» Articles » PMID: 25152240

Grape Seed Procyanidin Supplementation to Rats Fed a High-fat Diet During Pregnancy and Lactation Increases the Body Fat Content and Modulates the Inflammatory Response and the Adipose Tissue Metabolism of the Male Offspring in Youth

Overview
Specialty Endocrinology
Date 2014 Aug 26
PMID 25152240
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Objective: Procyanidins are polyphenolic bioactive compounds that exert beneficial effects against obesity and its related diseases. The aim of this study was to evaluate whether supplementation with low doses of a grape seed procyanidin extract (GSPE) to rats during pre- and postnatal periods provides biological effects to their offspring in youth.

Design: The metabolic programming effect of GSPE was evaluated in the 30-day-old male offspring of four groups of rats that were fed either a standard diet (STD) or a high-fat diet (HFD) and that were supplemented with either GSPE (25 mg kg(-1) of body weight per day) or vehicle during pregnancy and lactation.

Results: Significant increases in the adiposity index and in the weights of all the white adipose tissue depots studied (retroperitoneal, mesenteric, epididymal (EWAT) and inguinal) were observed in the offspring of rats that were fed a HFD and that were treated with GSPE (HFD-GSPE group) compared with the offspring of rats that were fed the same diet but that did not receive the procyanidins (HFD group). The HFD-GSPE animals also exhibited a higher number of cells in the EWAT, a sharp decrease in the circulating levels of monocyte chemoattractant protein-1 (MCP-1) and a moderate decrease in the plasma glycerol levels. The transcriptomic analysis performed in the EWAT showed 238 genes that were differentially expressed between the HFD and the HFD-GSPE animals, most of which were associated with the immune function and the inflammatory response, in addition to genes associated with adipose tissue remodeling and function, lipid and glucose homeostasis and the metabolism of methyl groups.

Conclusion: The GSPE treatment in rats that were fed an HFD during pregnancy and lactation induced a clear metabolic programming effect in the offspring, increasing adiposity, decreasing the circulating levels of MCP-1 and changing the gene expression in the EWAT toward a better inflammatory profile.

Citing Articles

Maternal Polyphenols and Offspring Cardiovascular-Kidney-Metabolic Health.

Tain Y, Hsu C Nutrients. 2024; 16(18).

PMID: 39339768 PMC: 11434705. DOI: 10.3390/nu16183168.


Early Life Programming of Adipose Tissue Remodeling and Browning Capacity by Micronutrients and Bioactive Compounds as a Potential Anti-Obesity Strategy.

Bonet M, Ribot J, Sanchez J, Palou A, Pico C Cells. 2024; 13(10.

PMID: 38786092 PMC: 11120104. DOI: 10.3390/cells13100870.


Maternal Supplementation with a Cocoa Extract during Lactation Deeply Modulates Dams' Metabolism, Increases Adiponectin Circulating Levels and Improves the Inflammatory Profile in Obese Rat Offspring.

Marine-Casado R, Domenech-Coca C, Crescenti A, Rodriguez Gomez M, Del Bas J, Arola L Nutrients. 2022; 14(23).

PMID: 36501173 PMC: 9738144. DOI: 10.3390/nu14235134.


The postnatal window is critical for the development of sex-specific metabolic and gut microbiota outcomes in offspring.

Daoust L, Choi B, Lacroix S, Vilela V, Varin T, Dudonne S Gut Microbes. 2021; 13(1):2004070.

PMID: 34812123 PMC: 8632343. DOI: 10.1080/19490976.2021.2004070.


Proanthocyanidins and Where to Find Them: A Meta-Analytic Approach to Investigate Their Chemistry, Biosynthesis, Distribution, and Effect on Human Health.

Mannino G, Chinigo G, Serio G, Genova T, Gentile C, Munaron L Antioxidants (Basel). 2021; 10(8).

PMID: 34439477 PMC: 8389005. DOI: 10.3390/antiox10081229.


References
1.
Rouault C, Pellegrinelli V, Schilch R, Cotillard A, Poitou C, Tordjman J . Roles of chemokine ligand-2 (CXCL2) and neutrophils in influencing endothelial cell function and inflammation of human adipose tissue. Endocrinology. 2013; 154(3):1069-79. DOI: 10.1210/en.2012-1415. View

2.
Del Bas J, Ricketts M, Vaque M, Sala E, Quesada H, Ardevol A . Dietary procyanidins enhance transcriptional activity of bile acid-activated FXR in vitro and reduce triglyceridemia in vivo in a FXR-dependent manner. Mol Nutr Food Res. 2009; 53(7):805-14. PMC: 4142053. DOI: 10.1002/mnfr.200800364. View

3.
Williams K, Schalinske K . Tissue-specific alterations of methyl group metabolism with DNA hypermethylation in the Zucker (type 2) diabetic fatty rat. Diabetes Metab Res Rev. 2011; 28(2):123-31. DOI: 10.1002/dmrr.1281. View

4.
Barrett T, Wilhite S, Ledoux P, Evangelista C, Kim I, Tomashevsky M . NCBI GEO: archive for functional genomics data sets--update. Nucleic Acids Res. 2012; 41(Database issue):D991-5. PMC: 3531084. DOI: 10.1093/nar/gks1193. View

5.
Panee J . Monocyte Chemoattractant Protein 1 (MCP-1) in obesity and diabetes. Cytokine. 2012; 60(1):1-12. PMC: 3437929. DOI: 10.1016/j.cyto.2012.06.018. View