Roux-en-Y Gastric Bypass and Caloric Restriction but Not Gut Hormone-Based Treatments Profoundly Impact the Hypothalamic Transcriptome in Obese Rats

Nutrients. 2021 Dec 28;14(1):116. doi: 10.3390/nu14010116.

Abstract

Background: The hypothalamus is an important brain region for the regulation of energy balance. Roux-en-Y gastric bypass (RYGB) surgery and gut hormone-based treatments are known to reduce body weight, but their effects on hypothalamic gene expression and signaling pathways are poorly studied.

Methods: Diet-induced obese male Wistar rats were randomized into the following groups: RYGB, sham operation, sham + body weight-matched (BWM) to the RYGB group, osmotic minipump delivering PYY3-36 (0.1 mg/kg/day), liraglutide s.c. (0.4 mg/kg/day), PYY3-36 + liraglutide, and saline. All groups (except BWM) were kept on a free choice of high- and low-fat diets. Four weeks after interventions, hypothalami were collected for RNA sequencing.

Results: While rats in the RYGB, BWM, and PYY3-36 + liraglutide groups had comparable reductions in body weight, only RYGB and BWM treatment had a major impact on hypothalamic gene expression. In these groups, hypothalamic leptin receptor expression as well as the JAK-STAT, PI3K-Akt, and AMPK signaling pathways were upregulated. No significant changes could be detected in PYY3-36 + liraglutide-, liraglutide-, and PYY-treated groups.

Conclusions: Despite causing similar body weight changes compared to RYGB and BWM, PYY3-36 + liraglutide treatment does not impact hypothalamic gene expression. Whether this striking difference is favorable or unfavorable to metabolic health in the long term requires further investigation.

Keywords: PYY3-36; Roux-en-Y gastric bypass surgery; hypothalamic gene expression; liraglutide; obesity.

MeSH terms

  • Animals
  • Body Weight
  • Caloric Restriction
  • Disease Models, Animal
  • Energy Metabolism
  • Gastric Bypass
  • Gastrointestinal Hormones / pharmacology*
  • Gene Expression / drug effects
  • Hypothalamus / metabolism*
  • Liraglutide / pharmacology*
  • Male
  • Obesity
  • Peptide Fragments / pharmacology*
  • Peptide YY / pharmacology*
  • Rats
  • Rats, Wistar
  • Signal Transduction / drug effects
  • Transcriptome / drug effects*

Substances

  • Gastrointestinal Hormones
  • Peptide Fragments
  • Peptide YY
  • peptide YY (3-36)
  • Liraglutide