Effect of a high-fat diet on 24-h pattern of circulating levels of prolactin, luteinizing hormone, testosterone, corticosterone, thyroid-stimulating hormone and glucose, and pineal melatonin content, in rats

被引:93
作者
Cano, Pilar [1 ]
Jimenez-Ortega, Vanesa [1 ]
Larrad, Alvaro [1 ]
Reyes Toso, Carlos F. [2 ]
Cardinali, Daniel P. [2 ]
Esquifino, Ana I. [1 ]
机构
[1] Univ Complutense, Fac Med, Dept Bioquim & Biol Mol 3, E-28040 Madrid, Spain
[2] Univ Buenos Aires, Fac Med, Dept Fisiol, RA-1425 Buenos Aires, DF, Argentina
关键词
circadian; high-fat diet; obesity; hyperglycemia; melatonin; prolactin;
D O I
10.1007/s12020-008-9066-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Circadian rhythmicity is affected in obese subjects. This article analyzes the effect of a high-fat diet (35% fat) on 24-h changes circulating prolactin, luteinizing hormone (LH), testosterone, corticosterone, thyroid-stimulating hormone (TSH) and glucose, and pineal melatonin content, in rats. When body weight of rats reached the values of morbid obesity, the animals were sacrificed at six different time intervals throughout a 24-h cycle, together with age-matched controls fed a normal diet (4% fat). Plasma hormone levels were measured by specific radioimmunoassays and glucose concentration by an automated glucose oxidase method. In rats under a high-fat diet, a significant disruption of the 24-h pattern of plasma TSH, LH, and testosterone and a slight disruption of prolactin rhythm were found. Additionally, high-fat fed rats showed significantly lower total values of plasma TSH and testosterone and absence of correlation between testosterone and circulating LH levels. Plasma corticosterone levels increased significantly in high-fat fed rats and their 24-h variation became blunted. In obese animals, a significant hyperglycemia developed, individual plasma glucose values correlating with circulating corticosterone in high-fat fed rats only. The amplitude of the nocturnal pineal melatonin peak decreased significantly in high-fat fed rats. The results underlie the significant effects that obesity has on circadian organization of hormone secretion.
引用
收藏
页码:118 / 125
页数:8
相关论文
共 49 条
[1]   Resting energy expenditure is sensitive to small dose changes in patients on chronic thyroid hormone replacement [J].
AlAdsani, H ;
Hoffer, LJ ;
Silva, JE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) :1118-1125
[2]   Loss of nocturnal dipping of blood pressure and heart rate in obesity-induced hypertension in rabbits [J].
Antic, V ;
Van Vliet, BN ;
Montani, JP .
AUTONOMIC NEUROSCIENCE-BASIC & CLINICAL, 2001, 90 (1-2) :152-157
[3]   Seasonal changes in adiposity: the roles of the photoperiod, melatonin and other hormones, and sympathetic nervous system [J].
Bartness, TJ ;
Demas, GE ;
Song, CK .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2002, 227 (06) :363-376
[4]   Beyond energy balance: There is more to obesity than kilocalories [J].
Bray, GA ;
Champagne, CM .
JOURNAL OF THE AMERICAN DIETETIC ASSOCIATION, 2005, 105 (05) :S17-S23
[5]   High-fat diets:: Modeling the metabolic disorders of human obesity in rodents [J].
Buettner, Roland ;
Schoelmerich, Juergen ;
Bollheimer, L. Cornelius .
OBESITY, 2007, 15 (04) :798-808
[6]   Loss of diurnal rhythms of blood pressure and heart rate caused by high-fat feeding [J].
Carroll, JF ;
Thaden, JJ ;
Wright, AM ;
Strange, T .
AMERICAN JOURNAL OF HYPERTENSION, 2005, 18 (10) :1320-1326
[7]  
Cerf ME, 2007, MED SCI MONITOR, V13, pRA12
[8]   24-hour changes in circulating prolactin, follicle-stimulating hormone, luteinizing hormone, and testosterone in young male rats subjected to calorie restriction [J].
Chacon, F ;
Cano, P ;
Jimenez, V ;
Cardinali, DP ;
Marcos, A ;
Esquifino, AI .
CHRONOBIOLOGY INTERNATIONAL, 2004, 21 (03) :393-404
[9]   Development and application of rodent models for type 2 diabetes [J].
Chen, D ;
Wang, MW .
DIABETES OBESITY & METABOLISM, 2005, 7 (04) :307-317
[10]   EFFECT OF COLD-EXPOSURE AND NUTRIENT INTAKE ON SYMPATHETIC NERVOUS-SYSTEM ACTIVITY IN RAT-KIDNEY [J].
DALY, PA ;
YOUNG, JB ;
LANDSBERG, L .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 263 (04) :F586-F593