Effect of meta-chlorophenylpiperazine and cholecystokinin on food intake of Osborne-Mendel and S5B/P1 rats

Obesity (Silver Spring). 2007 Mar;15(3):624-31. doi: 10.1038/oby.2007.579.

Abstract

Objective: To investigate whether there is a difference in sensitivity to a serotonin agonist, meta-chlorophenylpiperazine (mCPP), or cholecystokinin (CCK-8), an intestinal hormone that inhibits food intake, between the Osborne-Mendel (OM) rat, which becomes obese eating a high-fat diet, and the S5B/Pl (S5B) rat, which is resistant to dietary-induced obesity.

Research methods and procedures: OM and S5B rats were adapted to either a high-saturated-fat diet (56% energy as fat) or a low-fat diet (10% energy as fat) or to both for 14 days and then treated with several doses of mCPP or CCK-8.

Results: Treatment with mCPP reduced food intake in both strains of rats. The dose-response curve showed that the OM rats had an increased sensitivity to the serotonergic agonist. Animals eating the high-fat diet had less response to mCPP; and in the S5B rats, the response was significantly reduced. After treatment with CCK-8, there was a similar dose-related suppression of food intake in both the OM and S5B rats.

Discussion: These data are consistent with the hypothesis that the serotonin system in the S5B rat has a greater activity that could act to inhibit fat intake. The response to CCK was not significantly affected by strain or diet.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cholecystokinin / pharmacology*
  • Diet, Atherogenic
  • Diet, Fat-Restricted
  • Dose-Response Relationship, Drug
  • Eating / drug effects*
  • Gastrointestinal Agents / pharmacology
  • Male
  • Piperazines / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Serotonin 5-HT2 Receptor Agonists

Substances

  • Gastrointestinal Agents
  • Piperazines
  • Serotonin 5-HT2 Receptor Agonists
  • Cholecystokinin
  • 1-(3-chlorophenyl)piperazine