Toward a Medical Gastric Bypass: Chronic Feeding Studies With Liraglutide + PYY3-36 Combination Therapy in Diet-Induced Obese Rats

Front Endocrinol (Lausanne). 2021 Jan 22:11:598843. doi: 10.3389/fendo.2020.598843. eCollection 2020.

Abstract

Background: Combination therapies of anorectic gut hormones partially mimic the beneficial effects of bariatric surgery. Thus far, the effects of a combined chronic systemic administration of Glucagon-like peptide-1 (GLP-1) and peptide tyrosine tyrosine 3-36 (PYY3-36) have not been directly compared to Roux-en-Y gastric bypass (RYGB) in a standardized experimental setting.

Methods: High-fat diet (HFD)-induced obese male Wistar rats were randomized into six treatment groups: (1) RYGB, (2) sham-operation (shams), (3) liraglutide, (4) PYY3-36, (5) PYY3-36+liraglutide (6), saline. Animals were kept on a free choice high- and low-fat diet. Food intake, preference, and body weight were measured daily for 4 weeks. Open field (OP) and elevated plus maze (EPM) tests were performed.

Results: RYGB reduced food intake and achieved sustained weight loss. Combined PYY3-36+liraglutide treatment led to similar and plateaued weight loss compared to RYGB. Combined PYY3-36+liraglutide treatment was superior to PYY3-36 (p ≤ 0.0001) and liraglutide (p ≤ 0.05 or p ≤ 0.01) mono-therapy. PYY3-36+liraglutide treatment and RYGB also reduced overall food intake and (less pronounced) high-fat preference compared to controls. The animals showed no signs of abnormal behavior in OF or EPM.

Conclusions: Liraglutide and PYY3-36 combination therapy vastly mimics reduced food intake, food choice and weight reducing benefits of RYGB.

Keywords: gastric bypass; liraglutide; obesity; peptide tyrosine tyrosine (PYY); peptide tyrosine tyrosine 3-36 (PYY3-36); rygb; treatment.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Body Weight
  • Combined Modality Therapy
  • Diet, High-Fat / adverse effects*
  • Eating*
  • Food Preferences
  • Gastric Bypass / methods*
  • Hypoglycemic Agents / pharmacology
  • Liraglutide / pharmacology*
  • Male
  • Obesity / etiology
  • Obesity / pathology
  • Obesity / therapy*
  • Peptide YY / pharmacology*
  • Rats
  • Rats, Wistar

Substances

  • Hypoglycemic Agents
  • Peptide YY
  • Liraglutide