Differential responses of circulating ghrelin to high-fat or high-carbohydrate meal in healthy women

被引:179
作者
Monteleone, P [1 ]
Bencivenga, R [1 ]
Longobardi, N [1 ]
Serritella, C [1 ]
Maj, M [1 ]
机构
[1] Univ Naples Federico II, SUN, Dept Psychiat, I-80138 Naples, Italy
关键词
D O I
10.1210/jc.2003-030797
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The effects of specific nutritional factors on ghrelin secretion have not been investigated in humans. Therefore, we assessed ghrelin responses to a high-carbohydrate meal (1217 kcal with 77% carbohydrates, 10% protein, and 13% lipids) and to an isocaloric high-fat meal (15% carbohydrates, 10% proteins, and 75% lipids) in 14 nonobese healthy women. Eleven subjects also rated their hunger feelings on visual analog scales. Circulating ghrelin abruptly fell after both meals, but, after the carbohydrate meal, its maximum percent decrease was significantly greater than after the fat meal ( P = 0.02). Plasma insulin and glucose levels rose after the meals, but their increases were significantly higher after the carbohydrate meal than after the fat meal. No significant change was observed in circulating leptin after both meals. Moreover, compared with the fat meal, the carbohydrate meal had a significantly greater suppressant effect on hunger feelings. Plasma ghrelin changes were significantly associated with hunger changes (P < 0.007). These findings show that circulating ghrelin is differently suppressed by diet manipulations. The mechanisms responsible for such a phenomenon and its possible implication in the physiology of human satiety remain to be elucidated.
引用
收藏
页码:5510 / 5514
页数:5
相关论文
共 25 条
[1]  
[Anonymous], BMDP STAT SOFTWARE
[2]   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
[3]   Insulin, unlike food intake, does not suppress ghrelin in human subjects. [J].
Caixás, A ;
Bashore, C ;
Nash, W ;
Pi-Sunyer, FX ;
Laferrère, B .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (04) :1902-1906
[4]   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
[5]   Food fails to suppress ghrelin levels in obese humans [J].
English, PJ ;
Ghatei, MA ;
Malik, IA ;
Bloom, SR ;
Wilding, JPH .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (06) :2984-2987
[6]   The influence of insulin on circulating ghrelin [J].
Flanagan, DE ;
Evans, ML ;
Monsod, TP ;
Rife, F ;
Heptulla, RA ;
Tamborlane, WV ;
Sherwin, RS .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 284 (02) :E313-E316
[7]   A satiety quotient: A formulation to assess the satiating effect of food [J].
Green, SM ;
Delargy, HJ ;
Joanes, D ;
Blundell, JE .
APPETITE, 1997, 29 (03) :291-304
[8]   Purification and characterization of rat des-Gln14-ghrelin, a second endogenous ligand for the growth hormone secretagogue receptor [J].
Hosoda, H ;
Kojima, M ;
Matsuo, H ;
Kangawa, K .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (29) :21995-22000
[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]  
Möhlig M, 2002, J ENDOCRINOL INVEST, V25, pRC36