Grape seed procyanidins administered at physiological doses to rats during pregnancy and lactation promote lipid oxidation and up-regulate AMPK in the muscle of male offspring in adulthood

被引:50
作者
Crescenti, Anna [1 ]
Maria del Bas, Josep [1 ]
Arola-Arnal, Anna [2 ]
Oms-Oliu, Gemma [3 ]
Arola, Lluis [2 ,4 ]
Caimari, Antoni [1 ]
机构
[1] CEICS, CTNS, TECNIO, GRNS, Reus 43204, Spain
[2] Univ Rovira & Virgili, Dept Bioquim & Biotecnol, Nutrigen Res Grp, E-43007 Tarragona, Spain
[3] Univ Lleida, Dept Food Technol, Lleida, Spain
[4] CEICS, CTNS, TECNIO, Reus 43204, Spain
关键词
Grape seed procyanidins; Metabolic programming; Skeletal muscle; Inflammation; AMPK; Lipid oxidation; ACTIVATED PROTEIN-KINASE; FATTY-ACID OXIDATION; MITOCHONDRIAL-FUNCTION; SUBSTRATE OXIDATION; METABOLIC SYNDROME; POLYPHENOLS; OBESITY; EXTRACT; FETAL; INFLAMMATION;
D O I
10.1016/j.jnutbio.2015.03.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of the present study was to test whether the administration of a grape seed procyanidin extract (GSPE) during pregnancy and lactation, at doses extrapolated to human consumption, programs male offspring toward improved metabolism in adulthood. For this purpose, female rats were fed a normal-fat diet (NFD) and treated with either GSPE (25 mg kg I of body weight/day) or vehicle during gestation and lactation. The metabolic programming effects of GSPE were evaluated in the male offspring fed NFD from 30 to 170 days of life. No changes were observed in body weight, adiposity, circulating lipid profile and insulin sensitivity between the offspring of dams treated with GSPE (STD-GSPE group) and their counterparts (STD-veh). However, the STD-GSPE offspring had lower circulating levels of C-reactive protein and lower respiratory quotient values, shifting whole-body energy catabolism from carbohydrate to fat oxidation. Furthermore, the STD-GSPE animals also exhibited increased levels of total and phosphorylated AMP-activated protein kinase (AMPK) and an over-expression of the mRNA levels of key genes related to fatty acid uptake (Fatp1 and CD36) and beta-oxidation (ppar alpha and had) in skeletal muscle. Our results indicate that GSPE programs healthy male offspring towards a better circulating inflammatory profile and greater lipid utilisation in adulthood. The metabolic programming effects of GSPE that are related to the enhancement of fatty acid oxidation in skeletal muscle seem to be mediated, at least in part, by AMPK. These findings could be of relevance in the prevention of pathologies associated to lifestyle and aging, such as obesity and insulin resistance. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:912 / 920
页数:9
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