assayed. After placebo and OGTT, blood samples were withdrawn every 15 min up to +120 min. After SLB, blood samples were taken at 60 min only. Ghrelin, insulin and glucose levels were assayed at each time point in all sessions. Similarly to insulin and glucose levels, at baseline, ghrelin showed remarkable intra-subject reproducibility both in the same sessions and among the different sessions. Placebo did not significantly modify ghrelin, insulin and glucose. OGTT increased (p<0.01) glucose (baseline vs peak: 80.0 +/- 3.6 vs 140.5 +/- 6.3 mg/dl) and insulin (20.2 +/- 6.2 vs 115.3 +/- 10.3 mU/l) levels. SLB increased (p<0.05) both insulin (16.3 +/- 1.8 vs 48.3 +/- 6.3 mU/l) and glucose (74.5 +/- 3.7 vs 82.9 +/- 3.1 mg/dl) levels. Notably both the insulin and glucose increases after OGTT were significantly higher (p<0.01) than that induced by SLB. After OGTT, ghrelin levels underwent a significant reduction (baseline vs nadir: 355.7 +/- 150.8 vs 243.3 +/- 98.8 pg/ml; p<0.05) reaching the nadir at time +60 min. Similarly, ghrelin levels 60 min after SLB (264.8 +/- 44.8 pg/ml) were significantly (p<0.01) lower than at baseline (341.4 +/- 54.9 pg/ml). No significant differences in the reduction of ghrelin levels after OGTT and SLB were observed. In conclusion, these findings show that light breakfast inhibits ghrelin secretion to the same extent of OGTT in adults despite lower variations in glucose and insulin levels. (C) 2003, Editrice Kurtis.
引用
收藏
页码:1203 / 1207
页数:5
相关论文
共 19 条
[1]   Stomach is a major source of circulating ghrelin, and feeding state determines plasma ghrelin-like immunoreactivity levels in humans [J].
Ariyasu, H ;
Takaya, K ;
Tagami, T ;
Ogawa, Y ;
Hosoda, K ;
Akamizu, T ;
Suda, M ;
Koh, T ;
Natsui, K ;
Toyooka, S ;
Shirakami, G ;
Usui, T ;
Shimatsu, A ;
Doi, K ;
Hosoda, H ;
Kojima, M ;
Kangawa, K ;
Nakao, K .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (10) :4753-4758
[2]   Ghrelin, macronutrient intake and dietary preferences in Long-Evans rats [J].
Beck, B ;
Musse, N ;
Stricker-Krongrad, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 292 (04) :1031-1035
[3]  
Broglio F, 2002, J PEDIATR ENDOCR MET, V15, P1219
[4]   Ghrelin and the endocrine pancreas [J].
Broglio, F ;
Gottero, C ;
Benso, A ;
Prodam, F ;
Volante, M ;
Destefanis, S ;
Gauna, C ;
Muccioli, G ;
Papotti, M ;
van der Lely, AJ ;
Ghigo, E .
ENDOCRINE, 2003, 22 (01) :19-24
[5]   Genetics and pathophysiology of human obesity [J].
Cummings, DE ;
Schwartz, MW .
ANNUAL REVIEW OF MEDICINE, 2003, 54 :453-471
[6]   A preprandial rise in plasma ghrelin levels suggests a role in meal initiation in humans [J].
Cummings, DE ;
Purnell, JQ ;
Frayo, RS ;
Schmidova, K ;
Wisse, BE ;
Weigle, DS .
DIABETES, 2001, 50 (08) :1714-1719
[7]   The tissue distribution of the mRNA of ghrelin and subtypes of its receptor, GHS-R, in humans [J].
Gnanapavan, S ;
Kola, B ;
Bustin, SA ;
Morris, DG ;
McGee, P ;
Fairclough, P ;
Bhattacharya, S ;
Carpenter, R ;
Grossman, AB ;
Korbonits, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2988-2991
[8]   Ghrelin: discovery of the natural endogenous ligand for the growth hormone secretagogue receptor [J].
Kojima, M ;
Hosoda, H ;
Matsuo, H ;
Kangawa, K .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2001, 12 (03) :118-122
[9]   Ghrelin, a new gastrointestinal endocrine peptide that stimulates insulin secretion: Enteric distribution, ontogeny, influence of endocrine, and dietary manipulations [J].
Lee, HM ;
Wang, GY ;
Englander, EW ;
Kojima, M ;
Greeley, GH .
ENDOCRINOLOGY, 2002, 143 (01) :185-190
[10]   Ghrelin is not necessary for adequate hormonal counterregulation of insulin-induced hypoglycemia [J].
Lucidi, P ;
Murdolo, G ;
Di Loreto, C ;
De Cicco, A ;
Parlanti, N ;
Fanelli, C ;
Santeusanio, F ;
Bolli, GB ;
De Feo, P .
DIABETES, 2002, 51 (10) :2911-2914