Increased dietary fat attenuates the anorexic effects of intracerebroventricular injections of MTII

被引:53
作者
Clegg, DJ
Benoit, SC
Air, EL
Jackman, A
Tso, P
D'Alessio, D
Woods, SC
Seeley, RJ
机构
[1] Univ Cincinnati, Med Ctr, Dept Psychiat, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Med Ctr, Dept Biomed Sci & Cell Biol, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Med Ctr, Dept Pathol, Cincinnati, OH 45267 USA
[4] Univ Cincinnati, Med Ctr, Dept Med, Cincinnati, OH 45267 USA
[5] Procter & Gamble Pharmaceut, Cincinnati, OH 45040 USA
关键词
D O I
10.1210/en.2002-0218
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The hypothalamic melanocortin ( MC) system provides a critical inhibitory control on food intake and body weight. Because access to high-fat (HF) diets is associated with the development of obesity, we hypothesized that increased dietary fat attenuates signaling through the MC system. To evaluate this hypothesis, we compared the efficacy of the MC3/4 receptor agonist, MTII, to reduce food intake in rats fed carefully matched HF or low-fat (LF) diets for 12 wk. Rats given the HF diet ad libitum were significantly more obese than rats given the LF diet, and had significantly higher plasma insulin and leptin levels. MTII given into the third cerebral ventricle in doses of 0.1, 0.3, and 1.0 nmol was less effective at reducing food intake in HF rats than in LF rats. Whole-hypothalamic expression of the MC agonist precursor gene, proopiomelanocortin, the MC antagonist agouti-related protein, and the MC4 receptor, were not different between the HF and LF groups. These results indicate that consumption of a HF diet decreases signaling through the melanocortin system, an abnormality that could contribute to diet-induced obesity.
引用
收藏
页码:2941 / 2946
页数:6
相关论文
共 62 条
[21]   Coexpression of Agrp and NPY in fasting-activated hypothalamic neurons [J].
Hahn, TM ;
Breininger, JF ;
Baskin, DG ;
Schwartz, MW .
NATURE NEUROSCIENCE, 1998, 1 (04) :271-272
[22]   Changes in hypothalamic agouti-related protein (AGRP), but not α-MSH or pro-opiomelanocortin concentrations in dietary-obese and food-restricted rats [J].
Harrold, JA ;
Williams, G ;
Widdowson, PS .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 258 (03) :574-577
[23]  
Hayward MD, 2002, J NEUROSCI, V22, P8251
[24]   What to do about the metabolic syndrome? [J].
Hill, JO ;
Bessesen, D .
ARCHIVES OF INTERNAL MEDICINE, 2003, 163 (04) :395-397
[25]   Obesity and the environment: Where do we go from here? [J].
Hill, JO ;
Wyatt, HR ;
Reed, GW ;
Peters, JC .
SCIENCE, 2003, 299 (5608) :853-855
[26]   Environmental contributions to the obesity epidemic [J].
Hill, JO ;
Peters, JC .
SCIENCE, 1998, 280 (5368) :1371-1374
[27]   Targeted disruption of the melanocortin-4 receptor results in obesity in mice [J].
Huszar, D ;
Lynch, CA ;
FairchildHuntress, V ;
Dunmore, JH ;
Fang, Q ;
Berkemeier, LR ;
Gu, W ;
Kesterson, RA ;
Boston, BA ;
Cone, RD ;
Smith, FJ ;
Campfield, LA ;
Burn, P ;
Lee, F .
CELL, 1997, 88 (01) :131-141
[28]   Melanocortin-3 receptor mRNA expression in pro-opiomelanocortin neurones of the rat arcuate nucleus [J].
Jégou, S ;
Boutelet, I ;
Vaudry, H .
JOURNAL OF NEUROENDOCRINOLOGY, 2000, 12 (06) :501-505
[29]   Expression of melanocortin 4 receptor mRNA in the central nervous system of the rat [J].
Kishi, T ;
Aschkenasi, CJ ;
Lee, CE ;
Mountjoy, KG ;
Saper, CB ;
Elmquist, JK .
JOURNAL OF COMPARATIVE NEUROLOGY, 2003, 457 (03) :213-235
[30]   Varying body mass index cutoff points to describe overweight prevalence among US Adults: NHANES III (1988 to 1994) [J].
Kuczmarski, RJ ;
Carroll, MD ;
Flegal, KM ;
Troiano, RP .
OBESITY RESEARCH, 1997, 5 (06) :542-548