Non-sulfated cholecystokinin-8 reduces meal size and prolongs the intermeal interval in male Sprague Dawley rats

Neuropeptides. 2019 Feb:73:57-65. doi: 10.1016/j.npep.2018.11.003. Epub 2018 Nov 13.

Abstract

The current study measured seven feeding responses by non-sulfated cholecystokinin-8 (NS CCK-8) in freely fed adult male Sprague Dawley rats. The peptide (0, 0.5, 1, 3, 5 and 10 nmol/kg) was given intraperitoneally (ip) prior to the onset of the dark cycle, and first meal size (MS), second meal size, intermeal interval (IMI) length, satiety ratio (SR = IMI/MS), latency to first meal, duration of first meal, number of meals and 24-hour food intake were measured. We found that NS CCK-8 (0.5 and 1.0 nmol/kg) reduced MS, prolonged IMI length and increased SR during the dark cycle. Furthermore, the specific CCK-B receptor antagonist L365, 260 (1 mg/kg, ip) attenuated these responses. These results support a possible role for NS CCK-8 in regulating food intake.

Keywords: Devazepide; Food intake; L365,260; Non-sulfated CCK; Sulfated CCK.

MeSH terms

  • Animals
  • Cholecystokinin / pharmacology*
  • Eating / drug effects*
  • Feeding Behavior / drug effects*
  • Male
  • Meals*
  • Peptide Fragments / pharmacology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Peptide Fragments
  • cholecystokinin 8
  • Cholecystokinin