Plasma ghrelin concentration and energy balance:: Overfeeding and negative energy balance studies in twins

被引:128
作者
Ravussin, E
Tschöp, M
Morales, S
Bouchard, C
Heiman, ML
机构
[1] Pennington Biomed Res Ctr, Baton Rouge, LA 70808 USA
[2] Eli Lilly & Co, Lilly Res Labs, Endocrine Res, Indianapolis, IN 46285 USA
关键词
D O I
10.1210/jc.86.9.4547
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Central (intracerebral ventral) and peripheral (subcutaneous and intraperitoneal) administration of ghrelin causes obesity in rodents by increasing food intake and decreasing fat oxidation. Recent studies in humans have shown that plasma ghrelin concentration was inversely related to body fat and was lower in Pima Indians, a population susceptible to obesity. Whether ghrelin plays a role in the etiology of obesity in humans is unknown. We, therefore, measured plasma ghrelin concentration before and after two interventions in monozygotic twins previously studied at Laval University, Quebec City. Twelve pairs of monozygotic twins were overfed by 84,000 kcal over a 100-day period, whereas another seven pairs of monozygotic twins were submitted to a 53,000 kcal negative energy balance induced by exercise over a 93-day period. At baseline, for all the subjects, plasma ghrelin concentration was negatively correlated with body mass and body fatness (r varying from 0.36 to 0.45). The intraclass coefficient for the twin resemblance (r(1) = 0.75; p = 0.006) indicated that plasma ghrelin concentration is a familial trait. In response to the 100-day intervention, plasma ghrelin exhibited a non-significant decrease of 61 +/- 130 fmol/l (p = 0.18) with overfeeding and a non-significant increase of 58 +/- 34 fmol/l (p = 0.17) with negative energy balance. However, there was no relationship between baseline plasma ghrelin concentration and the magnitude of body weight change in both interventions. These first experimental data under "clamped energy balance conditions" do not provide evidence that plasma ghrelin is involved in the etiology of human obesity. However, studies in free-living individuals are needed to clarify this question.
引用
收藏
页码:4547 / 4551
页数:5
相关论文
共 21 条
[1]   Preliminary evidence that Ghrelin, the natural GH secretagogue (GHS)-receptor ligand, strongly stimulates GH secretion in humans [J].
Arvat, E ;
Di Vito, L ;
Broglio, F ;
Papotti, M ;
Muccioli, G ;
Dieguez, C ;
Casanueva, FF ;
Deghenghi, R ;
Camanni, F ;
Ghigo, E .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2000, 23 (08) :493-495
[2]   Ghrelin is an appetite-stimulatory signal from stomach with structural resemblance to motilin [J].
Asakawa, A ;
Inui, A ;
Kaga, T ;
Yuzuriha, H ;
Nagata, T ;
Ueno, N ;
Makino, S ;
Fujimiya, M ;
Niijima, A ;
Fujino, MA ;
Kasuga, M .
GASTROENTEROLOGY, 2001, 120 (02) :337-345
[3]   THE RESPONSE TO LONG-TERM OVERFEEDING IN IDENTICAL-TWINS [J].
BOUCHARD, C ;
TREMBLAY, A ;
DESPRES, JP ;
NADEAU, A ;
LUPIEN, PJ ;
THERIAULT, G ;
DUSSAULT, J ;
MOORJANI, S ;
PINAULT, S ;
FOURNIER, G .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (21) :1477-1482
[4]  
Bouchard C, 1994, Obes Res, V2, P400
[5]   Ghrelin, a novel growth hormone-releasing acylated peptide, is synthesized in a distinct endocrine cell type in the gastrointestinal tracts of rats and humans [J].
Date, Y ;
Kojima, M ;
Hosoda, H ;
Sawaguchi, A ;
Mondal, MS ;
Suganuma, T ;
Matsukura, S ;
Kangawa, K ;
Nakazato, M .
ENDOCRINOLOGY, 2000, 141 (11) :4255-4261
[6]   Ghrelin, a novel placental-derived hormone [J].
Gualillo, O ;
Caminos, JE ;
Blanco, M ;
Garcìa-Caballero, T ;
Kojima, M ;
Kangawa, K ;
Dieguez, C ;
Casanueva, FF .
ENDOCRINOLOGY, 2001, 142 (02) :788-794
[7]   Distribution of mRNA encoding the growth hormone secretagogue receptor in brain and peripheral tissues [J].
Guan, XM ;
Yu, H ;
Palyha, OC ;
McKee, KK ;
Feighner, SD ;
Sirinathsinghji, DJS ;
Smith, RG ;
VanderPloeg, LHT ;
Howard, AD .
MOLECULAR BRAIN RESEARCH, 1997, 48 (01) :23-29
[8]   Central effect of ghrelin, an endogenous growth hormone secretagogue, on hypothalamic peptide gene expression [J].
Kamegai, J ;
Tamura, H ;
Shimizu, T ;
Ishii, S ;
Sugihara, H ;
Wakabayashi, I .
ENDOCRINOLOGY, 2000, 141 (12) :4797-4800
[9]   Ghrelin is a growth-hormone-releasing acylated peptide from stomach [J].
Kojima, M ;
Hosoda, H ;
Date, Y ;
Nakazato, M ;
Matsuo, H ;
Kangawa, K .
NATURE, 1999, 402 (6762) :656-660
[10]   The expression of the growth hormone secretagogue receptor ligand ghrelin in normal and abnormal human pituitary and other neuroendocrine tumors [J].
Korbonits, M ;
Bustin, SA ;
Kojima, M ;
Jordan, S ;
Adams, EF ;
Lowe, DG ;
Kangawa, K ;
Grossman, AB .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (02) :881-887