Resveratrol treatment rescues hyperleptinemia and improves hypothalamic leptin signaling programmed by maternal high-fat diet in rats

被引:64
作者
Franco, J. G. [1 ]
Dias-Rocha, C. P. [1 ]
Fernandes, T. P. [1 ]
Albuquerque Maia, L. [2 ]
Lisboa, P. C. [2 ]
Moura, E. G. [2 ]
Pazos-Moura, C. C. [1 ]
Trevenzoli, I. H. [1 ]
机构
[1] Univ Fed Rio de Janeiro, Mol Endocrinol Lab, Inst Biofis Carlos Chagas Filho, Av Carlos Chagas Filho 373,Sl G0-16,Cidade Univ, BR-21941902 Rio De Janeiro, RJ, Brazil
[2] Univ Estado Rio de Janeiro, Lab Fisiol Endocrina, Dept Ciencias Fisiol, Inst Biol Roberto Alcantara Gomes, BR-20550011 Rio De Janeiro, Brazil
关键词
Obesity; Leptin; Programming; Resveratrol; ADULT RATS; RESISTANCE; MECHANISMS; EXPRESSION; PARAMETERS; SECRETION; NUTRITION; RECEPTOR; OBESITY; YOUNG;
D O I
10.1007/s00394-015-0880-7
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 [营养与食品卫生学];
摘要
Perinatal high-fat diet is associated with obesity and metabolic diseases in adult offspring. Resveratrol has been shown to exert antioxidant and anti-obesity actions. However, the effects of resveratrol on leptinemia and leptin signaling are still unknown as well as whether resveratrol treatment can improve metabolic outcomes programmed by maternal high-fat diet. We hypothesize that resveratrol treatment in male rats programmed by high-fat diet would decrease body weight and food intake, and leptinemia with changes in central leptin signaling. Female Wistar rats were divided into two groups: control group (C), which received a standard diet containing 9 % of the calories as fat, and high-fat group (HF), which received a diet containing 28 % of the calories as fat. Dams were fed in C or HF diet during 8 weeks before mating and throughout gestation and lactation. C and HF male offspring received standard diet throughout life. From 150 until 180 days of age, offspring received resveratrol (30 mg/Kg body weight/day) or vehicle (carboxymethylcellulose). HF offspring had increased body weight, hyperphagia and increased subcutaneous and visceral fat mass compared to controls, and resveratrol treatment decreased adiposity. HF offspring had increased leptinemia as well as increased SOCS3 in the arcuate nucleus of the hypothalamus, which suggest central leptin resistance. Resveratrol treatment rescued leptinemia and increased p-STAT3 content in the hypothalamus with no changes in SOCS3, suggesting improvement in leptin signaling. Collectively, our data suggest that resveratrol could reverse hyperleptinemia and improve central leptin action in adult offspring from HF mothers attenuating obesity.
引用
收藏
页码:601 / 610
页数:10
相关论文
共 39 条
[1]
Mechanisms underlying current and future anti-obesity drugs [J].
Adan, Roger A. H. .
TRENDS IN NEUROSCIENCES, 2013, 36 (02) :133-140
[2]
Resveratrol: Anti-Obesity Mechanisms of Action [J].
Aguirre, Leixuri ;
Fernandez-Quintela, Alfredo ;
Arias, Noemi ;
Portillo, Maria P. .
MOLECULES, 2014, 19 (11) :18632-18655
[3]
Adipokines and the peripheral and neural control of energy balance [J].
Ahima, Rexford S. ;
Lazar, Mitchell A. .
MOLECULAR ENDOCRINOLOGY, 2008, 22 (05) :1023-1031
[4]
Digging deeper into obesity [J].
Ahima, Rexford S. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) :2076-2079
[5]
Changes in white adipose tissue metabolism induced by resveratrol in rats [J].
Alberdi, Goiuri ;
Rodriguez, Victor M. ;
Miranda, Jonatan ;
Macarulla, Maria T. ;
Arias, Noemi ;
Andres-Lacueva, Cristina ;
Portillo, Maria P. .
NUTRITION & METABOLISM, 2011, 8
[6]
Obesity and early life [J].
Barker, D. J. P. .
OBESITY REVIEWS, 2007, 8 :45-49
[7]
Resveratrol supplementation improves white adipose tissue function in a depot-specific manner in Zucker diabetic fatty rats [J].
Beaudoin, Marie-Soleil ;
Snook, Laelie A. ;
Arkell, Alicia M. ;
Simpson, Jeremy A. ;
Holloway, Graham P. ;
Wright, David C. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2013, 305 (05) :R542-R551
[8]
Bjorbæk C, 2009, J INVEST MED, V57, P789, DOI 10.2310/JIM.0b013e3181bb0d49
[9]
Developmental programming of hypothalamic feeding circuits [J].
Bouret, S. G. ;
Simerly, R. B. .
CLINICAL GENETICS, 2006, 70 (04) :295-301
[10]
Bouret SG, 2010, NESTLE NUTR WORKS SE, V65, P25, DOI 10.1159/000281143