Behavioral and Metabolic Effects of a Calorie-Restricted Cafeteria Diet and Oleuropein Supplementation in Obese Male Rats

Nutrients. 2021 Dec 15;13(12):4474. doi: 10.3390/nu13124474.

Abstract

Diet-induced obesity models are widely used to investigate dietary interventions for treating obesity. This study was aimed to test whether a dietary intervention based on a calorie-restricted cafeteria diet (CAF-R) and a polyphenolic compound (Oleuropein, OLE) supplementation modified sucrose intake, preference, and taste reactivity in cafeteria diet (CAF)-induced obese rats. CAF diet consists of high-energy, highly palatable human foods. Male rats fed standard chow (STD) or CAF diet were compared with obese rats fed CAF-R diet, alone or supplemented with an olive tree leaves extract (25 mg/kg*day) containing a 20.1% of OLE (CAF-RO). Biometric, food consumption, and serum parameters were measured. CAF diet increased body weight, food and energy consumption and obesity-associated metabolic parameters. CAF-R and CAF-RO diets significantly attenuated body weight gain and BMI, diminished food and energy intake and improved biochemical parameters such as triacylglycerides and insulin resistance which did not differ between CAF-RO and STD groups. The three cafeteria groups diminished sucrose intake and preference compared to STD group. CAF-RO also diminished the hedonic responses for the high sucrose concentrations compared with the other groups. These results indicate that CAF-R diet may be an efficient strategy to restore obesity-associated alterations, whilst OLE supplementation seems to have an additional beneficial effect on sweet taste function.

Keywords: diet-induced obesity; energy restriction; food intake; hedonic response; leptin; polyphenols; sucrose preference; sweet taste.

MeSH terms

  • Animals
  • Anti-Infective Agents / pharmacology
  • Behavior, Animal / drug effects*
  • Caloric Restriction*
  • Dietary Supplements*
  • Dose-Response Relationship, Drug
  • Eating
  • Energy Metabolism / drug effects*
  • Iridoid Glucosides / pharmacology*
  • Male
  • Obesity / therapy*
  • Rats
  • Rats, Sprague-Dawley
  • Sucrose / administration & dosage
  • Sucrose / pharmacology

Substances

  • Anti-Infective Agents
  • Iridoid Glucosides
  • oleuropein
  • Sucrose