Nocturnal free fatty acids are uniquely elevated in the longitudinal development of diet-induced insulin resistance and hyperinsulinemia

被引:74
作者
Kim, Stella P. [1 ]
Catalano, Karyn J. [1 ]
Hsu, Isabel R. [1 ]
Chiu, Jenny D. [1 ]
Richey, Joyce M. [1 ]
Bergman, Richard N. [1 ]
机构
[1] Univ So Calif, Keck Sch Med, Dept Physiol & Biophys, Los Angeles, CA 90033 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM | 2007年 / 292卷 / 06期
关键词
obesity; diurnal;
D O I
10.1152/ajpendo.00669.2006
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Obesity is strongly associated with hyperinsulinemia and insulin resistance, both primary risk factors for type 2 diabetes. It has been thought that increased fasting free fatty acids ( FFA) may be responsible for the development of insulin resistance during obesity, causing an increase in plasma glucose levels, which would then signal for compensatory hyperinsulinemia. But when obesity is induced by fat feeding in the dog model, there is development of insulin resistance and a marked increase in fasting insulin despite constant fasting FFA and glucose. We examined the 24- h plasma profiles of FFA, glucose, and other hormones to observe any potential longitudinal postprandial or nocturnal alterations that could lead to both insulin resistance and compensatory hyperinsulinemia induced by a high- fat diet in eight normal dogs. We found that after 6 wk of a high- fat, hypercaloric diet, there was development of significant insulin resistance and hyperinsulinemia as well as accumulation of both subcutaneous and visceral fat without a change in either fasting glucose or postprandial glucose. Moreover, although there was no change in fasting FFA, there was a highly significant increase in the nocturnal levels of FFA that occurred as a result of fat feeding. Thus enhanced nocturnal FFA, but not glucose, may be responsible for development of insulin resistance and fasting hyperinsulinemia in the fat- fed dog model.
引用
收藏
页码:E1590 / E1598
页数:9
相关论文
共 47 条
[1]   ACUTE PHARMACOLOGICAL BLOCKADE OF LIPOLYSIS NORMALIZES NOCTURNAL GROWTH-HORMONE LEVELS AND PULSATILITY IN OBESE SUBJECTS [J].
ANDREOTTI, AC ;
LANZI, R ;
MANZONI, MF ;
CAUMO, A ;
MORESCHI, A ;
PONTIROLI, AE .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (10) :1207-1213
[2]   Paradoxical decrease of an adipose-specific protein, adiponectin, in obesity [J].
Arita, Y ;
Kihara, S ;
Ouchi, N ;
Takahashi, M ;
Maeda, K ;
Miyagawa, J ;
Hotta, K ;
Shimomura, I ;
Nakamura, T ;
Miyaoka, K ;
Kuriyama, H ;
Nishida, M ;
Yamashita, S ;
Okubo, K ;
Matsubara, K ;
Muraguchi, M ;
Ohmoto, Y ;
Funahashi, T ;
Matsuzawa, Y .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (01) :79-83
[3]  
ARNER P, 1988, DIABETES METAB REV, V4, P507
[4]  
Balent B, 2002, ANN NY ACAD SCI, V967, P535
[5]   Central nervous system origins of the sympathetic nervous system outflow to white adipose tissue [J].
Bamshad, M ;
Aoki, VT ;
Adkison, MG ;
Warren, WS ;
Bartness, TJ .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1998, 275 (01) :R291-R299
[6]  
BJORNTORP P, 1969, ACTA MED SCAND, V185, P351
[7]   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
[8]  
Boden Guenther, 1998, Frontiers in Bioscience, V3, pD169
[9]   OOPSEG - A DATA SMOOTHING PROGRAM FOR QUANTITATION AND ISOLATION OF RANDOM MEASUREMENT ERROR [J].
BRADLEY, DC ;
STEIL, GM ;
BERGMAN, RN .
COMPUTER METHODS AND PROGRAMS IN BIOMEDICINE, 1995, 46 (01) :67-77
[10]   Restoration of adiponectin pulsatility in severely obese subjects after weight loss [J].
Calvani, M ;
Scarfone, A ;
Granato, L ;
Mora, EV ;
Nanni, G ;
Castagneto, M ;
Greco, AV ;
Manco, M ;
Mingrone, G .
DIABETES, 2004, 53 (04) :939-947