Literature DB >> 20172705

Feeding conditions control the expression of genes involved in sterol metabolism in peripheral blood mononuclear cells of normoweight and diet-induced (cafeteria) obese rats.

Antoni Caimari1, Paula Oliver, Wendy Rodenburg, Jaap Keijer, Andreu Palou.   

Abstract

Peripheral blood mononuclear cells (PBMC) are easily obtainable cells from blood whose gene expression profiles have been proven to be highly robust in distinguishing a disease state from healthy state. Sterol metabolism is of physiological importance, and although its nutritional response in liver has been described, it is poorly studied in PBMC. To examine if PBMC sterol metabolism reflects diet-induced physiological responses, we analysed the whole genome gene expression response of PBMC and focused on sterol metabolism-related genes affected by different feeding conditions (ad libitum feeding, fasting, and refeeding) in normoweight (control) rats and in diet-induced (cafeteria) obese rats. Our results of microarray analysis show that, in control rats, 21 genes involved in sterol metabolism were regulated by the different feeding conditions, whereas in cafeteria-obese rats, only seven genes showed a changed expression. Most of the genes identified were classified into three pathways: sterol biosynthesis, cholesterol transport and uptake and sterol signaling. The expression profile of these genes was similar to that previously described for liver, decreasing in response to fasting conditions and recovering the levels found in fed animals after 6-h-refeeding. In addition, our data and the comparable expression pattern of sterol metabolism-related genes between PBMC and liver suggest similar sterol regulatory element-binding protein-mediated regulatory mechanisms in response to feeding conditions in both tissues. In conclusion, the expression of genes involved in sterol metabolism is highly controlled by feeding conditions in PBMC of control rats, but this control is impaired in cafeteria-obese animals. The pathophysiological significance of this impairment requires further investigation.
Copyright © 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20172705     DOI: 10.1016/j.jnutbio.2009.10.001

Source DB:  PubMed          Journal:  J Nutr Biochem        ISSN: 0955-2863            Impact factor:   6.048


  12 in total

1.  The intake of a high-fat diet and grape seed procyanidins induces gene expression changes in peripheral blood mononuclear cells of hamsters: capturing alterations in lipid and cholesterol metabolisms.

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Authors:  J Sánchez; C Picó; W Ahrens; R Foraita; A Fraterman; L A Moreno; P Russo; A Siani; A Palou
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3.  The intake of high-fat diets induces the acquisition of brown adipocyte gene expression features in white adipose tissue.

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Journal:  Int J Obes (Lond)       Date:  2015-06-11       Impact factor: 5.095

4.  Cafeteria diet overfeeding in young male rats impairs the adaptive response to fed/fasted conditions and increases adiposity independent of body weight.

Authors:  H Castro; C A Pomar; C Picó; J Sánchez; A Palou
Journal:  Int J Obes (Lond)       Date:  2014-07-21       Impact factor: 5.095

5.  Effects of Ethanolic Extract of Cynara cardunculus (Artichoke) Leaves on Neuroinflammatory and Neurochemical Parameters in a Diet-Induced Mice Obesity Model.

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6.  Peripheral blood mononuclear cells: a potential source of homeostatic imbalance markers associated with obesity development.

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Authors:  Jaap Keijer; Femke P M Hoevenaars; Arie Nieuwenhuizen; Evert M van Schothorst
Journal:  Nutrients       Date:  2014-10-21       Impact factor: 5.717

9.  Whole Blood RNA as a Source of Transcript-Based Nutrition- and Metabolic Health-Related Biomarkers.

Authors:  Petar D Petrov; M Luisa Bonet; Bárbara Reynés; Paula Oliver; Andreu Palou; Joan Ribot
Journal:  PLoS One       Date:  2016-05-10       Impact factor: 3.240

10.  Graviola (Annona muricata) attenuates behavioural alterations and testicular oxidative stress induced by streptozotocin in diabetic rats.

Authors:  Abdel-Wahab A Alsenosy; Ali H El-Far; Kadry M Sadek; Safinaz A Ibrahim; Mustafa S Atta; Ahmed Sayed-Ahmed; Soad K Al Jaouni; Shaker A Mousa
Journal:  PLoS One       Date:  2019-09-11       Impact factor: 3.240

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