Murine hepatic proteome adaptation to high-fat diets with different contents of saturated fatty acids and linoleic acid : α-linolenic acid polyunsaturated fatty acid ratios

Author:

Liput Kamila P.12ORCID,Lepczyński Adam3ORCID,Poławska Ewa1ORCID,Ogłuszka Magdalena1ORCID,Starzyński Rafał1ORCID,Urbański Paweł1ORCID,Nawrocka Agata1ORCID,Jończy Aneta1ORCID,Pierzchała Dorota4,Pareek Chandra S.56,Gołyński Marcin56,Woźniakowski Grzegorz56ORCID,Czarnik Urszula7,Pierzchała Mariusz1ORCID

Affiliation:

1. Department of Institute of Genetics and Animal Biotechnology of the Polish Academy of Sciences, Jastrzębiec , Magdalenka , Poland

2. Institute of Biochemistry and Biophysics of the Polish Academy of Sciences , Warsaw , Poland

3. Department of Physiology, Cytobiology and Proteomics, West Pomeranian University of Technology , Szczecin , Poland

4. Maria Skłodowska-Curie National Research Institute of Oncology , Warsaw , Poland

5. Department of Infectious and Invasive Diseases and Veterinary Administration, Institute of Veterinary Medicine, Faculty of Biological and Veterinary Sciences, Nicolaus Copernicus University , Toruń , Poland

6. Division of Functional Genomics in Biological and Biomedical Research, Centre for Modern Interdisciplinary Technologies, Nicolaus Copernicus University , Toruń , Poland

7. Department of Pig Breeding, Faculty of Animal Bio-Engineering, University of Warmia and Mazury in Olsztyn , Olsztyn , Poland

Abstract

Abstract Introduction Some health disorders, such as obesity and type 2 diabetes, are associated with a poor diet and low quality of the fat in it. The type and duration of the diet have an impact on the liver. This investigation uses the proteomic approach to identify changes in the mouse liver protein profile in adaptation to high-fat diets with different saturated fatty acid contents and linoleic acid (18:2n-6) to α-linolenic acid (18:3n-3) fatty acid ratios. Material and Methods Four groups of male mice were fed different diets: one standard diet and three high-fat diets were investigated. After six months on these diets, the animals were sacrificed for liver dissection. Two-dimensional electrophoresis was used to separate the complex liver protein mixture, which enabled the separation of proteins against a wide, 3–10 range of pH and molecular weights of 15–250 kDa. Protein profiles were analysed in the PDQuest Advanced 8.0.1 program. Differentially expressed spots were identified using matrix-assisted laser desorption/ionisation–time-of-flight tandem mass spectrometry and peptide mass fingerprinting. The levels of identified proteins were validated using Western blotting. Transcript levels were evaluated using a real-time quantitative PCR. Results The analysis of mouse liver protein profiles enabled the identification of 32 protein spots differing between nutritional groups. Conclusion A diet high in polyunsaturated fatty acids modulated the levels of liver proteins involved in critical metabolic pathways, including amino acid metabolism, carbohydrate metabolism and cellular response to oxidative stress.

Publisher

Walter de Gruyter GmbH

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