Cafeteria diet induces global and Slc27a3-specific hypomethylation in male Wistar rats

Adipocyte. 2021 Dec;10(1):108-118. doi: 10.1080/21623945.2021.1886697.

Abstract

Increased visceral adipose tissue (VAT) is associated with metabolic dysfunction, while subcutaneous adipose tissue (SAT) is considered protective. The mechanisms underlying these differences are not fully elucidated. This study aimed to investigate molecular differences in VAT and SAT of male Wistar rats fed a cafeteria diet (CD) or a standard rodent diet (STD) for three months. The expression of fatty acid metabolism genes was analysed by quantitative real-time PCR. Global and gene-specific DNA methylation was quantified using the Imprint® Methylated DNA Quantification Kit and pyrosequencing, respectively. Bodyweight, retroperitoneal fat mass, insulin resistance, leptin and triglyceride concentrations and adipocyte hypertrophy were higher in CD- compared to STD-fed rats. The expression of solute carrier family 27 member 3 (Slc27a3), a fatty acid transporter, was 9.6-fold higher in VAT and 6.3-fold lower in SAT of CD- versus STD-fed rats. Taqman probes confirmed increased Slc27a3 expression, while pyrosequencing showed Slc27a3 hypomethylation in VAT of CD- compared to STD-fed rats. The CD decreased global methylation in both VAT and SAT, although no depot differences were observed. Dysregulated fatty acid influx in VAT, in response to a CD, provides insight into the mechanisms underlying depot-differences in adipose tissue expansion during obesity and metabolic disease. Abbreviations: CD: cafeteria diet; E2F1: E2F Transcription Factor 1; EMSA: electrophoretic mobility shift assay; EGFR: epidermal growth factor receptor; GCF: GC-Rich Sequence DNA-Binding Factor; HOMA-IR: Homeostasis model for insulin resistance; NKX2-1: NK2 homeobox 1; PCR: Polymerase chain reaction; qRT-PCR: quantitative real-time PCR; RF: retroperitoneal fat; SAT: subcutaneous adipose tissue; Slc27a3: solute carrier family 27 member 3; STD: standard diet; TNFα: tumour necrosis factor alpha; TTS: transcriptional start site; T2D: Type 2 Diabetes; VAT: visceral adipose tissue; WT1 I: Wilms' tumour protein 1.

Keywords: DNA methylation; Obesity; Slc27a3; adipose tissue; insulin resistance; subcutaneous; visceral.

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Body Weight
  • DNA Methylation / drug effects*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diet
  • Diet, High-Fat / adverse effects
  • Fatty Acid Transport Proteins / drug effects
  • Fatty Acid Transport Proteins / metabolism
  • Insulin / metabolism
  • Insulin Resistance / genetics
  • Intra-Abdominal Fat / metabolism*
  • Intra-Abdominal Fat / physiology
  • Leptin / metabolism
  • Male
  • Metabolic Diseases / metabolism
  • Metabolic Diseases / physiopathology
  • Obesity / metabolism
  • Rats
  • Rats, Wistar
  • Subcutaneous Fat / metabolism*
  • Subcutaneous Fat / physiology

Substances

  • Fatty Acid Transport Proteins
  • Insulin
  • Leptin

Grants and funding

This work was supported by the South African Medical Research Council (SAMRC) and The National Research Foundation professional development programme (PDP) [Grant number: 104987 awarded to CP and TW]. The content hereof is the sole responsibility of the authors and do not necessary represent the official views of the SAMRC or the funders.